Open AccessReview

The Genus Broussonetia: An Updated Review of Phytochemistry, Pharmacology and Applications

Yueru Chen

^†,

Lu Wang

^†,

Xue Liu

Fulin Wang

Ying An

Wei Zhao

Jinli Tian

Degang Kong

Wenru Zhang

Yang Xu

Yahui Ba

and

Honglei Zhou

College of Pharmacy, Shandong University of Traditional Chinese Medicine, Jinan 250355, China

Author to whom correspondence should be addressed.

^†

These authors contributed equally to this work.

Molecules 2022, 27(16), 5344; https://doi.org/10.3390/molecules27165344

Submission received: 8 July 2022 / Revised: 15 August 2022 / Accepted: 18 August 2022 / Published: 22 August 2022

(This article belongs to the Section Natural Products Chemistry)

Download

Browse Figures

Versions Notes

Abstract

The Broussonetia genus (Moraceae), recognized for its value in many Chinese traditional herbs, mainly includes Broussonetia papyrifera (L.) L’Hér. ex Vent. (BP), Broussonetia kazinoki Siebold (BK), and Broussonetia luzonica (Blanco) Bureau (BL). Hitherto, researchers have found 338 compounds isolated from BP, BK, and BL, which included flavonoids, polyphenols, phenylpropanoids, alkaloids, terpenoids, steroids, and others. Moreover, its active compounds and extracts have exhibited a variety of pharmacological effects such as antitumor, antioxidant, anti-inflammatory, antidiabetic, anti-obesity, antibacterial, and antiviral properties, and its use against skin wrinkles. In this review, the phytochemistry and pharmacology of Broussonetia are updated systematically, after its applications are first summarized. In addition, this review also discusses the limitations of investigations and the potential direction of Broussonetia. This review can help to further understand the phytochemistry, pharmacology, and other applications of Broussonetia, which paves the way for future research.

Keywords:

Broussonetia; phytochemistry; pharmacology; applications

1. Introduction

Broussonetia is one of the most significant genera in the Moraceae family, a member of the Urticales order. The genus is composed of eleven species, comprising Broussonetia papyrifera (BP) (see Figure 1) [1], Broussonetia kazinoki (BK) (see Figure 2) [2], Broussonetia zeylanica (Thwaites) Corner (BZ) [3], Broussonetia luzonica (Blanco) Bureau (BL) [4], Broussonetia rupicola F.T. Wang and Tang (BR), Broussonetia kurzii (Hook.f.) Corner (BKU), Broussonetia kaempferi Siebold (BKA) [5], Broussonetia integrifolia Buch.-Ham. (BI), Broussonetia harmandii Gagnep. (BHG), Broussonetia × hanjiana M.Kim (BHM), and Broussonetia greveana (Baill.) C.C.Berg (BG) [6]. The various Broussonetia species have been an excellent source of conventional medicine to treat different diseases. Their roots, barks, fruits, and leaves have all been used in conventional medicine. In China, the leaves have been used to treat chronic prostatitis as a folk medicine [7], as well as for bleeding [8]. The bark could be used for special recipes [8]. The fruits have been confirmed to treat impotence and ophthalmic diseases [7], while the hematochrome from the fruits could be used as a foodstuff in history [9]. In the traditions of Tonga, Fiji, and Samoa, BP, a fibrous tree, was the main raw material used to make tapa cloth [10]. Moreover, one of the Broussonetia species was used by Cai Lun to create paper, one of the four great inventions of ancient China. Broussonetia species were also used as woody forage in ancient history [11].

According to the publication, Flora of China [12], the morphology of the genus is described thus: “Trees or shrubs, or vine-like shrubs; there is emulsion, and the winter buds are small. Leaves are alternate, split or non-divided, with serrated margins, basal veins triangular, lateral pinnate veins, and lateral leaves, detached, ovate lanceolate, early fall. The flowers are hermaphroditic or identical; the male flowers are drooping soft inflorescences or spherical cephalic inflorescences, the flowers are indumental, 4 or 3 lobes, the stamens and the flowers are fissured in the same number, folded inward at the time of flower buds, the degenerated stamens are small; the female flowers are densely spherical head-shaped inflorescences, bracts are stick-like, sustenance, flower tube-shaped, apical 3–4 lobes or full margins, succumbs, ovary hidden, stalked, pedunculate lateral, linear, ovules hanging from the ventricular roof. Polyflora is spherical, the embryo is curved, the cotyledons are rounded, flattened, or folded. The genus is distributed in eastern Asia and Pacific islands”.

The diversity of the chemical structures and pharmacological effects has attracted the interest of a variety of researchers. The genus of Broussonetia has been found to present 338 compounds, including flavonoids, polyphenols, alkaloids, terpenoids, steroids, and others. Active compounds isolated from Broussonetia have been demonstrated to have several biological properties, including antitumor [2], antioxidant [13], anti-inflammation [14], antidiabetic [15], anti-obesity [16], antibacterial [17], and antiviral activities [18], as well as being used for skin whitening [19] and against skin wrinkles, as well as many other uses. In terms of representative applications, Broussonetia species could be used as forage for cattle, Hu rams and lambs, growing goats, and other animals because of the high content of protein and fiber [20,21]. In addition, BP, combined with Lonicera japonica, may be used to treat inflammatory disorders [22]. Liquid bandages that include Styela clava tunics and BK bark cellulose powders could be used to heal cutaneous wounds [23].

This review efforts to provide comprehensive and up-to-date information on the Broussonetia genus, based on published references, focusing on phytochemistry, pharmacology, and several other applications. We also discuss the limitations of current research into Broussonetia. This review may provide a reference for researchers around the world to investigate and explore the potential applications of the Broussonetia genus.

2. Phytochemistry

According to the published references, outstanding results have been acquired by a variety of researchers when studying the stems, leaves, barks, radices, fruits, and whole plants of the Broussonetia genus. In total, 338 compounds have been isolated from BP, BK, and BL of the Broussonetia genus; these compounds consist of 144 flavonoids, 50 penylpropanoids, 38 polyphenols, 35 alkaloids, 17 terpenoids, 5 steroids, and 49 other metabolites. Their chemical structures have been elucidated using the nuclear magnetic resonance spectrometer (NMR) and mass spectrum (MS), along with comparisons with the published data. Their presence might be responsible for the biological properties of the various Broussonetia species. However, bioactive compounds that have been confirmed are scarce, the emphasis being on their crude extracts, leading to limitations in the finding of potential candidates for the treatment of corresponding diseases. Given the fact that abundant phytochemicals have been identified, their structure–activity relationships should be unraveled via numerous assays in the future, which will be conducive to unlocking the answers on how phytochemicals develop as targeted bioactive molecules.

2.1. Flavonoids

Compounds where the basic core is 2-phenylchromone are classified as flavonoids. Flavones are the main compounds in the 144 flavonoids extracted from Broussonetia species. Flavonoids, as primary bioactive compounds, demonstrated the most pharmacological properties, such as antitumor, antioxidant, anti-inflammatory, anti-diabetic, anti-obesity, antibacterial, and antiviral effects, along with skin whitening and anti-wrinkle properties, as well as other activities. In 1994, a new isoprenylated aurone, compound 76, and a novel isoprenylated flavan, compound 18, together with the known compounds 38, 40, 60, and 61, were isolated and characterized from the cortex of BP [24]. In 1995, Fang et al. [25] described how two new isoprenylated flavonols, compounds 49 and 51, were isolated and characterized from the root bark of BP. In 1996, Lin et al. [26] reported the presence of compounds 52, 142, 143, and 144 using two-dimensional techniques. A new prenylflavan, compound 37, and the known compounds 119 and 120 were isolated from the root barks of BK, and these compounds were evaluated for cytotoxic activity against several different cell lines [27]. In 2001, an in vitro aromatase inhibition assay was conducted by Lee et al. [28], and the results showed that the novel compounds 59, 26, 75, and 46, as well as the known compounds 47, 48, 50, 139, and 140, were found to be active as aromatase inhibitors, while compounds 56, 58, and 63 were inactive. Zhang et al. [29] described, for the first time, five new diprenylated flavonols, compounds 45, 100, 136, 137, and 138, which were obtained from an ethanolic extract of the leaves of BK; they evaluated the cytotoxic activities of these compounds. In 2002, two new compounds, 71 and 135, were isolated from the roots of BP and the structures were determined using spectroscopy; moreover, compound 71 exhibited significantly inhibitory activities against the PTP1B enzyme [30]. In 2008, the structure of a novel compound, 126, together with compounds 15, 16, 20, 27, 69, 70, and 110, were identified by the interpretation of MS, 1H NMR, 13C NMR, HMQC, and HMBC data, and compounds 15, 20, and 126 showed high inhibitory activities on mushroom tyrosinase [31]. Ko et al. [32] reported the presence of compounds 4, 5, 133, and 134, which were isolated from the leaves of BP. In 2012, three flavans, compounds 129, 130, and 131, were isolated from the stem barks of BK and, in addition, compound 129 significantly inhibited adipocyte differentiation in 3T3-L1 cells [33]. Guo et al. [34] described the new compounds 82 and 83, together with known compound 128, which were isolated and purified from an ethyl acetate-soluble extract from the bark of BP; moreover, compounds 83 and 128 were found to strongly down-regulate the expression concentrations of estrogen receptor-α and inhibit the growth of the human breast cancer line. In the same year, compound 114 was reported for the first time by Ran et al. [35]; this compound showed definite activities against HepG-2. In 2014, the structures of compounds 11, 12, 22, 74, 78, and 127 were evaluated, on the basis of NMR spectra analysis and chemical evidence, by Yang et al. [36], and compounds 12 and 127 showed strong antioxidant activity against ABTS and DPPH. In 2018, four new flavans, compounds 116, 117, 118, and 121, as well as the known compounds 109, 122, and 123 were obtained from twigs of BK by chiral HPLC resolution; compounds 116, 117, and 118 showed the in vitro inhibition of PTP1B [37]. In 2019, compounds 108, 111, and 112 were reported by Li et al. [38]. A new isoprenylated flavonol, compound 103, and the known compounds 104, 105, and 106, were obtained from Broussonetia for the first time, being isolated from the twigs of BP; compounds 103–107 showed significant inhibitory effects on PTP1B [39]. In 2019, the metabolite investigation of root bark extracts of BP was reported by Ryu et al. [40]. The results showed that the novel compounds 98 and 99 exhibited anti-inflammatory activity by inhibiting NO production in LPS-induced RAW264.7 cells. Four new compounds (89–92) and four known compounds (93–96) were isolated from the root bark of BP [41]. Compound 91 showed inhibitory activity against tyrosinase, while compound 92 exhibited cytotoxic activity against three cancer cell lines (NCIH1975, HepG2, and MCF-7), and compound 89 inhibited the production of IL-2 in Jurkat cells [41]. In 2020, the structures of several compounds (43, 84–88) were elucidated, based on NMR and HRMS data, showing that compounds 43 and 86 could be used for inflammatory diseases [42]. Compounds 53, 54, 55, 57, 62, 64, 65, 66, 67, 68, 72, 77, 79, 80 and 81 were reported by Qureshi et al. [43]. In 2021, six previously undescribed prenylated flavonoids, compounds 32, 33, 34, 36, 39, and 42, and three known compounds, 35, 41, and 44, were isolated from the roots of BK; compounds 32, 33, and 36 showed strong dose-dependent antiosteoclastogenic activities [44]. Compounds 28–31 were isolated from the roots of BK; compounds 29 and 31 showed anti-inflammatory by inhibiting LPS–induced NO production [14]. In addition, Yadav et al. [45] reported compounds 1, 3, 6, 7, 8, 13, 17, 19, 21, 23, 24, and 25.

All flavonoids are summarized in Table 1, and the structures were summarized in Figure S1.

2.2. Penylpropanoids

Compounds with one or several C6-C3 units are classified as penylpropanoids. Several penylpropanoids, such as compound 145 and compound 150, showed anti-tumor and antioxidant activities, respectively.

A total of 50 penylpropanoids have been isolated from Broussonetia. In 2009, nine new lignans, compounds 154, 155, 172–177, and 184, and three known lignans, compounds 179, 182, and 183, were isolated from the fruits of BP; these compounds exhibited antioxidant activities against H₂O₂-induced impairment in PC12 cells [53]. In 2010, Zhou et al. [54] reported that compounds 151, 170, 171, 180, 181, and 194 were isolated from BP for the first time; these compounds showed antioxidant activity against H₂O₂-induced injury in SY5Y cells. In 2014, four compounds (148, 165, 166, and 178) were isolated from an n-butanol extract of BP, and the structures of these compounds were elucidated on the basis of NMR spectra analysis and chemical evidence [36]. In 2019, Li et al. [38] reported compounds 185–192. In 2020, compounds 162 and 167 were isolated from the CHCl3-soluble part of an ethanolic extract of branches and twigs of BP by Malanik et al. [42]. In 2021, Vu et al. [14,44] isolated compounds 156–161 from the roots of BK. In addition, compounds 145, 146, 147, 152, and 153 were reported by Yadav et al. [45].

All penylpropanoids are summarized in Table 2, and the structures were summarized in Figure S2.

2.3. Polyphenols

Compounds with two or more hydroxyl groups that are not flavonoids, phenylpropanoids, terpenes, or alkaloids are classified as polyphenols. The pharmacological effects of polyphenols, apart from skin whitening and anti-wrinkle properties, have been evaluated by researchers, but this is far from the level of research into flavonoids.

In total, 38 polyphenols were isolated from Broussonetia. In 1999, compounds 203 and 226 were isolated from the root bark of BK, and the cytotoxic activity of these compounds was evaluated against several different cell lines [27]. In 2001, Lee et al. [28] reported that compounds 195, 198, 199, 205, 206, 223, and 232 were isolated from the ethyl acetate-soluble extract of the whole plants of BP, and compound 199 exhibited to be active as aromatase inhibitors. In 2009, compounds 204, 207, 224, 225, and 231 were isolated from the methanol extract of BK, and the monophenolase inhibition of compounds 204, 224, and 225 was determined [55]. In 2018, new polyphenols, compounds 221 and 222, and known compounds 196 and 210 were isolated from the twigs of BK; compounds 196 and 222 showed the in vitro inhibition of protein tyrosine phosphatase 1B [37]. In 2019, compounds 219 and 220 were reported by Li et al. [38]. In addition, the structures of compounds 216–218 were elucidated on the basis of spectroscopic data (1D and 2D NMR, MS, MS/MS, and HRMS), and compound 218 exhibited significant inhibitory effects on the NO, iNOS, and pro-inflammatory cytokine production [40]. In 2020, compounds 208, 209, 211, 212, 123, 214, and 215 were reported by Qureshi et al. [43]. In 2021, compounds 197, 200, 201, and 202 were reported by Yadav et al. [45].

All polyphenols are summarized in Table 3, and the structures were summarized in Figure S3.

2.4. Alkaloids

Nitrogen-containing organic compounds are classified as alkaloids. Until now, there has been little research on the pharmacological effects of alkaloids.

To date, 35 alkaloids have been isolated from Broussonetia. In 1997, Shibano et al. isolated eight new pyrrolidine alkaloids, compounds 253–260, from the branches of BK; these compounds demonstrated inhibitory activity on β–galactosidase and β–mannosidase [58,59]. In 1998, the author also isolated four new pyrrolidine piperidine alkaloids, compounds 261–264, from the branches of BK [60,61]. In 1999, three new pyrrolizidine alkaloids, compounds 265–267, were also isolated from the branches of BK; these compounds showed the inhibitory activity of glycosidase [62,63]. In 2000, four new pyrrolidine alkaloids, compounds 249–252, showing the ability to inhibit glycosidase were isolated from the branches of BK [64]. In 2001, Tsukamoto et al. [65] isolated four new pyrrolidine alkaloids, compounds 244, 245, 246, and 248, and a new pyrroline alkaloid, compound 247, from the branches of BK [65]. In 2014, two isoquinonline alkaloids, compounds 241 and 242, were isolated and characterized from the fruits of BP; they showed cytotoxic activities on the BEL-7402 and Hela cell lines [66]. In 2020, compounds 238–241 were reported by Qureshi et al. [43]. In 2021, compounds 233–237 were reported by Yadav et al. [45].

All alkaloids are summarized in Table 4, and the structures were summarized in Figure S4.

2.5. Terpenoids and Steroids

Olefins where the molecular formula is an integer multiple of isoprene are classified as terpenoids. Most of the terpenoids are triterpenes.

Until now, a total of 17 triterpenes have been isolated from Broussonetia. Fang et al. reported that two known terpenoids, compounds 283 and 284, were isolated and characterized from BP in 1994 [24] and 1995 [25] respectively. In 2008, three new ent-kaurane type diterpenes, compounds 279–281, were isolated from leaves of BP; these compounds showed mild inhibition of tyrosinase and significant inhibition of xanthine oxidase [32]. In 2011, four new euphane triterpenes, compounds 274–277, were isolated from the bark of BP, and the structures of these compounds were determined by spectroscopic evidence and chemical methods [69]. In addition, compound 270 was a new tirucallane triterpenoid, and compounds 271–273 were isolated from BP for the first time. In 2019, compounds 268 and 269 were reported by Li et al. [38].

All the terpenoids are summarized in Table 5, and the structures were summarized in Figure S5.

All steroids were isolated only from BP. Three compounds (287–289) were reported by Qureshi et al. [43] in 2020, while compounds 285–286 were reported by Yadav et al. [45]. All steroids are summarized in Table 6, and the structures were summarized in Figure S6.

2.6. Other Compounds

Apart from the compounds mentioned above, a total of 49 other compounds isolated from Broussonetia species are classified as “others”.

Fang et al. [24,25] showed that compounds 329–332 were isolated and characterized from the root bark of BP. In 2007, two new megastigmane O-glucopyranosides, compounds 327 and 328, were isolated from the leaves of BP; the structures of these compounds were established by chemical methods and spectroscopic techniques, including 2D NMR [72]. In 2010, Zhou et al. [54] established that compounds 323–326, isolated from the fruits of BP for the first time, showed antioxidant activity against H₂O₂-induced injury in SY5Y cells. In 2011, a novel compound, 322, and a known compound, 321 were isolated from the n-BuOH extract of BP seeds, while their cAMP-regulating activity was evaluated by Mei et al. [73]. In 2014, compounds 316–320 were isolated from the n-butanol extract of BP, and compounds 317, 318, and 320 were found to potently inhibit estrogen biosynthesis in KGN cells [36]. Moreover, compounds 309–314 were reported by Yu et al. [51]. In 2016, compounds 333–338 were isolated from the ethyl acetate leaf extract of BL [71]. In 2019, compounds 293–308 were reported by Li et al. [38]. In 2021, compounds 290 and 291 were reported by Yadav et al. [45].

All these compounds were summarized in Table 7, and the structures were summarized in Figure S7.

3. Pharmacology

Various uses of Broussonetia species have inspired researchers’ interest in exploring pharmacological activities by scientific pharmacological assays including in vitro and in vivo. A variety of crude extracts and purified compounds from Broussonetia species have been evaluated for different biological effects, such as their antitumor, antioxidant, anti-inflammation, antidiabetic, anti-obesity, antibacterial, and antiviral properties, as well as skin whitening, anti-wrinkle, and other activities. Despite the extensive bioactivities that have been identified, the targeted clinical trials that are normally used to evaluate safety and effectiveness for humans are currently absent. Perhaps the addition of clinical trials might be a more comprehensive and scientific way to ascertain the medical role of the Broussonetia genus. All these pharmacological activities are summarized in Table 8.

3.1. Anti-Tumor

In 2010, the dichloromethane fraction extracted from the stem barks of BP was found to induce apoptosis-related DNA fragmentation; it increased sub-G1 accumulation, increased p53, caspase3, and Bax expression, and inhibited the proliferation of human colon cancer HT-29 cells [74]. The ethanol extract of BP exhibited the inhibition of the growth of human osteosarcoma MG63 cells, affected morphological apoptosis, and induced cell-cycle arrest, as found in 2013 [75]. In 2014, seven alkaloids isolated from the ethyl acetate fraction of BP fruits at dosages of 1, 5, 10, and 50 mg/mL showed high cytotoxic activities on the BEL-7402 and Hela cell lines, with IC₅₀ values of 6.61–47.41 mg/mL and 5.97–40.17 mg/mL, respectively [66]. Zhu et al. [76] explored the mechanism of gastric carcinoma cell SGC-7901 apoptosis, as induced by CALCBP, and the results showed that apoptosis might be related to oxidative stress in the cell mitochondria via the p38-MAPK and ERK-MAPK signal pathways. In an in vitro assay, polyphenols showed significant apoptotic activities on HepG2 cells in a dose-dependent and time-dependent manner by inducing cell cycle arrest at the G1 phase, unregulating the ratio of Bax/Bcl-2 and inhibiting the expression of PKB/AKT and ERK [77].

In 1999, the pure compounds kazinol Q, kazinol R, kazinol D, kazinol K, and 7,4′-dihydroxyflavan, isolated from BP root barks, showed strong inhibitory effects on T24, CaSki, PLC/PRF/5, HT3, and SiHa, respectively [27]. In 2011, Wei et al. explored the ability of kazinol Q to induce DNA breakage in the presence of Cu; the results showed that the cell viability of gastric carcinoma SCM-1 cells was significantly decreased [78]. In 2013, (+)-pinoresinol-4′-O-β-D-glucopyranosyl-4″-O-β-D-apiofuranoside, apigenin-6-C-β-D-glucopyranside, and liriodendrin, isolated and purified from BP leaves, exhibited inhibitory effects on HepG-2 cells during the dosage of 100 mmol·L−1; their IC₅₀ values were 17.19, 14.56, and 19.53 μg/mL, respectively [35]. Moreover, broussoflavonol B restricted the growth of breast cancer SK-BR-3 cells and breast cancer MDA-MB-231 cells at sub-micromolar concentrations via inducing cell-cycle arrest at the G0/G1 and G2/M phases and inducing the differentiation of cells [79]. In the same year, broussoflavonol B and 5,7,3′,4′-tetrahydroxy-3-methoxy-8,5′-diprenylflavone were prepared from an ethyl acetate-soluble fraction of BP barks, exerting potent antiproliferation activities on the ER-positive MCF-7 cells, with IC₅₀ values of 4.41 and 4.19 mM, respectively [34]. The two compounds could also inhibit tumor proliferation on BCAP-37 cells in vivo, from a dosage of 0–25 µM [34]. In 2016, kazinol A showed cytotoxicity in T24 and T24R2 cells from a dosage of 0–50 µM via G0/1 arrest, mediated by decreasing cyclin D1 and increasing p21 [80]. In addition, kazinol E was a targeted molecule for breast cancer stem-like cells from a dosage of 0–50 µM, by blocking EGF-induced ERK activity directly [81,82]. Moreover, in 2017, Kim et al. identified that marmesin eliminated mitogen-stimulated proliferation and invasion in both p53 wild-type A549 and p53-deficient H1299 NSCLC cells [83]. In 2018, Park et al. reported that broussochalcone A showed high cytotoxic activities in human hepatoma HepG2 and SK-Hep1 cells, with an IC₅₀ value of 20 µM from a dosage of 0–40 µM; these activities were due to cell-cycle arrest by increasing FOXO3, regulating the cell cycle, and activating pro-apoptotic proteins [84]. In another study conducted by Shin et al. in 2019, broussochalcone A also exerted strong cytotoxic effects upon colon and liver cancer cells with a dosage of 0–20 μM, by promoting the phosphorylation/ubiquitin-dependent degradation of β-catenin [85]. In 2019, broussoflavonol K showed stronger inhibitory effects on NCI-H1975, MCF-7, and HepG2 than isolicofavonol, with IC₅₀ values ranging from 0.90 to 2.00 μM, which were due to cyclization between the isoprenyl moiety and the adjacent phenolic hydroxyl group [41]. A recent study in 2020 investigated the anti-tumor effect of broussoflavonol B; the results showed that it significantly repressed the proliferation of human pancreatic cancer PANC-1 cells, by inactivating the ERK/c-Myc/FoxM1 signaling pathway, with a dosage of 0–100 μM [86]. In 2021, Vu et al. studied the inhibitory effects of eriodictyol, apigenin, and kaempferol against HL-60 cells, with IC₅₀ values ranging from 46.43 to 94.06 μM [14]. In a study in 2022, marmesin also exerted cytotoxicity on esophagus cancer cells via inhibiting the PI3K/Akt pathway [87]. From this evidence, it is clear that AMPK is a major regulator of energy metabolic pathways and plays an important role in the regulation of autophagy. In this work, the active compound kazinol C, isolated from BK whole herbs or root barks, could markedly induce apoptosis in colon cancer cells by activating AMPK phosphorylation [2,88].

3.2. Anti-Oxidant Activity

Excessive oxidative stress is harmful to cells, protein, DNA, and others, so antioxidants are important molecules that can protect humans from this danger. Various assays of antioxidant activity have been used to test these properties, such as DPPH, ABTS, CAA, hydrogen peroxide scavenging activity assays, hydroxyl radical scavenging activity assays, FRAP, lipid peroxidation inhibitory activity, mitochondrial swelling assays, chelation of metal ions (Fe²⁺) assays, xanthin oxidase inhibitory activity assays, hydroxyl radical scavenging activity, superoxide anion free radical scavenging activities, superoxide anion radical scavenging activity assays, ferrous ion chelating capacity assays, and TEAC.

The antioxidant activities of the crude extracts of Broussonetia species were measured via the methods mentioned above, of which the most frequently used methods were DPPH, ABTS, FRAP, and hydroxyl radical scavenging activity assays. In 2014, DPPH and pyrogallol autoxidation assays showed that the hydroxyl radical inhibition rate of the seed oil of BP was 91.21% [89]. In the same year, the ethanol extract of BP fruits was revealed to demonstrate antioxidant activity (0–400 mg/mL), with an IC₅₀ value of 155.7 µg/mL for lipid peroxidation inhibition on liver homogenate [90]. In 2013, the ethanolic extract of BP fruits showed maximum antioxidant activity by DPPH assay during the dose of 0–600 µg/mL, with an IC₅₀ value of 156.3 µg/mL [75]. In 2012, Sun et al. indicated that the ethanol extract from BP flowers showed more potent radical scavenging activity than the water extract, which showed 62.88% in the DPPH assay at 5 mg/mL and 61.15% in terms of chelation Fe²⁺-activity at 6 mg/mL [91]. In another experiment, Sun et al. reported that the ethanol and water extracts of BP fruits showed strong DPPH radical-scavenging activity at 87.17 ± 0.18% and 58.11 ± 0.11%, respectively [7,91]. The Fe²⁺-chelating activity was approximately 77.51% and 48.26% from an aqueous extract of 5 mg/mL and an ethanol extract of 5 mg/mL [7,91].

Several pure compounds of Broussonetia species also showed antioxidant effects in vitro, apart from the extracts mentioned above. In 2020, broussoflavonol A, 5,7,3′,4′-tetrahydroxy-3-methoxy-8,5′-diprenylflavone and kazinol M isolated from BP branches and twigs have shown good antioxidant activities, with CAA values of 25.9, 6.4, and 5.4, respectively [42]. In 2014, luteolin, luteoloside, orientin, and isoorientin showed strong radical scavenging activities by DPPH from a dosage of 0.1–3 mg/mL, with SC50 values of 19.72, 19.67, 18.86, and 19.33 mmol/L, respectively [36]. In 2012, Ryu et al. indicated that broussochalcone A and 3,4-dihydroxyisolonchocarpin, isolated from BP roots, showed the highest antioxidant activities within a dosage of 0.1–1000 µM, with IC₅₀ values of 27.6 ± 0.3 µM and 21.8 ± 0.2 µM through DPPH and IC₅₀ values of 5.8 ± 0.1 µM and 7.7 ± 0.4 µM through ABTS, as well as IC₅₀ values of 0.6 ± 0.04 µM and 1.8 ± 0.1 µM through an XOD assay [57]. In 2010, curculigoside C, ferulic acid, dihydroconiferyl alcohol, and 3,4-dihydroxybenzoic acid were revealed to have antioxidant activities within a dose of 0.16 to 100 mM, with the IC₅₀ values of 39.5, 58.9, 65.3, and 65.6 mM, respectively [54]. In 2009, MTT and DPPH assays showed that erythro-1-(4-hydroxy-3-methoxyphenyl)-2-{4-[(E)3-hydroxy-1-propenyl]-2-methoxyphenoxy}-1,3-propanediol, isolated from BP fruits (0.16–100 µM), possessed significant antioxidant activities with an IC₅₀ value of 60.9 µM [53]. In a diphenyl-2-picrylhydrazyl assay system, broussochalcone A exerted stronger radical scavenging activity within a dose of 1–30 µM than α-tocopherol at IC0.200 values of 7.6 ± 0.8 µM [92]. Broussoflavonol F, broussoflavan A, broussoaurone A, and broussoflavonol G inhibited the Fe²⁺-induced formation of TBARS in a concentration-dependent manner, with IC₅₀ values of 2.1, 2.7, 1.0 and 1.2 µM, respectively [46].

From Table 8, it can be seen that a plethora of investigations revealed that the roots and leaves possessed stronger antioxidant activities than other parts [93]. Moreover, many assays indicated that the antioxidant activities of bark extracts were superior to wood extracts [94].

3.3. Anti-Inflammation

In 2001, broussochalcone A, isolated from BP at a dose of 1–20 μM could inhibit NO production in LPS-activated macrophages by inhibiting IkBa phosphorylation, IkBa degradation, nuclear factor-kappa B activation, and iNOS expression, with an IC₅₀ value of 11.3 mM [92]. In 2003, papyriflavonol A, isolated from BP, was demonstrated to inhibit human group IIA and V sPLA2s dose-dependently and reduce IgE-dependent passive cutaneous anaphylaxis in rats from a dose of 0–250 μM with IC₅₀ values of 3.9 to 4.5 mM, suggesting that it could be a novel anti-inflammatory drug in the future [95]. In 2019, Huang et al. demonstrated that broussonin E, isolated from the bark of BK, could treat inflammatory diseases by modulating the activation state of macrophages by suppressing ERK and p38 MAPK and enhancing the JAK2-STAT3 signaling pathway [96]. In the same year, flavanone, broussochalcone C, broussoflavanonol A, kazinol V, kazinol W and broussoflavonol B, isolated from root bark in 100% methanol, were shown to have potent anti-inflammatory effects on LPS-stimulated RAW264.7 cell through downregulating iNOS, COX-2, and TNF-α expression within the dose of 1.25–40 μM [40]. In the same year, the anti-inflammatory effect of broussoflavonol H was studied by Tian et al.; the results showed that the compound could significantly suppress the production of IL-2 in Jurkat induced by PHA and PMA, with an IC₅₀ value of 9.95 μM [41]. Moreover, in 2020, 5,7,3′,4′-tetrahydroxy-3-methoxy-8,5′-diprenylflavone, kazinol M, broussoflavonol B, broussoflavonol A, and broussofluorenone C, isolated from the branches and twigs of BP, showed anti-inflammatory effects by activating NF-κB/AP-1 [42]. In 2021, eriodictyol, apigenin, and kaempferol reduced LPS-induced iNOS expression within the dosage of 0–30 μM in a dose-dependent manner, with IC₅₀ values of 11.98, 10.16, and 24.06 μM, respectively [14].

In 2008, the ethanol extract of BP roots was shown to reduce abdominal Evan’s blue extravasations, including serotonin and sodium nitroprusside, caused by inflammatory mediators; the effects might be related to inhibiting the vascular permeability via autocrines and NO [97]. In 2010, the anti-inflammatory effect of methanol extract of BP heartwood was investigated in NC/Nga mice induced by an extract of the house-dust mite, Dermatophagoides farina; the results showed that the methanol extract could obviously inhibit AD-like skin lesions by decreasing the levels of IgE and IL-4 and inhibiting the induction of TARC/CCL17, MDC/CCL22, and RANTES/CCL5 in HaCaT cells [98]. Furthermore, it was reported that the n-hexane fraction and n-butanol fraction of the methanol extract of BP stem bark at a dosage of 10–80 μg/mL were found to have significant anti-inflammatory activities in RAW 264.7 cells by inhibiting NO and pro-inflammatory cytokine production [74,97]. In 2014, the ethanol extract of BK leaves within a dose of 200–1000 μg/mL could treat Nc/Nga mice that were predisposed to develop AD-like skin lesions induced by D. farinae extract; further study demonstrated that its mechanism might be related to significantly downregulating the plasma levels of IgE and IL-4, as well as inhibiting hTARC secretion in HaCaT cells by activated TNF-α/IFN-γ [97].

In general, the anti-inflammatory activity of Broussonetia species was mainly studied in a murine macrophage RAW264.7 cell model and in mice stimulated with LPS. Moreover, the mechanism of anti-inflammatory activity was mainly concentrated on inhibiting NO production and iNOS expression. iNOS was primarily found in macrophages induced by LPS or cytokines to produce a high level of NO as a pro-inflammatory mediator [49]; therefore, the inhibition of NO production or iNOS expression was a critical strategy for the treatment of inflammatory diseases.

3.4. Anti-Diabetic and Anti-Obesity Effects

Diabetes is a chronic disease that presents as high levels of glucose in the blood, which may be caused by insulin deficiency and insulin resistance. All in vitro and in vivo studies have demonstrated the antidiabetic effects of different extracts and compounds prepared from Broussonetia species.

In 2008, Cha et al. indicated that the ingestion of stem bark powder from BK decreased the serum levels of glucose, fructosamine, triglyceride, and total cholesterol, as well as the activity of ALT in the genetically diabetic OLETF rats; the important regulatory factor would be the increased blood insulin level in the animal model [16]. In 2010, Ryu et al. showed that broussochalcone A, papyriflavonol A, broussochalcone B, kazinol A, kazinol B, and 8-(1,1-dimethylallyl)-5′-(3-methylbut-2-enyl)-3′,4′,5,7-tetrahydroxyflanvonol have inhibitory effects against α-glucosidase with a dose of 0.01–1000 μM; the IC₅₀ values were 5.3, 11.1, 12.0, 26.3, 3.6, and 2.1 μM, respectively [56]. Moreover, kazinol U [99], isokazinol D, and kazinol C [100] showed therapeutic potential in delaying pancreatic β-cell destruction in type 1 diabetes by blocking the NF-kB pathway in pancreatic β-cells and reducing RINm5F cell damage. A report in 2012 indicated the anti-obesity effect of broussonone A, as well as of other isolated phenolic compounds isolated from BK stem barks, the mechanism being related to noncompetitive inhibitory activity on pancreatic lipase, with an IC₅₀ of 28.4 µM and an inhibitory effect of adipocyte differentiation in 3T3-L1 cells [33]. In 2016, antidiabetic activity was also observed in mouse 3T3-L1 preadipocyte cells and C2C12 myoblast cells. Lee et al. demonstrated that kazinol B, isolated from BK roots, within a dose of 0–20 μM could increase insulin sensitivity via improving glucose uptake through the insulin-Akt signaling pathway, along with AMPK activation [101]. In 2020, treatment with broussoflavonol B and kazinol J in HFD-fed C57BL6 male mice within the dosage of 0–100 μg/mL, showed therapeutic potential in obesity and type 2 diabetes via suppressing pro-inflammatory responses by activating AMPK in 3T3-L1 adipocytes [102]. In addition, an ethanolic extract of BK fruits could treat β-cell damage by preventing STZ-induced oxidative stress and suppressing β-cell apoptosis via inhibiting Erk phosphorylation, as found in mice injected with STZ [15], and it could also treat diabetic nephropathy via the activation of Nrf2 and provide protection against PA-induced lipotoxicity in the mesangial cells in diabetes [103].

In a word, the mechanism of anti-diabetic effects is mainly related to blocking the NF-kB pathway and inhibiting α-glucosidase activity. The generation of NO via iNOS and reactive oxygen species plays an important role in pancreatic β-cell damage. The NF-kB transcription factor was activated by oxidative stress due to reactive oxygen species as well as regulating iNOS expression. Thus, the NF-kB pathway can protect the β-cell from damage [99].

3.5. Antibacterial and Antiviral Effects

Some studies have shown that the extracts or pure compounds of Broussonetia species could suppress bacteria. In 2015, N. Naveen Kumar et al. [104] reported that the hexane extract of BP seeds showed high inhibitory activity on Staphylococcus aureus, Proteus vulgaris, Bacillus cereus, and Enterobacter aerogenes, whereas it had no inhibitory effect on fungal strains [104]. In 2017, Park et al. analyzed the antibacterial activity of papyriflavonol A within the dosage of 1–1000 µM; the results showed that the potent inhibitory effect of PLpro, with an IC₅₀ value of 3.7 μM, along with a further study, showed that it may be a potential anti-COVID-19 agent [105]. Geng et al. [17] indicated that 5,7,3′,4′-tetrahydroxy-3-methoxy-8,5′-diprenylflavone, isolated from the BP air-dried aerial part, showed more antibacterial activity in suppressing Actinomyces naeslundii and Porphyromonas gingivalis (MIC = 1.95 ppm) than the positive control, triclosan, at a dosage of 0.12–250 ppm. In 2021, Ghosh et al. [18] found that six polyphenols (broussochalcone A, papyriflavonol A, 3′-(3-methylbut-2-enyl-3′,4′,7-trihydroxyflavane, broussoflavan A, kazinol F, and kazinol J) showed greater Mpro inhibitory effect than two repurposed drugs (lopinavir and darunavir) and may serve as promising anti-COVID-19 drugs.

3.6. Skin Whitening and Anti-Wrinkle Activities

In 2019, Lim et al. [19] reported that kazinol U, a constituent of BK root barks, could attenuate melanogenesis within a dose of 0–20 μM via inhibiting MITF expression, inactivating target genes such as tyrosinase, Tyrp1, and Tyrp2, and activating AMPK and MAPK proteins in both in vitro and in vivo experiments. In the same year, it was reported that collagen is the major structural protein in the extracellular space of the connective tissue of the skin, and BK stem extract could maintain skin collagen content via inactivating the reactive oxygen species and inhibiting collagenase activity [106].

3.7. Other Properties

Out of these pharmacological activities displayed above, Broussonetia species also showed the treatment of bone diseases, liver protection, promoting hair growth, anti-angiogenic activities, anticholinesterase effects, increasing cAMP, immune-stimulating activity, and antinociceptive.

In 2021, Vu et al. observed the antiosteoclastogenic activity of broussonols F, G, and K; the results showed that the compounds significantly inhibited RANKL-induced osteoclast formation with a dosage of 10–30 μM in RAW264.7 cells and they may be the lead compounds against bone diseases in the future [44]. In 2020, CSZ extract increased liver function and alleviated DILI in rats induced in acetaminophen (APAP) via regulating the TLR3/JNK/c-jun/c-fos/JAK/STAT3 pathway [107]. In 2020, Lee et al. [108] showed that ethanolic extract of BP had the capacity of promoting hair growth by regulating β-Catenin and STAT6 target proteins in human hair follicle dermal papilla (hHFDP) cells within a dose of 0–20 µg/mL. In 2014, the ethanolic extract of BK twigs was found to have anti-angiogenic activities with a dosage of 0.1–10 µg/mL; the mechanisms were the inhibition of VEGF-A, stimulated by the phosphorylation/activation of ERK, Akt, and p70S6K, and the downregulation of VEGFR-2 and MMP-2 in human umbilical vein endothelial cells [109]. In 2012, three prenylated flavonols, 8-(1,1-dimethylallyl)-5′-(3-methylbut-2-enyl)-3′,4′,5,7-tetrahydroxyflanvonol,papyriflavonol A, and broussoflavonol B, isolated from BP roots, suppressed two human cholinesterases related to Alzheimer’s disease (AD) in a dose-dependent manner, with IC₅₀ values ranging from 0.8 to 3.1 μM and from 0.5 to 24.7 μM against HAChE and BChE, respectively [47]. In the next year, the immune-stimulating activity of mice that were immunized intraperitoneally with OVA/alum (100 μg/200 μg) was tested; the results showed that mice given BK water extract orally for 21 days could enhance the Th1 immune response and showed no cytotoxicity in the model system [110]. In 2010, Lee et al. [50] explored the estrogenic activity of broussonin A, (+)−(2R) kazinol I, tupichinol C and kazinol U, which showed that these compounds could regulate the E2-responsive genes as functional ER ligands such as E2 in the ER-sensitive MCF-7 cells at 10 µM. Kazinol P, a natural compound isolated from BK, showed the therapeutic effects of improving muscle regeneration and repair with the mechanism of promoting myogenic differentiation through activating p38MAPK and MyoD transcription activities [111]. In a study in 2003, Kazinol B, an isoprenylated flavan, showed significant inhibitory activities of nitric oxide (NO) in lipopolysaccharide-activated macrophages, with an IC₅₀ of 21.6 mM [112].

Table 8. Pharmacological effects of Broussonetia species.

	Variety	Parts	In Vivo/In Vitro	Model	Active Components	Dosage	Results	References
Anti-tumor	BK	-	in vitro	Colon cancer cells	Kazinol C	0–30 μM	Inducing apoptosis by activating AMPK.	[2]
	BK	Roots	in vitro	Hela, HL-60, MCF-7 cells	Eriodictyol, apigenin and kaempferol	-	Cytotoxic activity against HL-60 cells (IC₅₀ = 46.43–94.06 μM) and apigenin was cytotoxic against Hela cells (IC₅₀ = 49.26 μM).	[14]
	BP	Barks	in vitro	HepG2 cells	Polyphenols	0–500 μg/mL	Induced mitochondria-mediated apoptosis by inactivating ERK and AKT signaling pathways.	[77]
	BK	Stem barks	in vitro	PANC-1 cells	Broussoflavonol B	0–100 μM	Repressing proliferation by inactivating the ERK/c-Myc/FoxM1 signaling pathway.	[86]
	BP	Barks	in vitro	MDA-MB-231 cells	Broussoflavonol B	0–1 µM	Inducing the arrest of the cell cycle and cell death.	[79]
	BP	Barks	in vitro	SK-BR-3 cells	Broussoflavonol B	0–1 µM	Inhibiting growth and inducing differentiation of stemlike SK-BR-3 cells.	[113]
	BP	-	in vitro	Colon and liver cancer cells	Broussochalcone A	0–20 μM	Cytotoxicity by promoting phosphorylation/ubiquitin-dependent degradation of β-catenin.	[85]
	BP	Root barks	in vitro	NCI-H1975, HepG2 and MCF-7	Broussoflavonol K	-	IC₅₀ = 0.90–2.00 μM	[41]
	BP	Barks	in vitro	SGC-7901 cells	Chlorogenic acid-like compounds	50, 100 and 200 μg/mL	Inducing apoptosis through p38-MAPK and ERK-MAPK signaling pathways.	[76]
	BP	-	in vitro	HepG2 and SK-Hep1 cells	Broussochalcone A	0, 2.5, 5, 10, 20 and 40 µM	Cell cycle arrest by increasing FOXO3 and cell cycle regulatory and pro-apoptotic proteins (IC₅₀ = 20 µM).	[84]
	BK	-	in vitro	Esophagus cancer cells	Marmesin	-	Inhibiting the PI3K/Akt pathway.	[87]
	BK	-	in vitro	NSCLC cell	Marmesin	0–10 µM	Abrogating mitogen-stimulated proliferation and invasion.	[83]
	BP	Roots	in vitro	T24 and T24R2 cells	Kazinol A	0–50 µM	Cytotoxicity through G _0/1 arrest mediated by cyclin D1 decrease and p21 increase.	[80]
	BK	Roots	in vitro	MCF-7 cells	Kazinol E	0–50 µM	Blocking EGF-induced ERK activity.	[81]
	BK	Root barks	in vitro	MCF-7 cells	Kazinol E	-	Inhibiting Erk activity by binding the ATP-binding pocket of Erk-1.	[82]
	BK	Root barks	in vitro	HT-29 colon cells	Kazinol C	0–120 µM	Promoting AMPK phosphorylation and attenuating HT-29 colon cancer cell growth and viability.	[88]
	BP	Fruits	in vitro	A375, BEL-7402 and Hela cells	Total alkaloids and seven individual alkaloids	50, 10, 5, and 1 mg/mL	IC₅₀ = 6.61–47.41 mg/mL (BEL-7402 cell line) and IC₅₀ = 5.97–40.17 mg/mL (Hela cell line).	[66]
	BP	Leaves	in vitro	HepG-2 cells	(+)-pinoresinol-4′-O-β-D-glucopyranosyl-4″-O-β-D-apiofuranoside, liriodendrin, apigenin-6-C-β-Dglucopyranside	100 mmol/L	IC₅₀ were 17.19, 14.56 and 19.53 μg/mL respectively.	[35]
	BP	Fruits	in vitro	MG63 cells	Ethanol extract	0–7000 µg/mL	Inhibiting the proliferation associated with apoptosis and cell cycle arrest.	[75]
	BP	Barks	in vitro	MCF-7 cells	5,7,3′,4′-Tetrahydroxy-3-methoxy-8,50-diprenylflavone and broussoflavonol B	0–25 µM	Showing high anti-proliferation activities with IC₅₀ values of 4.41 and 4.19.	[34]
	BK	-	in vitro	SCM-1 cells	Kazinol Q	0–120 µM	Enhancing subsequent cell death due to necrosis.	[78]
	BP	Stem Barks	in vitro	HT-29 cells	Dichloromethane Fractions	50, 100, 150, or 200 μg/mL	Inducing apoptosis through p53-dependent mitochondrial signaling pathway.	[74]
	BK	Roots barks	in vitro: Human hepatoma,	PLC/PRF/5, T24 cells, human cervical carcinoma, HT-3, SiHa and CaSki cells	kazinols Q, and R, kazinol D, K, H, 7,4′-dihydroxyflavan	-	Showing the great inhibitory effect to T24, CaSki, PLC/PRF/5, HT3 and SiHa respectively.	[27]
Anti-oxidant activity	BP	Barks	in vitro	-	Ethanol extracts	-	IC₅₀ value was 0.33 ± 0.08 mg/mL	[13]
	BP	Branches and twigs	in vitro	THP-1 cells	5,7,3′,4′-tetrahydroxy-3-methoxy-8,5′-diprenylflavone, kazinol M,broussoflavonol A	-	CAA values were 25.9, 6.4, 5.4 respectively.	[42]
	BP	Whole plants	in vitro	-	Lignin	10–100 mg/L	Lignin with more phenolic hydroxyl groups.	[114]
	BP	Fruits	in vitro	-	Three purified fractions	0–2.0 mg/mL	IC₅₀ values of three purified fractions were 0.54, 0.86, and 0.57 mg/mL respectively.	[115]
	BP	Leaves	in vitro	KGN cells	Luteolin, luteoloside, orientin, isoorientin	0.1–3 mg/mL	SC₅₀ values was 19.72, 19.67, 18.86 and 19.33 mmol/L respectively.	[36]
	BP	Seeds	in vitro	-	Seed oil	0.2–0.8 v/v	The hydroxyl radical inhibition rate was 91.21%	[89]
	BP	Fruits	in vitro	-	Ethanol extract	0–400 mg/mL	IC₅₀ for lipid peroxidation inhibition on liver homogenate was 155.7 µg/mL	[90]
	BP	Fruits	in vitro	MG63 cells	Ethanolic extract	0–600 µg/mL	DPPH assay showed IC₅₀ value of 156.3 µg/mL.	[75]
	BP	Flowers	in vitro	-	Ethanol and water crude extracts	5 mg/mL 6 mg/mL	The ethanol extract showing 62.88% in the DPPH radical scavenging method and 61.15% in chelation Fe²⁺-activity.	[91]
	BP	Fruits	in vitro	-	Ethanol and water crude extracts	DPPH: 0.5–5 mg/mL Fe²⁺-activity: 0.5–5 mg/mL	DPPH radicals with a percentage inhibition of 87.17 ± 0.18% to ethanol extract and 58.11 ± 0.11% to aqueous extract.Fe²⁺-chelating activity of approximately 77.51% of aqueous extract and the ethanol extract showed a chelation capacity of 48.26%.	[7]
	BP	Roots	in vitro	-	Broussochalcone A and 3,4-dihydroxyisolonchocarpin	0.1–1000 µM	IC₅₀ values of 27.6 ± 0.3 µM and 21.8 ± 0.2 µM through DPPH assay, which IC₅₀ values of ABTS were 5.8 ± 0.1 µM and 7.7 ± 0.4 µM as well as IC₅₀ values of XOD were 0.6 ± 0.04 µM and 1.8 ± 0.1 µM.	[57]
	BP	Fruits	in vitro	RAW264.7 cells	Petroleum extract	DPPH: 0.31 to 5.0 mg/mL superoxide anion radical scavenging activity: 2.5–40 mg/mL hydroxyl radical scavenging activity: 0.625–10 mg/mL	IC₅₀ = 8.20 ± 0.003 mg/mL (DPPH). IC₅₀= 89.86 ± 3.40 mg/mL (superoxide anion). IC₅₀ =19.63 ± 0.36 mg/mL (hydrogen peroxide).	[116]
	BP	Fruits	in vitro	SY5Y cells	3,4-dihydroxybenzoic acid, dihydroconiferyl alcohol, ferulic acid and curculigoside C	0.16–100 mM	The IC₅₀ values were 39.5, 58.9, 65.3, and 65.6 mM respectively through a DPPH assay.	[54]
	BP	Barks and woods	in vitro	-	Ethyl acetate fractionhexane fraction	-	The antioxidant activity of bark extract was superior to that of wood.	[94]
	BP	Radixes and leaves	in vitro	SH-SY5Y cells	Methanol extract	0.1–2.5 mg/mL	BP radixes and leaves possessed the best scavenging activities for DPPH, ABTS radical, and H₂O₂.	[93]
	BP	Fruits	in vitro	PC12 cells	Erythro-1-(4-hydroxy-3-methoxyphenyl)-2-{4-[(E)3-hydroxy-1-propenyl]-2-methoxyphenoxy}-1,3-propanediol	0.16–100 µM	IC₅₀ =60.9 µM (DPPH assay).	[53]
	BP	-	in vitro	RAW 264.7 cells	Broussochalcone A	1–30 µM	IC₀.₂₀₀ was 7.6 ± 0.8 µM (diphenyl-2-picrylhydrazyl assay system).	[92]
	BP	Roots	in vitro	-	Broussoflavan A, broussoflavonol F,broussoflavonol G, broussoaurone A	-	Inhibiting the Fe²⁺-induced formation of TBARS with IC₅₀ values of 2.1, 2.7, 1.0 and 1.2µM respectively.	[46]
Anti-inflammation	BK	Roots	in vitro	RAW264.7 cells	Eriodictyol, apigenin, kaempferol	0–30 μM	Reducing iNOS expression with IC₅₀ values of 11.98, 10.16, and 24.06 μM.	[14]
	BP	Branches and twigs	in vitro	THP-1 cells	Kazinol M, broussoflavonol B, broussoflavonol A, 5,7,3′,4′-tetrahydroxy-3-methoxy-8,5′-diprenylflavone and broussofluorenone C	1 μM	Activating NF-κB/AP-1.	[42]
	BP	Root barks	in vitro	NCIH1975, HepG2, and MCF-7 cells	Broussoflavonol H.	-	Inhibiting the production of IL-2 in Jurkat induced by PHA and PMA (IC₅₀ = 9.95 μM).	[41]
	BP	Root barks	in vitro	RAW264.7 cells	Flavanone, broussochalcone C, broussoflavanonol A, kazinol V, kazinol W and broussoflavonol B	1.25–40 μM	Reducing NO production through downregulating iNOS, COX-2, and TNF-α expression and the expression of iNOS protein.	[40]
	BK	Barks	in vitro	RAW264.7 cells	Broussonin E	2.5–20 μM	Inhibiting the ERK and p38 MAPK and enhancing the JAK2-STAT3 signaling pathway.	[96]
	BK	Leaves	in vivo	mice	Ethanol extract	200–1000 μg/mL	Down-regulating the plasma levels of IgE and IL-4 and inhibiting hTARC secretion in HaCaT cells by activated TNF-α/IFN-γ.	[117]
	BP	Stem barks	in vitro	RAW 264.7 cells	n-hexane fractionof methanol extract	10–80 μg/mL	Inhibiting the NO production and proinflammatory cytokines.	[118]
	BP	Stem barks	in vitro	RAW 264.7 cells	n-butanol fraction	0–150 μg/mL	Inhibiting iNOS expression in RAW 264.7 macrophages.	[74]
	BK	Heartwood	in vivo	mice	EtOH extract	50–250 mg/mL	Inhibiting IgE production in β-cell and mast cell infiltration by IL-4 and chemokines by inhibiting Th2-cell activation by allergens.	[98]
	BP	-	in vivo	-	Ethanol extract	-	Inhibiting vascular permeability via autocrines and nitric oxide.	[97]
	BP	-	in vitro	Bone marrow cells	Papyriflavonol A	0–250 μM	Inhibiting human group IIA and V sPLA2s with IC₅₀ values of 3.9 and 4.5 mM.	[95]
	BP	-	in vitro	RAW 264.7 cells	Broussochalcone A	1–20 μM	Inhibiting NO production with an IC₅₀ of 11.3 mM via inhibition of IkBa phosphorylation, IkBa degradation, nuclear factor-kappa B activation, and iNOS expression.	[92]
	BK	Root barks	in vitro	RAW 264.7 cells	Tupichinol C, kazinol U, kazinol A, kazinol I, broussonin A, kazinol C, kazinol D	0–20µM	Suppressing the LPS-induced high level of NO with IC₅₀ values of less than 6 µM and attenuating protein and mRNA levels of inducible iNOS.	[49]
Anti-diabetic and Anti-obesity Effects	BK	Fruits	in vivo	mice	Ethanolic extract	-	Inhibiting Erk phosphorylation by preventing STZ-induced oxidative stress and beta cell apoptosis.	[15]
	BK	Fruits	in vitro	SV40 MES13 cells	Ethanolic extract	0–40 μg/mL	Ethanolic extract induced the expression of antioxidant enzymes by activating Nrf2 and prevented palmitate-induced lipotoxicity.	[103]
	BP	Root barks	in vivo	mice	Broussoflavonol B and kazinol J	0–100 μg/mL	Suppressing pro-inflammatory responses via activating AMPK.	[102]
	BK	Root barks	in vivo	mice	Kazinol C and isokazinol D	5–25 μM	Blocking the NF-κB pathway and reducing the extent of β-cell damage.	[100]
	BK	Stem barks	in vitro	3T3-L1 cells	Broussonone A together with other isolated phenolic compounds	100 µM	Inhibitory activity against pancreatic lipase with IC₅₀ of 28.4 µM, and has inhibitory effects on adipocyte differentiation.	[33]
	BK	Root barks	in vitro	RINm5F cells	Kazinol U	0–60 μM	Blocking the NF-kB pathway and reducing cells damage.	[99]
	BP	Roots	-	-	Broussochalcone A, broussochalcone B, kazinol A, kazinol B, 8-(1,1-Dimethylallyl)-5′-(3-methylbut-2-enyl)-3′,4′,5,7-tetrahydroxyflanvonol and papyriflavonol A	0.01–1000 μM	IC₅₀ values of 5.3, 11.1, 12.0, 26.3, 3.6, and 2.1μM respectively.	[56]
	BK	Stem barks	in vivo	mice	Stem bark powders	-	Decreasing the serum levels of glucose, fructosamine, triglyceride, and total cholesterol and the activity of ALT, and increasing blood insulin level.	[16]
Antibacterial and Antiviral Effects	BP	-	in vitro	-	Broussochalcone A, papyriflavonol A,3′-(3-methylbut-2-enyl)-3′,4′,7-trihydroxyflavane, broussoflavan A, kazinol F and kazinol J	-	These six polyphenols are more potent Mpro inhibitors than two repurposed drugs (lopinavir and darunavir).	[18]
	BP	Whole plants	in vitro	-	5,7,3′,4′-tetrahydroxy-3-methoxy-8,5′-diprenylflavone	0.12–250 ppm	Suppressing Porphyromonas gingivalis (MIC = 1.95 ppm).	[17]
	BP	Roots	in vitro	-	Papyriflavonol A	1–1000 µM	Inhibitory effect of PLpro with an IC₅₀ value of 3.7 µM.	[105]
	BP	Fruits	in vitro	-	BPP-3	0.4–2.0 mg/mL	The minimum inhibitory concentration of BPP-3 against E. coli, P. aeruginosa, B. subtilis and S. aureus were 0.3 mg/mL, 0.25 mg/mL, 0.3 mg/mL and 0.25 mg/mL, respectively.	[115]
	BP	Seeds	in vitro	-	Hexane extract	0.25%, 0.5%, 1%, 2%, and 4% (v/v)	The seed oil has an inhibitory effect on Staphylococcus aureus, Proteus vulgaris, Bacillus cereus, and Enterobacter aerogenes.	[104]
Skin whitening and Anti- skin wrinkles Activities	BK	Root barks	in vivoin vitro	Zebrafish/B16F10 cells	Kazinol U	0–20 μM	Inhibitory activity of MITF and downstream target genes such as tyrosinase, Tyrp1 and Tyrp2.	[19]
Skin whitening and Anti- skin wrinkles Activities	BK	Stems	in vitro	HEK-293T cells	EtOH extract	0–100 μg/mL	Maintaining the collagen content of the skin by eliminating reactive oxygen species and inhibiting collagenase activity.	[106]
Others	BK	Roots	in vitro	RAW264.7 cells	Broussonol F, G and K	10–30 μM	Inhibiting RANKL-induced osteoclast formation.	[44]
	-	Fruits	in vivo	mice	Chushizi	-	Increasing liver function and alleviating DILI via regulating the TLR3/ JNK/ c-jun/c-fos/JAK/STAT3 pathway.	[107]
	BP	-	in vitro	hHFDP cells	Ethanolic extract	0–20 µg/mL	Regulating β-Catenin and STAT6 target protein.	[108]
	BK	Twigs	in vitro	human umbilical vein endothelial cells	Ethanolic extract	0.1–10 µg/mL	Inhibiting VEGF-A stimulated phosphorylation/activation of ERK, Akt and p70S6K, the downstream targets of the VEGFR-2 signaling pathways, and downregulation of VEGFR-2 and MMP-2.	[109]
	BP	Roots	in vitro	-	8-(1,1-Dimethylallyl)-5′-(3-methylbut-2-enyl)-3′,4′,5,7-tetrahydroxyflanvonol, papyriflavonol A and broussoflavonol B	0–30 µM	Inhibiting hAChE and BChE with IC₅₀^′s ranging from 0.8 to 3.1 μM and from 0.5 to 24.7 μM, respectively.	[47]
	BP	Seeds	in vitro	N1E-115 cells	Chushizilactam A and adenosine	50 µM	Adenosine could obviously increase cAMP.	[73]
	BK	Stems	in vivo	mice	Water extract	-	Water extract has immune-stimulating activity by enhancing the Th1 immune response.	[110]
	BK	-	in vitro	MCF-7 cells	Broussonin A, tupichinol C kazinol U and (+)-(2R) kazinol I	10 µM	Modulating the E2-responsive genes as functional ER ligands such as E2.	[50]
	BK	Roots	in vitro	C2C12 and 10T1/2 cells	Kazinol P	1000 nM	Promoting myogenic differentiation through the activation of p38MAPK and MyoD transcription activities.	[111]
	BK	Root barks	in vivo	RAW 264.7 cells	Kazinol B	6.25–50 µM	Inhibiting the NO synthesis with an IC₅₀ of 21.6 mM	[112]

4. Application

4.1. Supplements to the Diet of Animals

It was reported that a supplement of Broussonetia species in the roughage diet was beneficial to the growth performance, carcass traits, meat quality and color, immune response, digestibility of crude protein, and rumen fermentation in different animals, such as Hu rams and lambs and growing goats [20,119]. Tao et al. [120] demonstrated that beef cattle fed on a diet with 15% BP could enhance their antioxidant functions by decreasing blood 8-OHdG and MDA and increasing blood SOD and TAC; the supplements could strengthen the performance by increasing final BW, ADG, DMI and FCR, improve the meat quality by lowing pH and drip loss and increasing CIE L, and also increase the PUFA and DHA concentrations in meat. A diet supplemented with BP could enhance immune and antioxidant function, as well as increase the polyunsaturated fatty acid concentrations in the milk of Holstein cows [121,122]. A diet supplemented with BP leaf extracts at a certain dosage could increase the growth performance and antioxidant capacity of weaned piglets, enhance immune functions and disease resistance, reduce the occurrence of diarrhea, and affect the composition of fecal microflora [123].

4.2. Phytoremediation of Heavy Metal-Contaminated Soil

The effective phytoremediation of heavy metal-contaminated soil requires species with high metal tolerance. Broussonetia species were excellent choices, owing to their adaptation to drought and to a saline-alkali environment [124]. Zeng et al. [125] showed that BP could effectively alleviate the adverse effects of heavy metal-contaminated soil on plant growth by enhancing the antioxidant enzyme activities in leaves and binding heavy metal-contaminated soil with organic acids, carbohydrates, protein, and amino acids in roots. Huang et al. [126] isolated Bacillus cereus HM5 and Bacillus thuringiensis HM7, and explored their potential to improve the effect of remedying Mn pollution by BP; the results showed that the biomass, total root length, surface area, crossings, tips, forks, and root activity of BP with the two strains were higher than BP without the two strains, so the two strains could promote the accumulation of Mn. Luo et al. [127] indicated that BP could be used for the revegetation and phytostabilization of zinc-smelting slag sites because of the high heavy-metal tolerance and low heavy-metal accumulation. Co-planting was also a sustainable approach for the phytoremediation of the heavy metal-contaminated soil. The hyperaccumulator Pteris vittata L., co-planted with BP, could improve the environmental quality of heavy metal-contaminated soil by promoting the growth and uptake of P. vittata L. and improving the comprehensive extraction of metal [128]. Zeng et al. [129] selected Pteris vittata L., Arundo donax L., Morus alba L. and BP for tree–herb co-planting; the results indicated that the four-herb co-planting system positively affected the soil microbes and had stronger impacts on the composition of soil microorganisms.

4.3. Combination Using

The pharmacological effects of Broussonetia genus are limited but, when combined with other plants, it can exert more meaningful pharmacological effects. A liquid bandage was made from Styela clava tunics and BK barks cellulose powders; it could accelerate wound-healing in the surgical skin wounds of Sprague-Dawley rats by stimulating re-epithelialization and connective tissue formation, without liver or kidney toxicities [23]. A new phytoformula containing BP and Lonicera japonica was revealed to have therapeutic potential for systemic septic inflammation, as well as chronic bronchitis, and against LPS-induced septic inflammation in mice by reducing the induction of some important proinflammatory cytokines, at a dosage of 200–400 mg/kg [22]. Phellinus linteus, cultured with BK, could inhibit melanogenesis by activating the phosphatidylinositol 3-kinase/Akt/glycogen synthase kinase-3beta signaling pathway and down-regulating the microphthalmia-associated transcription factor [130].

4.4. Inhibition of Target Enzymes

Broussonetia species showed inhibitory effects on target enzymes, such as monophenolase and diphenolase of tyrosinase [55], mushroom tyrosinase [31], xanthine oxidase, and protein tyrosine phosphatase 1B (PTP1B) [37]. Four compounds, kazinol S, kazinol C, broussonin C, and kazinol F, isolated from BK roots, showed inhibitory effects on the monophenolase of tyrosinase, with IC₅₀ values ranging between 0.43 and 17.9 µM [55]. They also showed reversible slow-binding inhibitory effects on the diphenolase of tyrosinase, with IC₅₀ values of 22.8, 1.7, 0.57, and 26.9 µM, respectively [55]. Zheng et al. [31] revealed the inhibitory activities of mushroom tyrosinase, using L-tyrosine as a substrate of quercetin, broussoflavonol F, 3,5,7,4′-tetrahydroxy-3′-(2-hydroxy-3-methylbut-3-enyl) flavone, and uralenol, with IC₅₀ values of 96.6, 49.5, 57.8, and 82.3 µM, respectively; the results were better than arbutin, a well-known tyrosinase inhibitor [31]. Broussonetones A-C, three new ent-kaurane-type diterpenes, showed marginal inhibitory effect against tyrosinase and xanthine oxidase, as indicated by Ko et al. [32]. 3,3′,4′,5,7-pentahydroxyflavone, 8-(1,1-dimethylallyl)-5′-(3-methylbut-2-enyl)-3′,4′,5,7-tetrahydroxyflanvonol, uralenol and broussochalcone A showed the in vitro inhibition of PTP1B, as reported by Chen et al. [30]. Broukazinol A, 7,4′-dihydroxy-3′-prenylflavan, Broukazinol C, (2S)-7,3′-dimethoxy-4′-hydroxyflavan, broussonin B, 1-(4-hydroxy-2-methoxyphenyl)-3-(4-hydroxy-3-prenylphenyl) propane and 1-(2,4-dihydroxy-3-prenylphenyl)-3-(4-hydroxyphenyl) propane, isolated from BK twigs, also showed the inhibition of PTP1B, as reported by Xue et al. [37].

4.5. Papermaking and Cloth-Making

The barks of the Broussonetia species were excellent materials for the production of papers and clothes, which can be attributed to the high fiber content of the phloem. Cai Lun papermaking was one of the four great inventions of ancient China; this great invention used BP barks at that time. Notably, the first banknote in the world was made from BP. Papers made by BP barks were once used for making books and for writing in the Tang dynasty and their use continued during the Ming and Qing dynasties, as evidenced by many Dunhuang and Turfan manuscripts [21]. The bark of BP can also be used to make ancient tapa clothes; in this process, the barks were peeled from the cut stems to obtain a long strip, then the manufacturer removed the inner bark and washed and pounded the fibers to flatten them, felted them together with sheets in the sun, and finally printed them with native dyes to produce the finished traditional tapa cloth [10].

4.6. Others

In addition to the applications mentioned above, the remaining applications are classified as “others”. A study conducted by Qiu et al. explored their application in cleaning up phosphorus pollution; they showed that BP biochar, when combined with phosphate in the forms of exchangeable phosphorus, Al-bound phosphorus, and Fe-bound phosphorus, could be used to treat eutrophic bodies of water [131]. Zhang et al. [132] measured the ability of BP to resist drought due to the electrophysiological characteristics of the plants; the results showed that the relative tensity of BP and M. alba were 3.965 and 2.624, respectively. The author also demonstrated that the minimal fluorescence efficiency and maximal photochemical efficiency were 5.496 and 7.640 for BP and 6.577 and 5.359 for M. alba, respectively; therefore, the drought-resistance ability of BP was greater than that of M. alba. Mo et al. [133] studied the ability of BP to control air pollution; the results showed that BP was efficient in capturing small particles and showed high levels of PM accumulation.

5. Conclusions and Further Perspectives

This review mainly summarized the phytochemistry, pharmacology, and applications of the Broussonetia genus. In this work, we present a list of 338 compounds that have been isolated from the herbs of Broussonetia, including 144 flavonoids, 50 phenylpropanoids, 38 polyphenols, 35 alkaloids, 17 terpenoids, 5 steroids, and 49 other metabolites, which indicated that flavonoids were the main constituent in the genus of Broussonetia. A variety of pharmacological activities have been demonstrated in vivo or in vitro assays, including anti-tumor, antioxidant, anti-inflammatory, antidiabetic, anti-obesity, antibacterial, and antiviral properties, as well as skin whitening and anti-wrinkle activities. Nevertheless, some studies of the Broussonetia genus are limited at present.

First, phytochemistry clarified 338 compounds isolated from BP, BK, and BL, but only 5 steroids and 17 terpenoids were involved. Undoubtedly, we can make more effort toward the exploration of steroids and terpenoids by the targeted phytochemical methods. Second, the Broussonetia genus consists of 11 species, but the investigations of phytochemistry, pharmacology and applications were only studied in BP, BK, and BL. Therefore, it is extremely important for researchers to conduct a comprehensive evaluation of other species to extend the available source domain. Third, pharmacological studies have uncovered anti-tumor, antioxidant, anti-inflammatory, anti-diabetic, anti-obesity, antibacterial, and antiviral properties, as well as skin whitening and anti-wrinkle activities. Notably, the relevant bioactive compounds only include flavonoids, penylpropanoids, and polyphenols; therefore, the pharmacological activities of the remaining compounds need to be further explored by researchers. Furthermore, the pharmacological activities of the concrete compounds of crude extracts need to be confirmed in the future, which would be conducive to finding new candidates for corresponding diseases. Fourth, mechanism analysis indicated that active compounds and extracts mainly showed anti-tumor effects by inducing cell apoptosis and triggering cell cycle arrest; they showed anti-inflammatory activity mainly by inhibiting NO production and iNOS expression and showed anti-diabetic effects mainly via blocking the NF-kB pathway and α-glucosidase. Undoubtedly, we can see that mechanism studies of the active compounds and extracts isolated from Broussonetia species were mainly concentrated on the typical targets and pathways. Hence, new targets and pathways should be detected in the future. Fifth, in vitro models were considered to be the main conditions; therefore, more in vivo models should be used to investigate properties in the future. Sixth, although the applications indicated that Broussonetia species could be used to supplement the diet of beef cattle, growing goats, cows, and piglets, and showed multiple beneficial effects on their growth performance, carcass traits, meat quality, and immune response, the concrete clinical safety, toxicity and pharmacokinetics studies for animals and humans were extremely limited; thus, exploring these aspects is the top priority in future research.

Overall, this updated review on the plants of the Broussonetia genus can provide an important and valuable reference for researchers interested in Broussonetia and promote scientific development and utilization of the Broussonetia genus.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/molecules27165344/s1, Figure S1: Chemical structures of the Flavonoids in Broussonetia species, Figure S2: Chemical structures of the Penylpropanoids in Broussonetia species, Figure S3: Chemical structures of the Polyphenols in Broussonetia species, Figure S4: Chemical structures of the Alkaloids in Broussonetia species, Figure S5: Chemical structures of the Terpenoids in Broussonetia species, Figure S6: Chemical structures of the Steroids in Broussonetia species, Figure S7: Chemical structures of the Others in Broussonetia species.

Author Contributions

Y.C. and L.W. contributed equally to this work. Y.C. and L.W.: data curation, writing-original draft and review & editing, methodology. F.W., X.L., Y.A., W.Z. (Wei Zhao), J.T., D.K.: data curation, investigation, formal analysis. W.Z. (Wenru Zhang), Y.X., Y.B.: investigation, methodology, data curation. H.Z. provided the financial support for this manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the Project of the Shandong Province Key Research and Development Program (2021CXGC010511), the project of Shandong postgraduate education quality curriculum (SDYKC21051), and the innovation training program for college students of Shandong University of Traditional Chinese Medicine (2021047, 202255) of Honglei Zhou.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

Abbreviations

CALCBP	Chlorogenic acid-like compounds extracted from BP
MS	Mass Spectrum
NMR	Nuclear Magnetic Resonance Spectrometer
EC	Esophagus cancer
NSCLC	Non-small cell lung cancer cell
ERK	Extracellular signal-regulated kinase
AMPK	Adenosine 5-monophosphate [134]-activated protein kinase
HepG	Human hepatoma carcinoma
CAA	Cellular antioxidant activity
IC₅₀	Half maximal inhibitory concentration
XOD	Xanthine oxidase
TFC	Determination of total flavonoid content
TPC	Determination of total phenolic contents
MTT	3-(4,5)-dimethylthiahiazo (-z-y1)-3,5-di- phenytetrazoliumromide
TBARS	Thiobarbituric acid-reactive substance
PMA	Phorbol 12-myristate 13-acetate
PHA	Phytohemagglutinin
iNOS	Inducible nitric oxide synthas
LPS	Lipopolysaccharide
PA-	Palmitate-
STZ	Streptozotocin
HFD	High fat diet
MLDS	Multiple low-dose streptozotocin
ALT	Alanine aminotransferase
OLETF	Otsuka Long-Evans Tokushima fatty
MIC	Minimum inhibitory concentration
APAP	Acetaminophen
hHFDP	Human hair follicle dermal papilla
BChE	Butylcholinesterase
hAChE	Human acetylcholinesterase
OVA	Ovalbumin
BW	Body weight
ADG	Average daily gain
DMI	Dry matter intake
FCR	Feed conversion ratio
MDA	Malondialdehyde
SOD	Superoxide dismutase
TAC	Total antioxidant capacity
PUFA	Polyunsaturated fatty acids
DHA	Docosahexaenoic acid
LPS	Lipopolysaccharide
PTP1B	Tyrosine phosphatase 1B protein
MAPK	Mitogen-activated protein kinase
STAT	Signal transducer and activator of transcription
JAK	Janus kinase
AD	Atopic dermatitis
T24	Human bladder cancer cells
DPPH	1,1′-diphenyl-2-picryl-hydrazyl radical
ABTS	2,2′-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid
FRAP	Ferric reducing activity power assay
TEAC	Trolox equivalent antioxidant capacity
TNF-alpha	Tumor necrosis factor-alpha
IFN-gamma	Interferongamma
TARC/CCL17	Thymus-and-activation regulated chemokine
MDC/CCL22	Macrophagederived chemokine
RANTES/CCL5	Regulated-onactivation-normal T cell-expressed-and-secreted chemokine
IL-4	Interleukin-4
IgE	Plasma immunoglobulin E
RINm5F cells	Rat pancreatic β-cell line
HFD	Ten-week-high fat diet

References

Wang, F.F.; Su, Y.L.; Chen, N.Z.; Shen, S.H. Genome-Wide analysis of the UGT gene family and identification of flavonoids in Broussonetia papyrifera. Molecules 2021, 26, 3449. [Google Scholar] [CrossRef] [PubMed]
Lee, Y.; Kwon, J.; Jeong, J.H.; Ryu, J.H.; Kim, K. Kazinol C from Broussonetia kazinoki stimulates autophagy via endoplasmic reticulum stress-mediated signaling. Anim. Cells Syst. 2022, 26, 28–36. [Google Scholar] [CrossRef] [PubMed]
Gunatilaka, A.L.; Uvais, M.; Sultanbawa, S.; Surendrakumar, S.; Somanathan, R. Structure of a bipyridine alkaloid from Broussonetia zeylanica. Phytochemistry 1983, 22, 2847–2850. [Google Scholar] [CrossRef]
Casuga, F.P.; Castillo, A.L.; Corpuz, M. GC–MS analysis of bioactive compounds present in different extracts of an endemic plant Broussonetia luzonica (Blanco)(Moraceae) leaves. Asian Pac. J. Trop. Biomed. 2016, 6, 957–961. [Google Scholar] [CrossRef] [Green Version]
Chung, K.F.; Kuo, W.H.; Hsu, Y.H.; Li, Y.H.; Rubite, R.R.; Xu, W.B. Molecular recircumscription of Broussonetia (Moraceae) and the identity and taxonomic status of B. kaempferi var. australis. Bot. Stud. 2017, 58, 11. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Lemmens, R. Broussonetia greveana (Baill.) CC Berg. Plant. Resour. Trop. Afr. 1977, 47, 356. [Google Scholar]
Sun, J.; Liu, S.F.; Zhang, C.S.; Yu, L.N.; Bi, J.; Zhu, F.; Yang, Q.L. Chemical composition and antioxidant activities of Broussonetia papyrifera fruits. PLoS ONE 2012, 7, e32021. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Wang, G.W.; Huang, B.K.; Qin, L.P. The genus Broussonetia: A review of its phytochemistry and pharmacology. Phytother. Res. 2012, 26, 1–10. [Google Scholar] [CrossRef] [PubMed]
Luo, X.; Tian, T.; Tan, X.; Yang, X.J. First report of lasiodiplodia theobromae causing brown leaf spot on Broussonetia papyrifera in Southwestern China. Plant Dis. 2020, 104, 2024. [Google Scholar] [CrossRef] [Green Version]
Whistler, W.A. Broussonetia papyrifera (paper mulberry). Tradit. Tree Initiat. 2006, 9, 1–3. [Google Scholar]
Lin, J.; Zou, J.; Zhang, B.; Que, Q.; Zhang, J.; Chen, X.; Zhou, W. An efficient in vitro propagation protocol for direct organo genesis from root explants of a multi-purpose plant, Broussonetia papyrifera (L.) L’Hér. ex Vent. Woody Forage 2021, 170, 113686. [Google Scholar]
Available online: https://www.plantplus.cn/info/Broussonetia (accessed on 1 July 2022).
Sirita, J.; Chomsawan, B.; Yodsoontorn, P.; Kornochalert, S.; Lapinee, C.; Jumpatong, K. Antioxidant activities, phenolic and tannin contents of paper mulberry (Broussonetia papyrifera) extract. Med. Plants 2020, 12, 371–375. [Google Scholar] [CrossRef]
Vu, N.K.; Le, T.T.; Woo, M.H.; Min, B. Anti-inflammatory and cytotoxic activities of phenolic compounds from Broussonetia kazinoki. Phytochemistry 2021, 27, 176–182. [Google Scholar]
Kim, H.J.; Kim, D.; Yoon, H.; Choi, C.S.; Oh, Y.S.; Jun, H.S. Prevention of oxidative stress-induced pancreatic Beta cell damage by Broussonetia kazinoki Siebold fruit extract via the ERK-Nox4 pathway. Antioxidants 2020, 9, 406. [Google Scholar] [CrossRef] [PubMed]
Cha, J.Y.; Kim, Y.T.; Kim, H.S.; Cho, Y.S. Antihyperglycemic effect of stem bark powder from paper mulberry (Broussonetia kazinoki sieb.) in type 2 diabetic Otsuka long-evans Tokushima fatty rats. J. Med. Food 2008, 11, 499–505. [Google Scholar] [CrossRef]
Geng, C.A.; Yan, M.H.; Zhang, X.M.; Chen, J.J. Anti-oral microbial flavanes from Broussonetia papyrifera under the guidance of bioassay. Nat. Prod. Bioprospect. 2019, 9, 139–144. [Google Scholar] [CrossRef] [Green Version]
Ghosh, R.; Chakraborty, A.; Biswas, A.; Chowdhuri, S. Identification of polyphenols from Broussonetia papyrifera as SARS-CoV-2 main protease inhibitors usingin silicodocking and molecular dynamics simulation approaches. J. Biomol. Struct. Dyn. 2021, 39, 6747–6760. [Google Scholar] [CrossRef]
Lim, J.; Nam, S.; Jeong, J.H.; Kim, M.J.; Yang, Y.; Lee, M.S.; Lee, H.G.; Ryu, J.H.; Lim, J.S. Kazinol U inhibits melanogenesis through the inhibition of tyrosinase-related proteins via AMP kinase activation. Br. J. Pharmacol. 2019, 176, 737–750. [Google Scholar] [CrossRef] [Green Version]
Sheng, P.; He, L.; Ji, S.S.; Huang, J.L.; Zhang, Z.H.; Wang, D.S.; Liu, J.P.; Zhang, H.Q. Effect of Broussonetia papyrifera L. (paper mulberry) on growth performance, carcase traits, meat quality and immune performance in Hu ram lambs. Ital. J. Anim. Sci. 2021, 20, 691–697. [Google Scholar] [CrossRef]
Peng, X.; Liu, H.; Chen, P.; Tang, F.; Hu, Y.; Wang, F.; Pi, Z.; Zhao, M.; Chen, N.; Chen, H. A chromosome-scale genome assembly of paper mulberry (Broussonetia papyrifera) provides new insights into its forage and papermaking usage. Mol. Plant 2019, 12, 661–677. [Google Scholar] [CrossRef]
Ko, H.J.; Kwon, O.S.; Jin, J.H.; Son, K.H.; Kim, H.P. Inhibition of experimental systemic inflammation (septic inflammation) and chronic bronchitis by new phytoformula BL containing Broussonetia papyrifera and Lonicera japonica. Biomol. Ther. 2013, 21, 66–71. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Park, J.J.; Kim, J.E.; Yun, W.B.; Lee, M.R.; Choi, J.Y.; Song, B.R.; Son, H.J.; Lim, Y.; Kang, H.G.; An, B.S.; et al. Therapeutic effects of a liquid bandage prepared with cellulose powders from Styela clava tunics and Broussonetia kazinoki bark: Healing of surgical wounds on the skin of Sprague Dawley rats. Mol. Med. Rep. 2019, 19, 452–460. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Fang, S.C.; Shieh, B.J.; Lin, C.N. Phenolic constituents of formosan Broussonetia-papyrifera. Phytochemistry 1994, 37, 851–853. [Google Scholar]
Fang, S.C.; Shieh, B.J.; Wu, R.R.; Lin, C.N. Isoprenylated flavonols of formosan Broussonetia-papyrifera. Phytochemistry 1995, 38, 535–537. [Google Scholar] [CrossRef]
Lin, C.N.; Chiu, P.H.; Fang, S.C.; Shieh, B.J.; Wu, R.R. Revised structure of broussoflavonol G and the 2D NMR spectra of some related prenylflavonoids. Phytochemistry 1996, 41, 1215–1217. [Google Scholar]
Ko, H.H.; Yen, M.H.; Wu, R.R.; Won, S.J.; Lin, C.N. Cytotoxic isoprenylated flavans of Broussonetia kazinoki. J. Nat. Prod. 1999, 62, 164–166. [Google Scholar] [CrossRef]
Lee, D.; Bhat, K.P.L.; Fong, H.H.S.; Farnsworth, N.R.; Pezzuto, J.M.; Kinghorn, A.D. Aromatase inhibitors from Broussonetia papyrifera. J. Nat. Prod. 2001, 64, 1286–1293. [Google Scholar] [CrossRef]
Zhang, P.C.; Wang, S.; Wu, Y.; Chen, R.Y.; Yu, D.Q. Five new diprenylated flavonols from the leaves of Broussonetia kazinoki. J. Nat. Prod. 2001, 64, 1206–1209. [Google Scholar] [CrossRef]
Chen, R.M.; Hu, L.H.; An, T.Y.; Li, J.; Shen, Q. Natural PTP1B inhibitors from Broussonetia papyrifera. Bioorg. Med. Chem. Lett. 2002, 12, 3387–3390. [Google Scholar] [CrossRef]
Zheng, Z.P.; Cheng, K.W.; Chao, J.F.; Wu, J.J.; Wang, M.F. Tyrosinase inhibitors from paper mulberry (Broussonetia papyrifera). Food Chem. 2008, 106, 529–535. [Google Scholar] [CrossRef]
Ko, H.H.; Chang, W.L.; Lu, T.M. Antityrosinase and antioxidant effects of ent-kaurane diterpenes from leaves of Broussonetia papyrifera. J. Nat. Prod. 2008, 71, 1930–1933. [Google Scholar] [CrossRef]
Ahn, J.H.; Liu, Q.; Lee, C.; Ahn, M.J.; Yoo, H.S.; Hwang, B.Y.; Lee, M.K. A new pancreatic lipase inhibitor from Broussonetia kanzinoki. Bioorg. Med. Chem. Lett. 2012, 22, 2760–2763. [Google Scholar] [CrossRef] [PubMed]
Guo, F.J.; Feng, L.; Huang, C.; Ding, H.X.; Zhang, X.T.; Wang, Z.Y.; Li, Y.M. Prenylflavone derivatives from Broussonetia papyrifera, inhibit the growth of breast cancer cells in vitro and in vivo. Phytochem. Lett. 2013, 6, 331–336. [Google Scholar] [CrossRef]
Ran, X.K.; Wang, X.T.; Liu, P.P.; Chi, Y.X.; Wang, B.J.; Dou, D.Q.; Kang, T.G.; Xiong, W. Cytotoxic constituents from the leaves of Broussonetia papyrifera. Chin. J. Nat. Med. 2013, 11, 269–273. [Google Scholar] [CrossRef]
Yang, C.Y.; Li, F.; Du, B.W.; Chen, B.; Wang, F.; Wang, M.K. Isolation and characterization of new phenolic compounds with estrogen biosynthesis-inhibiting and antioxidation activities from Broussonetia papyrifera leaves. PLoS ONE 2014, 9, e94198. [Google Scholar] [CrossRef] [PubMed]
Xue, J.J.; Lei, C.; Wang, P.P.; Kim, K.Y.; Li, J.Y.; Li, J.; Hou, A.J. Flavans and diphenylpropanes with PTP1B inhibition from Broussonetia kazinoki. Fitoterapia 2018, 130, 37–42. [Google Scholar] [CrossRef] [PubMed]
Li, F.; Wen, T.; Liu, J. Progress in chemical constituents and bioactivities of Broussonetia papyrifera (L.) Vent. Med. Res. 2019, 3, 190005. [Google Scholar] [CrossRef]
Lou, Y.; Su, S.Y.; Li, Y.N.; Lei, C.; Li, J.Y. Flavonoids with PTP1B inhibition from Broussonetia papyrifera. China J. Chin. Mater. Med. 2019, 44, 88–94. [Google Scholar]
Ryu, H.W.; Park, M.H.; Kwon, O.K.; Kim, D.Y.; Hwang, J.Y.; Jo, Y.H.; Ahn, K.S.; Hwang, B.Y.; Oh, S.R. Anti-inflammatory flavonoids from root bark of Broussonetia papyrifera in LPS-stimulated RAW264.7 cells. Bioorg. Chem. 2019, 92, 103233. [Google Scholar] [CrossRef]
Tian, J.L.; Liu, T.L.; Xue, J.J.; Hong, W.; Zhang, Y.; Zhang, D.X.; Cui, C.C.; Liu, M.C.; Niu, S.L. Flavanoids derivatives from the root bark of Broussonetia papyrifera as a tyrosinase inhibitor. Ind. Crops Prod. 2019, 138, 111445. [Google Scholar] [CrossRef]
Malanik, M.; Treml, J.; Lelakova, V.; Nykodymova, D.; Oravec, M.; Marek, J.; Smejkal, K. Anti-inflammatory and antioxidant properties of chemical constituents of Broussonetia papyrifera. Bioorg. Chem. 2020, 104, 104298. [Google Scholar] [CrossRef] [PubMed]
Qureshi, H.; Anwar, T.; Khan, S.; Fatimah, H.; Waseem, M. Phytochemical constituents of Broussonetia papyrifera (L.) L’He’r. ex Vent: An overview. J. of the Indian Chem. Soc. 2020, 97, 55–65. [Google Scholar]
Vu, N.K.; Ha, M.T.; Kim, C.S.; Gal, M.; Kim, J.A.; Woo, M.H.; Lee, J.H.; Min, B.S. Structural characterization of prenylated compounds from Broussonetia kazinoki and their antiosteoclastogenic activity. Phytochemistry 2021, 188, 112791. [Google Scholar] [CrossRef] [PubMed]
Yadav, A. Brousssonetia Papyrifera linn: Deep insights into its dominant pharmacological perspectives. World J. Pharm. Res. 2021, 10, 577–590. [Google Scholar]
Ko, H.H.; Yu, S.M.; Ko, F.N.; Teng, C.M.; Lin, C.N. Bioactive constituents of Morus australis and Broussonetia papyrifera. J. Nat. Prod. 1997, 60, 1008–1011. [Google Scholar] [CrossRef]
Ryu, H.W.; Curtis-Long, M.J.; Jung, S.; Jeong, I.Y.; Kim, D.S.; Kang, K.Y.; Park, K.H. Anticholinesterase potential of flavonols from paper mulberry (Broussonetia papyrifera) and their kinetic studies. Food Chem. 2012, 132, 1244–1250. [Google Scholar] [CrossRef]
Ma, Y.M.; Zhang, Z.W.; Feng, C.L. Flavonoids of Broussonetia papyrifera. Chem. Nat. Compd. 2009, 45, 881–882. [Google Scholar] [CrossRef]
Lee, D.Y.; Lee, H.J.; Ryu, J.H. Prenylated polyphenols from Broussonetia kazinoki as inhibitors of Nitric Oxide production. Molecules 2018, 23, 639. [Google Scholar] [CrossRef] [Green Version]
Lee, D.Y.; Kim, D.H.; Lee, H.J.; Lee, Y.; Ryu, K.H.; Jung, B.I.; Song, Y.S.; Ryu, J.H. New estrogenic compounds isolated from Broussonetia kazinoki. Bioorg. Med. Chem. Lett. 2010, 20, 3764–3767. [Google Scholar] [CrossRef]
Yu, D.; Jing, Q.; Yu, X. Research progress on new chemical constituents and biological activities of Broussonetia papyrifera. Nat. Prod. Res. Dev. 2014, 26, 1327. [Google Scholar]
Venkatesh, K.R.; Chauhan, S. Mulberry: Life enhancer. J. Med. Plants Res. 2008, 2, 271–278. [Google Scholar]
Mei, R.Q.; Wang, Y.H.; Du, G.H.; Liu, G.M.; Zhang, L.; Cheng, Y.X. Antioxidant lignans from the fruits of Broussonetia papyrifera. J. Nat. Prod. 2009, 72, 621–625. [Google Scholar] [CrossRef] [PubMed]
Zhou, X.J.; Mei, R.Q.; Zhang, L.; Lu, Q.; Zhao, J.; Adebayo, A.H.; Cheng, Y.X. Antioxidant phenolics from Broussonetia papyrifera fruits. J. Asian Nat. Prod. Res. 2010, 12, 399–406. [Google Scholar] [CrossRef] [PubMed]
Baek, Y.S.; Ryu, Y.B.; Curtis-Long, M.J.; Ha, T.J.; Rengasamy, R.; Yang, M.S.; Park, K.H. Tyrosinase inhibitory effects of 1,3-diphenylpropanes from Broussonetia kazinoki. Bioorg. Med. Chem. 2009, 17, 35–41. [Google Scholar] [CrossRef]
Ryu, H.W.; Lee, B.W.; Curtis-Long, M.J.; Jung, S.; Ryu, Y.B.; Lee, W.S.; Park, K.H. Polyphenols from Broussonetia papyrifera displaying potent alpha-glucosidase inhibition. J. Agric. Food Chem. 2010, 58, 202–208. [Google Scholar] [CrossRef] [PubMed]
Ryu, H.W.; Lee, J.H.; Kang, J.E.; Jin, Y.M.; Park, K.H. Inhibition of Xanthine Oxidase by phenolic phytochemicals from Broussonetia papyrifera. J. Korean Soc. Appl. Biol. Chem. 2012, 55, 587–594. [Google Scholar] [CrossRef]
Shibano, M.; Kitagawa, S.; Kusano, G. Studies on the constituents of Broussonetia species. 1. Two new pyrrolidine alkaloids, broussonetines C and D, as beta-galactosidase and beta-mannosidase inhibitors from Broussonetia kazinoki SIEB. Chem. Pharm. Bull. 1997, 45, 505–508. [Google Scholar] [CrossRef] [Green Version]
Shibano, M.; Kitagawa, S.; Nakamura, S.; Akazawa, N.; Kusano, G. Studies on the constituents of Broussonetia species. 2. Six new pyrrolidine alkaloids, Broussonetine A, B, E, F and Broussonetinine A and B, as inhibitors of glycosidases from Broussonetia kazinoki SIEB. Chem. Pharm. Bull. 1997, 45, 700–705. [Google Scholar] [CrossRef] [Green Version]
Shibano, M.; Nakamura, S.; Kubori, M.; Minoura, K.; Kusano, G. Studies on the constituents of Broussonetia species. IV. Two new pyrrolidinyl piperidine alkaloids, broussonetines I and J, from Broussonetia kazinoki SIEB. Chem. Pharm. Bull. 1998, 46, 1416–1420. [Google Scholar] [CrossRef] [Green Version]
Shibano, M.; Nakamura, S.; Akazawa, N.; Kusano, G. Studies on the constituents of Broussonetia species. III. Two new pyrrolidine alkaloids, broussonetines G and H, as inhibitors of glycosidase, from Broussonetia kazinoki SIEB. Chem. Pharm. Bull. 1998, 46, 1048–1050. [Google Scholar] [CrossRef] [Green Version]
Shibano, M.; Tsukamoto, D.; Kusano, G. A new pyrrolizidine alkaloid, broussonetine N, as an inhibitor of glycosidase, from Broussonetia kazinoki SIEB and absolute stereostructures of broussonetines A and B. Chem. Pharm. Bull. 1999, 47, 907–908. [Google Scholar] [CrossRef] [Green Version]
Shibano, M.; Nakamura, S.; Motoya, N.; Kusano, G. Studies on the constituents of Broussonetia species. V. Two new pyrrolidine alkaloids, broussonetines K and L, as inhibitors of glycosidase, from Broussonetia kazinoki SIEB. Chem. Pharm. Bull. 1999, 47, 472–476. [Google Scholar] [CrossRef] [Green Version]
Shibano, M.; Tsukamoto, D.; Fujimoto, R.; Masui, Y.; Sugimoto, H.; Kusano, G. Studies on the constituents of Broussonetia species. VII. Four new pyrrolidine alkaloids, broussonetines M, O, P, and Q, as inhibitors of glycosidase, from Broussonetia kazinoki Sieb. Chem. Pharm. Bull. 2000, 48, 1281–1285. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Tsukamoto, D.; Shibano, M.; Okamoto, R.; Kusano, G. Studies on the constituents of Broussonetia species VIII. Four new pyrrolidine alkaloids, broussonetines R, S, T, and V and a new pyrroline alkaloid, broussonetine U, from Broussonetia kazinoki Sieb. Chem. Pharm. Bull. 2001, 49, 492–496. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Pang, S.Q.; Wang, G.Q.; Lin, J.S.; Diao, Y.; Xu, R.A. Cytotoxic activity of the alkaloids from Broussonetia papyrifera fruits. Pharm. Biol. 2014, 52, 1315–1319. [Google Scholar] [CrossRef]
Pang, S.Q.; Wang, G.Q.; Huang, B.K.; Zhang, Q.Y.; Qin, L.P. Isoquinoline alkaloids from Broussonetia papyrifera fruits. Chem. Nat. Compd. 2007, 43, 100–102. [Google Scholar] [CrossRef]
O’Hagan, D. Pyrrole, pyrrolidine, pyridine, piperidine and tropane alkaloids. Nat. Prod. Rep. 2000, 17, 435–446. [Google Scholar] [CrossRef]
Zhong, H.T.; Li, F.; Chen, B.; Wang, M.K. Euphane triterpenes from the bark of Broussonetia papyrifera. Helv. Chim. Acta 2011, 94, 2061–2065. [Google Scholar] [CrossRef]
Liu, F.; Liu, Y.; Yan, Z.; Ma, Y.; Zhai, X.Q. Triterpenes from the bark of Broussonetia papyrifera (L.) Vent. Nat. Prod. Res. Dev. 2011, 40, 120–122. [Google Scholar]
Casuga, F.P.; Castillo, A.L.; Corpuz, M.J. Bioactive compounds and cytotoxicity of ethyl acetate extract from Broussonetia luzonica (Moraceae) blanco leaves against hepatocellular carcinoma (Hepg2) cell lines. Pharmacogn. J. 2016, 8, 497–501. [Google Scholar] [CrossRef] [Green Version]
Feng, W.S.; Li, H.W.; Zheng, X.K.; Chen, S.Q. Two new megastigmane O-glucopyranosides from the leaves of Broussonetia papyrifera. Chin. Chem. Lett. 2007, 18, 1518–1520. [Google Scholar] [CrossRef]
Mei, R.Q.; Wang, X.T.; Chen, R.; Luo, H.R.; Cheng, Y.X. N-containing compounds from Broussonetia papyrifera seeds and their cAMP regulatory activity in N1E-115 cells. Chem. Nat. Compd. 2011, 47, 783–785. [Google Scholar] [CrossRef]
Wang, L.; Son, H.J.; Xu, M.L.; Hu, J.H.; Wang, M.H. Anti-inflammatory and anticancer properties of dichloromethane and butanol fractions from the stem bark of Broussonetia papyrifera. J. Korean Soc. Appl. Biol. Chem. 2010, 53, 297–303. [Google Scholar] [CrossRef]
Li, Y.; Li, H.L.; Zhang, Y.; Li, L.; Qin, C.G. In vitro antioxidant and anticancer activities of the extract from Paper Mulberry (Broussonetia papyrifera L.) fruit. Asian J. Chem. 2013, 25, 5453–5456. [Google Scholar] [CrossRef]
Zhu, Z.X.; Zhao, Y.T. Mechanism of gastric carcinoma cell apoptosis induced by chlorogenic acid-like compounds extracted from Broussonetia papyrifera. Chin. Tradit. Herb. Drugs 2018, 24, 5345–5351. [Google Scholar]
Dou, C.Z.; Liu, Y.F.; Zhang, L.L.; Chen, S.H.; Hu, C.Y.; Liu, Y.; Zhao, Y.T. Polyphenols from Broussonetia papyrifera induce apoptosis of HepG2 cells via inactivation of ERK and AKT signaling pathways. J. Evid. Based Complementary Altern. Med. 2021, 2021, 8841706. [Google Scholar] [CrossRef]
Wei, B.L.; Chen, Y.C.; Hsu, H.Y. Kazinol Q from Broussonetia kazinoki enhances cell death induced by Cu (II) through increased reactive oxygen species. Molecules 2011, 16, 3212–3221. [Google Scholar] [CrossRef]
Guo, M.X.; Wang, M.L.; Zhang, X.T.; Deng, H.; Wang, Z.Y. Broussoflavonol B restricts growth of ER-negative breast cancer stem-like cells. Anticancer Res. 2013, 33, 1873–1879. [Google Scholar]
Park, S.; Fudhaili, A.; Oh, S.S.; Lee, K.W.; Madhi, H.; Kim, D.H.; Yoo, J.; Ryu, H.W.; Park, K.H.; Kim, K.D. Cytotoxic effects of kazinol A derived from Broussonetia papyrifera on human bladder cancer cells, T24 and T24R2. Phytomedicine 2016, 23, 1462–1468. [Google Scholar] [CrossRef]
Jung, Y.C.; Han, S.; Hua, L.; Ahn, Y.H.; Cho, H.; Lee, C.J.; Lee, H.; Cho, Y.Y.; Ryu, J.H.; Jeon, R.; et al. Kazinol-E is a specific inhibitor of ERK that suppresses the enrichment of a breast cancer stem-like cell population. Biochem. Biophys. Res. Commun. 2016, 470, 294–299. [Google Scholar] [CrossRef]
Jung, Y.C.; Han, S.; Hua, L.; Zhao, H.Y.; Lee, C.J.; Cho, Y.Y.; Jeon, R.; Ryu, J.H.; Kim, W.Y. Targeting cancer stem cell through blocking the Erk pathway with Kazinol-E from Broussonetia kazinoki. Cancer Res. 2015, 75, 2600. [Google Scholar] [CrossRef]
Kim, J.H.; Kim, M.S.; Lee, B.H.; Kim, J.K.; Ahn, E.K.; Ko, H.J.; Cho, Y.R.; Lee, S.J.; Bae, G.U.; Kim, Y.K.; et al. Marmesin-mediated suppression of VEGF/VEGFR and integrin beta 1 expression: Its implication in non-small cell lung cancer cell responses and tumor angiogenesis. Oncol. Rep. 2017, 37, 91–97. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Park, S.H.; Lee, J.; Shon, J.C.; Phuc, N.M.; Jee, J.G.; Liu, K.H. The inhibitory potential of Broussochalcone A for the human cytochrome P450 2J2 isoform and its anti-cancer effects via FOXO3 activation. Phytomedicine 2018, 42, 199–206. [Google Scholar] [CrossRef]
Shin, S.; Son, Y.; Liu, K.H.; Kang, W.; Oh, S. Cytotoxic activity of broussochalcone a against colon and liver cancer cells by promoting destruction complex-independent beta-catenin degradation. Food Chem. 2019, 131, 110550. [Google Scholar] [CrossRef] [PubMed]
Jeong, J.H.; Ryu, J.H. Broussoflavonol B from Broussonetia kazinoki Siebold exerts anti-pancreatic cancer activity through downregulating FoxM1. Molecules 2020, 25, 2328. [Google Scholar] [CrossRef] [PubMed]
Wang, Q.; Zhong, S.; Wu, H.; Wu, Q.J.E. In vitro anti-cancer effect of marmesin by suppression of PI3K/Akt pathway in esophagus cancer cells. Esophagus 2022, 19, 163–174. [Google Scholar] [CrossRef] [PubMed]
Kim, H.S.; Lim, J.; Lee, D.Y.; Ryu, J.H.; Lim, J.S. Kazinol C from Broussonetia kazinoki activates AMP-activated protein kinase to induce antitumorigenic effects in HT-29 colon cancer cells. Oncol. Rep. 2015, 33, 223–229. [Google Scholar] [CrossRef] [Green Version]
Xiao, J.Q.; Fang, F.P.; Ying, F.Y.; Ying, Y.T. Ultrasonic extraction and antioxidant activity investigation of Broussonetia papyrifer seed oil. Nat. Prod. Res. Dev. 2014, 26, 1685. [Google Scholar]
Li, Y.; Shang, X.Y.; Niu, W.N.; Xu, C.L.; Qin, C.G. Inhibitory Activity of the Extract from Broussonetia papyrifera Fruits to Cellular Lipid Peroxidation in vitro. Asian J. Chem. 2014, 26, 201–204. [Google Scholar] [CrossRef]
Sun, J.; Zhang, C.S.; Yu, L.N.; Bi, J.; Liu, S.F.; Zhu, F.; Yang, Q.L. Antioxidant activity and total phenolics of Broussonetia papyrifera flower extracts. Appl. Mech. Mater. 2012, 140, 263–267. [Google Scholar] [CrossRef]
Cheng, Z.J.; Lin, C.N.; Hwang, T.L.; Teng, C.M. Broussochalcone A, a potent antioxidant and effective suppressor of inducible nitric oxide synthase in lipopolysaccharide-activated macrophages. Biochem. Pharmacol. 2001, 61, 939–946. [Google Scholar] [CrossRef]
Tsai, F.H.; Lien, J.C.; Lin, L.W.; Chen, H.Y.; Ching, H.; Wu, C.R. Protective effect of Broussonetia papyrifera against Hydrogen Peroxide-induced oxidative stress in SH-SY5Y cells. Biosci. Biotechnol. Biochem. 2009, 73, 1933–1939. [Google Scholar] [CrossRef] [PubMed]
Xu, M.L.; Wang, L.; Hu, J.H.; Lee, S.K.; Wang, M.H. Antioxidant activities and related polyphenolic constituents of the methanol extract fractions from Broussonetia papyrifera stem bark and wood. Food Sci. Biotechnol. 2010, 19, 677–682. [Google Scholar] [CrossRef]
Kwak, W.J.; Moon, T.C.; Lin, C.X.; Rhyn, H.G.; Jung, H.J.; Lee, E.; Kwon, D.Y.; Son, K.H.; Kim, H.P.; Kang, S.S.; et al. Papyriflavonol A from Broussonetia papyrifera inhibits the passive cutaneous anaphylaxis reaction and has a secretory phospholipase A (2)-inhibitory activity. Biol. Pharm. Bull. 2003, 26, 299–302. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Huang, S.P.; Guan, X.; Kai, G.Y.; Xu, Y.Z.; Xu, Y.; Wang, H.J.; Pang, T.; Zhang, L.Y.; Liu, Y. Broussonin E suppresses LPS-induced inflammatory response in macrophages via inhibiting MAPK pathway and enhancing JAK2-STAT3 pathway. Chin. J. Nat. Med. 2019, 17, 372–380. [Google Scholar] [CrossRef]
Lin, L.W.; Chen, H.Y.; Wu, C.R.; Liao, P.M.; Lin, Y.T.; Hsieh, M.T.; Ching, H. Comparison with various parts of Broussonetia papyrifera as to the antinociceptive and anti-inflammatory activities in rodents. Biosci. Biotechnol. Biochem. 2008, 72, 2377–2384. [Google Scholar] [CrossRef] [Green Version]
Lee, J.K.; Ha, H.; Lee, H.Y.; Park, S.J.; Jeong, S.I.; Choi, Y.J.; Shin, H.K. Inhibitory effects of heartwood extracts of Broussonetia kazinoki Sieb on the development of atopic dermatitis in NC/Nga mice. Biosci. Biotechnol. Biochem. 2010, 74, 1802–1806. [Google Scholar] [CrossRef]
Bae, U.J.; Lee, D.Y.; Song, M.Y.; Lee, S.M.; Park, J.W.; Ryu, J.H.; Park, B.H. A prenylated flavan from Broussonetia kazinoki prevents cytokine-induced beta-cell death through suppression of nuclear factor-kappa B activity. Biol. Pharm. Bull. 2011, 34, 1026–1031. [Google Scholar] [CrossRef] [Green Version]
Bae, U.J.; Jang, H.Y.; Lim, J.M.; Hua, L.; Ryu, J.H.; Park, B.H. Polyphenols isolated from Broussonetia kazinoki prevent cytokine-induced beta-cell damage and the development of type 1 diabetes. Exp. Mol. Med. 2015, 47, 739. [Google Scholar] [CrossRef] [Green Version]
Lee, H.; Li, H.; Jeong, J.H.; Noh, M.; Ryu, J.H. Kazinol B from Broussonetia kazinoki improves insulin sensitivity via Akt and AMPK activation in 3T3-L1 adipocytes. Fitoterapia 2016, 112, 90–96. [Google Scholar] [CrossRef]
Lee, J.M.; Choi, S.S.; Park, M.H.; Jang, H.; Lee, Y.H.; Khim, K.W.; Oh, S.R.; Park, J.; Ryu, H.W.; Choi, J.H. Broussonetia papyrifera root bark extract exhibits A7 anti-inflammatory effects on adipose tissue and improves insulin sensitivity potentially via AMPK activation. Nutrients 2020, 12, 773. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Kim, D.; Kim, H.J.; Cha, S.H.; Jun, H.S. Protective effects of Broussonetia kazinoki Siebold fruit extract against palmitate-induced lipotoxicity in mesangial cells. J. Evid. Based Complementary Altern. Med. 2019, 2019, 4509403. [Google Scholar] [CrossRef] [PubMed]
Kumar, N.N.; Ramakrishnaiah, H.; Krishna, V.; Deepalakshmi, A.P. GC-MS analysis and antimicrobial activity of seed oil of Broussonetia papyrifera (L.) VENT. J. Pharm. Sci. Res. 2015, 6, 3954. [Google Scholar]
Park, J.Y.; Yuk, H.J.; Ryu, H.W.; Lim, S.H.; Kim, K.S.; Park, K.H.; Ryu, Y.B.; Lee, W.S. Evaluation of polyphenols from Broussonetia papyrifera as coronavirus protease inhibitors. J. Enzym. Inhib. Med. Chem. 2017, 32, 504–512. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Kwon, B.; Kim, M.H.; Park, I.S.; Choo, Y.M.; Jeong, S.I.; Yu, K.Y.; Kim, J.; Kim, K.S.; Kim, M.S. The potential efficacy of Broussonetia kazinoki stem extract to show antioxidant property or suppress collagenase activity. Biomed. J. Sci. Tech. Res. 2019, 17, 12802–12804. [Google Scholar]
Zhang, Y.D.; Biao, Y.N.; Chu, X.Q.; Hao, L.; Shi, C.; Liu, Y.; Zhang, Y.X.; Wang, X. Protective effect of Chushizi (Fructus Broussonetiae) on acetaminophen-induced rat hepatitis by inhibiting the Toll-like receptor 3/c-Jun N-terminal kinase/c-jun/c-fos/janus protein tyrosine kinase/activators of transcription 3 pathway. J. Tradit. Chin. Med. 2020, 40, 965–973. [Google Scholar]
Lee, Y.H.; Nam, G.; Kim, M.K.; Cho, S.C. Broussonetia papyrifera promotes hair growth through the regulation of β-catenin and STAT6 target proteins: A phototrichogram analysis of clinical samples. Cosmetics 2020, 7, 40. [Google Scholar] [CrossRef]
Cho, Y.R.; Kim, J.H.; Kim, J.K.; Ahn, E.K.; Ko, H.J.; In, J.K.; Lee, S.J.; Bae, G.U.; Kim, Y.K.; Oh, J.S.; et al. Broussonetia kazinoki modulates the expression of VEGFR-2 and MMP-2 through the inhibition of ERK, Akt and p70(S6K)-dependent signaling pathways: Its implication in endothelial cell proliferation, migration and tubular formation. Oncol. Rep. 2014, 32, 1531–1536. [Google Scholar] [CrossRef] [Green Version]
Jung, D.Y.; Ha, H.K.; Lee, H.Y.; Lee, J.A.; Jeong, S.I.; Choi, Y.J.; Shin, H.K. Broussonetia kazinoki Siebold stimulates immune response in ovalbumin-immunized mice. J. Korean Orient. Med. 2011, 32, 10–17. [Google Scholar]
Hwang, J.; Lee, S.J.; Yoo, M.; Go, G.Y.; Lee, D.Y.; Kim, Y.K.; Seo, D.W.; Kang, J.S.; Ryu, J.H.; Bae, G.U. Kazinol-P from Broussonetia kazinoki enhances skeletal muscle differentiation via p38MAPK and MyoD. Biochem. Biophys. Res. Commun. 2015, 456, 471–475. [Google Scholar] [CrossRef]
Ryu, J.H.; Ahn, H.; Lee, H.J. Inhibition of nitric oxide production on LPS-activated macrophages by kazinol B from Broussonetia kazinoki. Fitoterapia 2003, 74, 350–354. [Google Scholar] [CrossRef]
Guo, M.X.; Wang, M.L.; Deng, H.; Zhang, X.T.; Wang, Z.Y. A novel anticancer agent Broussoflavonol B downregulates estrogen receptor (ER)-alpha 36 expression and inhibits growth of ER-negative breast cancer MDA-MB-231 cells. Eur. J. Pharmacol. 2013, 714, 56–64. [Google Scholar] [CrossRef] [PubMed]
Yao, L.; Xiong, L.; Yoo, C.G.; Dong, C.Y.; Meng, X.Z.; Dai, J.; Ragauskas, A.J.; Yang, C.L.; Yu, J.; Yang, H.T.; et al. Correlations of the physicochemical properties of organosolv lignins from Broussonetia papyrifera with their antioxidant activities. Sustain. Energy Fuels 2020, 4, 5114–5119. [Google Scholar] [CrossRef]
Han, Q.H.; Wu, Z.L.; Huang, B.; Sun, L.Q.; Ding, C.B.; Yuan, S.; Zhang, Z.W.; Chen, Y.E.; Hu, C.; Zhou, L.J.; et al. Extraction, antioxidant and antibacterial activities of Broussonetia papyrifera fruits polysaccharides. Int. J. Biol. Macromol. 2016, 92, 116–124. [Google Scholar] [CrossRef] [PubMed]
Huang, L.Z.; Qin, L.P.; Huang, B.K. Antioxidative and anti-inflammatory properties of Chushizi oil from fructus Broussonetiae. J. Med. Plants Res. 2011, 5, 6407–6412. [Google Scholar]
Lee, H.; Ha, H.; Lee, J.K.; Park, S.J.; Jeong, S.I.; Shin, H.K. The leaves of Broussonetia kazinoki Siebold inhibit atopic dermatitis-like response on mite allergen-treated Nc/Nga mice. Biomol. Ther. 2014, 22, 438–444. [Google Scholar] [CrossRef] [Green Version]
Wu, W.T. Evaluation of anti-inflammatory effects of Broussonetia papyrifera stem bark. Indian J. Pharmacol. 2012, 44, 26–30. [Google Scholar] [CrossRef] [Green Version]
Hua, J.L.; Xu, T.F.; Shen, Q.W.; Liu, Y.; Huang, G.J.; Rao, D.J.; Song, C.M.; Wang, J.K. Productive and metabolic increments of the inclusion of Broussonetia papyrifera to replace maize silage in growing goats. Czech J. Anim. Sci. 2020, 65, 303–310. [Google Scholar] [CrossRef]
Tao, H.; Si, B.; Xu, W.; Tu, Y.; Diao, Q.Y. Effect of Broussonetia papyrifera L. silage on blood biochemical parameters, growth performance, meat amino acids and fatty acids compositions in beef cattle. Asian Australas. J. Anim. Sci. 2020, 33, 732. [Google Scholar] [CrossRef]
Hao, Y.Y.; Huang, S.; Si, J.F.; Zhang, J.; Gaowa, N.; Sun, X.G.; Lv, J.Y.; Liu, G.K.; He, Y.Q.; Wang, W.; et al. Effects of Paper Mulberry Silage on the milk production, apparent digestibility, antioxidant capacity, and fecal bacteria composition in holstein dairy cows. Animals 2020, 10, 1152. [Google Scholar] [CrossRef]
Si, B.W.; Tao, H.; Zhang, X.L.; Guo, J.P.; Cui, K.; Tu, Y.; Diao, Q.Y. Effect of Broussonetia papyrifera L. (paper mulberry) silage on dry matter intake, milk composition, antioxidant capacity and milk fatty acid profile in dairy cows. Asian Australas. J. Anim. Sci. 2018, 31, 1259–1266. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Chen, G.S.; Shui, S.Z.; Chai, M.J.; Wang, D.; Su, Y.Y.; Wu, H.B.; Sui, X.D.; Yin, Y.L. Effects of Paper Mulberry (Broussonetia papyrifera) leaf extract on growth performance and fecal microflora of weaned piglets. BioMed. Res. Int. 2020, 2020, 6508494. [Google Scholar] [CrossRef] [PubMed]
Huang, H.M.; Zhao, Y.L.; Xu, Z.G.; Zhang, W.; Jiang, K.K. Physiological responses of Broussonetia papyrifera to manganese stress, a candidate plant for phytoremediation. Ecotoxicol. Environ. Saf. 2019, 181, 18–25. [Google Scholar] [CrossRef] [PubMed]
Zeng, P.; Guo, Z.; Xiao, X.; Zhou, H.; Gu, J.; Liao, B. Tolerance capacities of Broussonetia papyrifera to heavy metal (loid) s and its phytoremediation potential of the contaminated soil. Int. J. Phytorem. 2021, 24, 580–589. [Google Scholar] [CrossRef] [PubMed]
Huang, H.; Zhao, Y.; Fan, L.; Jin, Q.; Yang, G.; Xu, Z. Improvement of manganese phytoremediation by Broussonetia papyrifera with two plant growth promoting (PGP) Bacillus species. Chemosphere 2020, 260, 127614. [Google Scholar] [CrossRef]
Luo, Y.F.; Wu, Y.G.; Qiu, J.; Wang, H.; Yang, L. Suitability of four woody plant species for the phytostabilization of a zinc smelting slag site after 5 years of assisted revegetation. J. Soils Sediments 2019, 19, 702–715. [Google Scholar] [CrossRef]
Zeng, P.; Guo, Z.H.; Xiao, X.Y.; Peng, C.; Huang, B.; Feng, W.L. Complementarity of co-planting a hyperaccumulator with three metal(loid)-tolerant species for metal(loid)-contaminated soil remediation. Ecotoxicol. Environ. Saf. 2019, 169, 306–315. [Google Scholar] [CrossRef]
Zeng, P.; Guo, Z.H.; Xiao, X.Y.; Peng, C. Effects of tree-herb co-planting on the bacterial community composition and the relationship between specific microorganisms and enzymatic activities in metal(loid)-contaminated soil. Chemosphere 2019, 220, 237–248. [Google Scholar] [CrossRef]
Cha, J.Y.; Yang, H.J.; Moon, H.I.; Cho, Y.S. Inhibitory effect and mechanism on melanogenesis from fermented herbal composition for medical or food uses. Food Res. Int. 2012, 45, 225–231. [Google Scholar] [CrossRef]
Qiu, G.Q.; Zhao, Y.L.; Wang, H.; Tan, X.F.; Chen, F.X.; Hu, X.J. Biochar synthesized via pyrolysis of Broussonetia papyrifera leaves: Mechanisms and potential applications for phosphate removal. Environ. Sci. Pollut. Res. 2019, 26, 6565–6575. [Google Scholar] [CrossRef]
Zhang, M.; Wu, Y.; Xing, D.; Zhao, K.; Yu, R. Rapid measurement of drought resistance in plants based on electrophysiological properties. ASABE 2015, 58, 1441–1446. [Google Scholar]
Mo, L.; Ma, Z.Y.; Xu, Y.S.; Sun, F.B.; Lun, X.X.; Liu, X.H.; Chen, J.G.; Yu, X.X. Assessing the capacity of plant species to accumulate particulate matter in Beijing, China. PLoS ONE 2015, 10, e0140664. [Google Scholar] [CrossRef] [PubMed]
Zerrifi, S.E.; Kasrati, A.; Redouane, E.; Tazart, Z.; El Khalloufi, F.; Abbad, A.; Oudra, B.; Campos, A.; Vasconcelos, V. Essential oils from Moroccan plants as promising ecofriendly tools to control toxic cyanobacteria blooms. Ind. Crops Prod. 2020, 143, 111922. [Google Scholar] [CrossRef]

Figure 1. Broussonetia papyrifera (L.) L’Hér. ex Vent. Images A–F show, respectively: the whole plant (A), leaves (B), flowers (C), fruits (D), twigs (E), and seeds (F).

Figure 2. Broussonetia kazinoki Siebold. Images A–F show, respectively: the whole plant (A), leaves (B), flowers (C), fruits (D), twigs (E) and seeds (F) of Broussonetia kazinoki Siebold.

Table 1. Flavonoids isolated from Broussonetia species.

Number	Compounds	Parts	Source	References
1	Gancaonin P	Whole plants	BP	[45]
2	Isolicoflavonol	Whole plants	BP	[27,30,42,44]
3	Lespedezaflavanone C	Whole plants	BP	[45]
4	Vitexin	Leaves	BP	[31,35,44]
5	Apigenin	Leaves	BP/BK	[13,31,35,44]
6	Pinocembrin	Whole plants	BP	[45]
7	Isobavachalcone	Whole plants	BP	[45]
8	4-Hydroxyisolonchocarpin	Roots	BP	[37,44,45]
9	Luteolin	Leaves/twigs	BP	[30,35,44,46]
10	Cosmosiin	Leaves	BP	[35,45]
11	Isoorientin	Leaves	BP	[36,45]
12	Orientin	Leaves	BP	[36,45]
13	2,4,2′,4′-Tetrahydroxychalcone	Whole plants	BP	[43,45]
14	Abyssinone II	Whole plants	BP	[28,45]
15	Uralenol	Roots/twigs/barks	BP	[29,30,33,37,38,44]
16	Papyriflavonol A	Root barks/twigs	BP	[30,33,40,44,47,48]
17	Norartocarpanone	Whole plants	BP	[45]
18	Broussoflavan A	Root barks	BP	[23,39,44,45,49]
19	Dihydrokaempferol	Whole plants	BP/BK	[14,45]
20	Quercetin	Twigs	BP	[31,45]
21	Bavachin	Whole plants	BP	[45]
22	Isovitexin	Leaves	BP	[36,45]
23	Broussofluorenone C	Whole plants	BP	[45]
24	Broussinol	Whole plants	BP	[45]
25	Sulfuretin	Whole plants	BP	[45]
26	Isogemichalcone C	Whole plants	BP	[28,45]
27	Isoliquiritigenin	Twigs	BP	[31,45]
28	Hesperetin	Roots	BK	[14]
29	Eriodictyol	Roots	BK	[14]
30	Chrysoeriol	Roots	BK	[14]
31	Kaempferol	Roots	BK	[14]
32	Broussonol F	Roots	BK	[44]
33	Broussonol G	Roots	BK	[40,44]
34	Broussonol H	Roots	BK	[44]
35	Broussonol I	Roots	BK	[44]
36	Broussonol K	Roots	BK	[44]
37	Kazinol Q	Root barks/branches and twigs	BP/BK	[26,40,41,43]
38	Kazinol A	Roots	BP/BK	[23,39,42,43,50]
39	Broussonol L	Roots	BK	[44]
40	Kazinol B	Roots/branches and twigs	BP/BK	[24,40,42,43,44]
41	Daphnegiravan D	Roots	BK	[44]
42	Broussonol M	Roots	BK	[44]
43	Broussoflavonol A	Roots/branches and twigs	BK/BP	[42,43,44]
44	4,2′-Dihydroxy-4′-methoxychalcone	Roots	BK	[44]
45	Broussonol C	Roots/leaves	BK	[29,44]
46	(2S)-2′,4′-Dihydroxy-2″-(1-hydroxy-1-methylethyl)-dihydrofuro-2,3-h flavanone	Whole plants	BP	[28,43]
47	(2S)-5,7,2′,4′-Tetrahydroxyflavanone	Whole plants	BP	[28,43]
48	(2S)-Euchrenone	Whole plants	BP	[28,43]
49	Broussoflavonol F	Root barks/twigs	BP	[24,27,30,42,49]
50	(2S)-Naringenin	Whole plants	BP	[28,43]
51	Broussoflavonol E	Root barks/twigs	BP	[24,38,42]
52	Broussoflavonol G	Root barks/Whole plants	BP	[25,42,49]
53	Broussoflavonol C	Root barks/Whole plants	BP	[40,43]
54	Broussoflavonol D	Whole plants	BP	[43]
55	4′-O-Methyldavidioside	Whole plants	BP	[43]
56	5,7,3′,4′-Tetrahydroxy-3-methoxy-6-geranylflavone	Whole plants/twigs	BP	[27,38,42]
57	Broussoflavonol B	Whole plants/branches and twigs/root barks	BP	[38,39,41,42]
58	5,7,3′,4′-Tetrahydroxy-6-geranylflavonol	Whole plants	BP	[28,43]
59	5,7,2′,4′-Tetrahydroxy-3-geranylflavone	Whole plants	BP	[28,43]
60	Broussochalcone A	Roots/twigs/barks	BP	[23,29,30,33,37,39,42,48]
61	Broussochalcone B	Roots	BP	[23,42,45,48]
62	(2S)-Abyssinone II	Whole plants	BP	[43]
63	(2S)-7,4′-Dihydroxy-3′-prenylflavan	Whole plants/twigs	BP/BK	[27,36,42]
64	Broussin	Branches and twigs	BP	[42,43]
65	Isoliquiritigenin 2′-methy ether	Whole plants	BP	[43]
66	1,2,4-Dihydroxy-3-(3-methylbut-2-en-1-yl)-phenyl-3-(2,4-dihydroxyphenyl)-propan-1-one	Whole plants	BP	[43]
67	2-{5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxo-3,4-dihydro-2-H-chromen-8-ylamino}-pentanedioic acid	Whole plants	BP	[43]
68	Broussofluorenone B	Roots	BP	[42,48,51]
69	5,7,3′,5′-Tetrahydroxyflavanone	Twigs	BP	[31,43]
70	5,7,3′,4′-Tetrahydroxy-3-methoxyflavone	Twigs	BP	[31,43]
71	8-(1,1-Dimethylallyl)-5′-(3-methylbut-2-enyl)-3′,4′,5,7-tetrahydroxyflanvonol	Root barks/roots/twigs	BP	[29,38,39,42,48]
72	Kazinol E	Roots	BP	[42,45,48]
73	luteolin-7-O-β-D-glucopyranoside	Leaves	BP	[34,37,42,46]
74	Apigenin-7-O-β-D-glucoside	Leaves	BP	[36,43]
75	3′-γ-Hydroxymethyl-(E)-γ-methylallyl-2,4,2′,4′-tetrahydroxychalcone-11′-O-coumarate	Whole plants	BP	[28,43]
76	Broussoaurone A	Root barks	BP	[43,46]
77	Dimethoxy isogemichalcone C	Whole plants	BP	[43]
78	Chrysoriol-7-O-β-D-glucoside	Leaves	BP	[36,43]
79	Iuteoloside	Whole plants	BP	[43]
80	3,4-Dihydroxyisolonchocarpin	Roots	BP	[42,45,48]
81	(2S)-2′,4′-Dihydroxy-2″(1-hydroxy-1-methylethyl)-dihydrofurano-2,3-h-flavanone	Whole plants	BP	[43]
82	5,7,3′,4′-Tetrahydroxy-3-methoxy-8-geranylflavone	Barks	BP	[33,37,42]
83	5,7,3′,4′-Tetrahydroxy-3-methoxy-8,5′-diprenylflavone	Barks/branches and twigs	BP	[33,41,42]
84	Fipsotwin	Branches and twigs	BP	[42]
85	Kazinol N	Branches and twigs	BP	[42]
86	Kazinol M	Branches and twigs	BP	[42]
87	Threo-dadahol B	Branches and twigs	BP	[42]
88	Threo-dadahol A	Branches and twigs	BP	[42]
89	Broussoflavonol H	Root barks	BP	[41]
90	Broussoflavonol I	Root barks	BP	[41]
91	Broussoflavonol J	Root barks	BP	[41]
92	Broussoflavonol K	Root barks	BP	[41]
93	Glycyrrhiza flavonol A	Root barks	BP	[41]
94	Isolicofavonol	Root barks	BP	[41]
95	Broussoflavonol F	Root barks	BP	[41]
96	Broussoflavonol B	Root barks	BP	[41]
97	(2R)-7,3′,4′-Trihydroxy-6-prenylflavanone	Root barks	BP	[40]
98	Broussochalcone C	Root barks	BP	[40]
99	Broussoflavanonol A	Root barks	BP	[40]
100	Broussonol D	Root barks/leaves/twigs	BP/BK	[28,38,39]
101	Daphnegiravan H	Root barks	BP	[40]
102	(-)-(2S)-Kazinol I	Root barks	BP	[40]
103	Broupapyrin A	Twigs	BP	[39]
104	8-Prenylquercetin-3-methyl ether	Twigs	BP	[39]
105	4,2′,4′-Trihydroxychalcone	Twigs	BP	[39]
106	Butein	Twigs	BP	[39]
107	Broussonol E	Twigs	BP	[39]
108	7,4′-Dihydroxy-3′-prenylflavan	Whole plants	BP	[38]
109	7,3′-Dihydroxy-4′-methoxyflavan	Twigs	BP/BK	[37,38]
110	3′-(3-Methylbut-2-enyl)-3′,4′,7-trihydroxyflavane	Twigs/roots	BP	[29,30,37,42,48,52]
111	Brossoflurenone A	Roots	BP	[38,47]
112	Brossoflurenone B	Roots	BP	[38,47]
113	Apigenin-7-O-β-D-glucopyranoside	Leaves	BP	[38,48]
114	Apigenin-6-C-β-D-glucopyranside	Leaves	BP	[34,37,42]
115	Bropapyrifero	Whole plants	BP	[17]
116	(−)-Broukazinol A	Twigs	BK	[37]
117	(+)-Broukazinol A	Twigs	BK	[37]
118	(2R)-7,4′-Dihydroxy-3′-prenylflavan	Twigs	BK	[37]
119	(2R)-7,4′-Dihydroxyflavan(tupichinol C)	Twigs/root barks/stem barks	BK	[26,32,36]
120	(2S)-7,4′-Dihydroxyflavan(demethylbroussin)	Twigs/root barks/stem barks	BK	[26,32,36]
121	Broussoside F	Twigs	BK	[37]
122	(2S)-7,3′-Dimethoxy-4′-hydroxyflavan	Twigs	BK	[37]
123	Kazinol I	Twigs/root barks	BK	[37,49]
124	Tupichinol C	Root barks	BK	[49,50]
125	Kazinol U	Root barks	BK	[49,50]
126	3,5,7,4′-Tetrahydroxy-3′-(2-hydroxy-3-methylbut-3-enyl) flavone	Twigs	BP	[31,51]
127	Luteoloside	Leaves	BP	[36]
128	Broussoflavonol B	Barks	BP	[34]
129	3′,7-Dihydroxy-4′-methoxyflavan	Stem barks	BK	[33]
130	3,7-Dihydroxy-4′-methoxyflavone	Stem barks	BK	[33]
131	3,7,3′-Trihydroxy-4′-methoxyflavone	Stem barks	BK	[33]
132	(+) − (2R) Kazinol I	Whole plants	BK	[50]
133	Apigenin-7-O--glucopyranoside	Leaves	BP	[32]
134	Amentoflavone	Leaves	BP	[32]
135	3,3′,4′,5,7-Pentahydroxyflavone	Roots	BP	[30]
136	Broussonol A	Leaves	BK	[29]
137	Broussonol B	Leaves	BK	[29]
138	Broussonol E	Leaves	BK	[29]
139	2,4,2′,4′-Tetrahydroxy-3′-prenylchalcone	Whole plants	BP	[28]
140	(2S)-2′,4′-Dihydroxy-7-methoxy-8-prenylflavan	Whole plants	BP	[28]
141	Australone A	Root barks	BP	[52]
142	Cyclomorusin	Whole plants	BP	[26]
143	Cycloartomunin	Whole plants	BP	[26]
144	Dihydroisocycloartomunin	Whole plants	BP	[26]

Table 2. Penylpropanoids isolated from Broussonetia species.

Number	Compounds	Parts	Source	References
145	Marmesin	Whole plants	BP	[45]
146	Graveolone	Whole plants	BP	[45]
147	Sesquineolignan	Whole plants	BP	[45]
148	Dihydrosyringin	Leaves	BP	[36,45]
149	Coniferyl alcohol	Fruits	BP	[43,45,54]
150	Ferulic acid	Fruits	BP	[45,54]
151	p-Coumaraldehyde	Fruits	BP	[45,54]
152	Liriodendrin	Leaves	BP	[35,45]
153	Dihydro-coniferyl alcohol	Whole plants	BP	[45]
154	Chushizisin G	Fruits	BP	[45,53]
155	Chushizisin H	Fruits	BP	[45,53]
156	Pinoresinol	Roots	BK	[14]
157	3′-Hydroxymarmesin-1′-O-β-glucopyranosyl	Roots	BK	[14]
158	Marmesinin	Roots	BK	[14]
159	Syringaresinol-4-O-β-D-glucopyranoside	Roots	BP/BK	[14,38]
160	Rutaretin methylether	Roots	BK	[44]
161	Fipsomin	Roots	BK	[44]
162	(S)-Marmesin	Branches and twigs	BP	[42]
163	(+)-Marmesin	Whole plants	BP	[43]
164	(+)-Pinoresinol-4′-O-β-D-glucopyranosyl-4″-O-β-D-apiofuranoside	Leaves	BP	[35,43]
165	Syringaresinol-4′-O-β-D-glucoside	Leaves	BP	[36,43]
166	Pinoresinol-4′-O-β-D-glucopyranoside	Leaves	BP	[36,43]
167	(S)-8-Methoxymarmesin	Branches and twigs	BP	[42,43]
168	7,8-Dihydroxy-6-(3-methylbut-2-en-1yl)-2H-chromen-2-one	Root barks	BP	[41,43]
169	Broussocoumarin A	Root barks	BP	[41,43]
170	Cissyringin	Fruits	BP	[43,54]
171	Cisconiferin	Fruits	BP	[43,54]
172	Chushizisin A	Fruits	BP	[43,53]
173	Chushizisin B	Fruits	BP	[43,53]
174	Chushizisin C	Fruits	BP	[43,53]
175	Chushizisin D	Fruits	BP	[43,53]
176	Chushizisin E	Fruits	BP	[43,53]
177	Chushizisin F	Fruits	BP	[43,53]
178	p-Coumaric acid	Leaves	BP	[36,43]
179	Threo-1-(4-hydroxy-3-methoxyphenyl)-2-{4-(E)-3-hydroxy-1-propenyl-2-methoxyphenoxy}-1,3-propanediol	Fruits	BP	[43,53]
180	Erythro-1-(4-hydroxyphenyl) glycerol	Fruits	BP	[43,54]
181	Threo-1-(4-hydroxyphenyl) glycerol	Fruits	BP	[43,54]
182	Erythro-1-(4-hydroxy-3-methoxyphenyl)-2-{4-(E)-3-hydroxy-1-propenyl-2-methoxy-phenoxy}-1,3-propanediol	Fruits	BP	[43,53]
183	3-2-(4-Hydroxyphenyl)-3-hydroxymethyl-2,3-dihydro-1-benzofuran-5-ylpropan-1-ol	Fruits	BP	[43,53]
184	Chushizisin I	Fruits	BP	[43,53]
185	6,7-Dimethoxycoumarin	Whole plants	BP	[38]
186	(+)-(2′S,3′R)-3-Hydroxyl marmesin	Whole plants	BP	[38]
187	Iariciresinol-9-O-β-D-glucopyranoside	Whole plants	BP	[38]
188	3,4′,5′-Trihy- droxy-5-methoxy-6H-benzo [c] chromen-6-one	Whole plants	BP	[38]
189	Alternariol-4′-O-methyl ether	Whole plants	BP	[38]
190	Alternariol-5-O-methyl ether	Whole plants	BP	[38]
191	Alternariol	Whole plants	BP	[38]
192	Alternuene	Whole plants	BP	[38]
193	(7S,7′S,7″R,8R,8′R,8″S)-3′-Methoxy-4,4″,9″- trihydroxy- 4′,7″,7,9′,7′,9-triepoxy-5′,8″,8,8″-sesquineolignan	Whole plants	BP	[51]
194	Dihydroconiferyl alcohol	Fruits	BP	[54]

Table 3. Polyphenols isolated from Broussonetia species.

Number	Compounds	Parts	Source	References
195	Broussonin A	Twigs/stem barks/root barks/whole plants	BP/BK	[28,33,37,40,45,49,50]
196	Broussonin B	Twigs/stem barks/root barks	BP/BK	[33,37,40,45]
197	Resveratrol	Whole plants	BP	[45]
198	Moracin N	Whole plants	BP	[28,43,45]
199	Demethylmoracin I	Whole plants	BP	[28,45]
200	Mulberrofuran G	Whole plants	BP	[45]
201	Curculigoside C	Fruits	BP	[45,54]
202	Protocatechuic acid	Whole plants	BP	[45]
203	Kazinol K	Roots/root barks	BK	[27,44]
204	Kazinol F	Twigs/leaves/root barks	BP/BK	[29,37,40,43,55]
205	1-(2,4-Dihydroxyphenyl)-3-(4-hydroxyphenyl)-propane	Whole plants	BP	[28,43]
206	1-(4-Hydroxy-2-methoxyphenyl)-3-(4-hydroxy-3-prenylphenyl)-propane	Twigs/whole plants	BP/BK	[28,37,43]
207	Broussonin C	Root barks	BP/BK	[43,55]
208	Moracin I	Whole plants	BP	[43]
209	Moracin D	Whole plants	BP	[43]
210	Broussonin F	Twigs	BP/BK	[37,43]
211	Moracin M	Whole plants	BP	[43]
212	Broussonin E	Roots	BP/BK	[43,44]
213	3,5,4′-Trihydroxy-bibenzyl-3-O-β-D-glucoside	Leaves	BP	[35,43]
214	Broussoside D	Leaves	BP	[36,43]
215	Broussofluorenone A	Roots	BP	[43,56]
216	Kazinol V	Roots/root barks	BP/BK	[40,44]
217	Kazinol J	Root barks/leaves	BP/BK	[29,40]
218	Kazinol W	Root barks	BP	[40]
219	Altertoxin IV	Whole plants	BP	[38]
220	Altertoxin I	Whole plants	BP	[38]
221	Broukazinol B	Twigs	BK	[37]
222	Broukazinol C	Twigs	BK	[37]
223	1-(2,4-Dihydroxy-3-prenylphenyl)-3-(4-hydroxyphenyl)-propane	Twigs/whole plants	BK/BP	[28,37]
224	Kazinol S	Twigs/root barks	BK	[37,55]
225	Kazinol C	Root barks/twigs	BP/BK	[31,49,55]
226	Kazinol D	Root barks/twigs	BP/BK	[27,31,49,55]
227	(7′R,8′S) -3-Methoxy-4′,9,9″-trihydroxy-4,7′-epoxy-5,8′-neolignan	Whole plants	BP	[51]
228	(7R,8S,8′R)-7″,8″-Threo-3′-methoxy-7′-oxo-4,4″,7″,9,9″-pentahydroxy-4′,8″: 7,9′-bis-epoxy-8,8′-sesquineolignan	Fruits	BP	[51,54]
229	Broussonone A	Stem barks/roots	BP/BK	[33,57]
230	3,4-Dihydroxybenzoic acid	Fruits	BP	[54]
231	Kazinol T	Root barks	BK	[55]
232	Albanol A	Whole plants	BP	[28]

Table 4. Alkaloids isolated from Broussonetia species.

Number	Compounds	Parts	Source	References
233	Liriodenine	Fruits	BP	[45,67]
234	Isoterihanine	Whole plant	BP	[45]
235	Chelerythrine	Whole plants	BP	[45]
236	Oxyavicine	Fruits	BP	[45,67]
237	Broussonpapyrine	Fruits	BP	[45,67]
238	Nitidine	Fruits	BP	[43,67]
239	2′-Deoxyuridine	Whole plants	BP	[43]
240	2′-Deoxyadenosine	Whole plants	BP	[43]
241	Thymidine	Whole plants	BP	[43]
242	N-Norchelerythrine	Fruits	BP	[66]
243	Dihydrosanguinarine	Fruits	BP	[66]
244	Broussonetine R	Branches	BK	[65]
245	Broussonetine S	Branches	BK	[65]
246	Broussonetine T	Branches	BK	[65]
247	Broussonetine U	Branches	BK	[65]
248	Broussonetine V	Branches	BK	[65]
249	Broussonetine M	Branches	BK	[64]
250	Broussonetine O	Branches	BK	[64]
251	Broussonetine P	Branches	BK	[64]
252	Broussonetine Q	Branches	BK	[64]
253	Broussonetine A	Branches	BK	[59,68]
254	Broussonetinine A	Branches	BK	[59,68]
255	Broussonetine B	Branches	BK	[59,68]
256	Broussonetinine B	Branches	BK	[59,68]
257	Broussonetine C	Branches	BK	[58,68]
258	Broussonetine E	Branches	BK	[59,68]
259	Broussonetine D	Branches	BK	[58,68]
260	Broussonetine F	Branches	BK	[59,68]
261	Broussonetine G	Branches	BK	[61,68]
262	Broussonetine H	Branches	BK	[61,68]
263	Broussonetine I	Branches	BK	[60,68]
264	Broussonetine J	Branches	BK	[60,68]
265	Broussonetine K	Branches	BK	[63,68]
266	Broussonetine L	Branches	BK	[63,68]
267	Broussonetine N	Branches	BK	[62]

Table 5. Terpenoids isolated from Broussonetia species.

Number	Compounds	Parts	Source	References
268	Lupeol acetate	Whole plants	BP	[38]
269	Augustic acid	Whole plants	BP	[38]
270	3β-acetoxy–tirucalla-7-en-24S,25-diol	Barks	BP	[38,70]
271	Lupeol	Barks	BP	[70]
272	β-Amyrin	Barks	BP	[70]
273	α-Amyrin acetate	Barks	BP	[70]
274	(3β)-3-(acetyloxy)-eupha-7,25-dien-24-one	Barks	BP	[38,69]
275	(3β,24R)-3-(acetyloxy)–eupha-7,25-dien-24-ol	Barks	BP	[38,69]
276	(3β,24S)-eupha-7,25-diene-3,24-diol	Barks	BP	[38,69]
277	(3β,24R)-Eupha-7,25-diene3,24-diol	Barks	BP	[69]
278	Taraxerol acetate	Leaves	BP	[32]
279	Broussonetone A	Leaves	BP	[32,51]
280	Broussonetone B	Leaves	BP	[32,51]
281	Broussonetone C	Leaves	BP	[32,51]
282	Oleanolic acid	Root barks	BP/BK	[27,38]
283	Squalene	Fruits/root barks/leaves	BP/BL	[25,45,53,71]
284	Butyrospermol acetate	Whole plants	BP	[24]

Table 6. Steroids isolated from Broussonetia species.

Number	Compounds	Parts	Source	References
285	Fucosterol	Whole plants	BP	[45]
286	Ergosterol peroxide	Whole plants	BP	[45]
287	β-Sitosterol	Whole plants	BP	[43]
288	β-Daucosterol	Whole plants	BP	[43]
289	Ergosta-4,6,8,22-tetraen-3-one	Whole plants	BP	[43]

Table 7. Other compounds isolated from Broussonetia species.

Number	Compounds	Parts	Source	References
290	Arbutin	Whole plants	BP	[45]
291	Broussoside B	Whole plants	BP	[45]
292	D-Galacitol	Whole plants	BP	[43]
293	Daucosterol palmitate	Whole plants	BP	[38]
294	Palmitic acid ethyl ester	Whole plants	BP	[38]
295	Palmitic acid	Whole plants	BP	[38]
296	Linoleic acid	Whole plants	BP	[38]
297	9-Octadecenoic acid	Whole plants	BP	[38]
298	8,11-Octadecadienoic acid	Whole plants	BP	[38]
299	α-Monopalmitin	Whole plants	BP	[38]
300	Monoheptadecanoin	Whole plants	BP	[38]
301	Heptadecanoic acid	Whole plants	BP	[38]
302	Phytol	Whole plants/leaves	BP/BL	[38,71]
303	Physcion	Whole plants	BP	[38]
304	Altersolanol A	Whole plants	BP	[38]
305	Altersolanol C	Whole plants	BP	[38]
306	δ-Tocopherol	Whole plants	BP	[38]
307	(4R,5S,10S)-8,9,10-Trihydroxy-4-[3′-methoxy-4′-hydroxyphenyl]-1,6-dioxaspiro [4,5] decan-2-one	Whole plants	BP	[38]
308	4-Hydroxyacetophenone	Whole plants	BP	[38]
309	Erythro-1-(4-hydroxyphenyl)-2-{4-[(E)-3-hydroxy-1-propenyl]-2-methoxyphenoxy}-1,3-propanediol	Whole plants	BP	[51]
310	Threo-1-(4-hydroxyphenyl)-2-{4-[(E)-3-hydroxy1-propenyl]-2-methoxyphenoxy}-1,3-propanediol	Whole plants	BP	[51]
311	threo-1-(4-hydroxyphenyl)-2-[4-(3-hydroxy-1-propyl)-2-methoxyphenoxy]-1,3-propanediol	Whole plants	BP	[51]
312	erythro-1-(4-hydroxyphenyl)-2-[4-(3-hydroxy-1-propyl)-2-methoxyphenoxy]-1,3-propanediol	Whole plants	BP	[51]
313	(7′R,8′S)-3-Methoxy-7-oxo-4′,9,9″-trihydroxy-4,7′-epoxy-5,8′-neolignan	Whole plants	BP	[51]
314	(7′R,8′S)-3-Methoxy-4′,9,9″-trihydroxy-4,7′-epoxy-5,8′-neolignan	Whole plants	BP	[51]
315	Benzyl benzoate-2,6-di-O-β-D-glucopyranoside	Whole plants	BP	[51]
316	Broussoside A	Twigs/leaves	BP/BK	[36,37,43]
317	Broussoside C	Leaves	BP	[36,43]
318	Broussoside E	Leaves	BP	[36,43]
319	Flacourtin	Leaves	BP	[36,45]
320	Poliothyrsoside	Leaves	BP	[36,45]
321	Adenosine	Seeds	BP	[73]
322	Chushizilactam A	Seeds	BP	[73]
323	Arbutine	Fruits	BP	[54]
324	4-Hydroxybenzaldehyde	Fruits	BP	[43,45,54]
325	Curculigoside I	Fruits	BP	[43,54]
326	2-(4-Hydroxyphenyl) propane-1,3-diol-1-O-β-D-glucopyranoside	Fruits	BP	[43,54]
327	(2R,3R,5R,6S,9R)-3-Hydroxy-5,6-epoxyb-ionol-2-O-β-D-glucopyranoside	Leaves	BP	[43,72]
328	(2R,3R,5R,6S,9R)-3-Hydroxyl-5,6-epoxy-acety-b-ionol-2-O-β-D-glucopyranoside	Leaves	BP	[72]
329	Lignoceric acid	Root barks	BP	[25,45]
330	Octacosan-1-ol	Root barks	BP	[25,45]
331	4′-Hydroxycis-cinnamic acid octacosyl ester	Root barks	BP	[25]
332	Erythrinasinate	Root barks	BP	[25]
333	1,2,3-Propanetriol, monoacetate	Leaves	BL	[71]
334	1,2,3-Propanetriol, diacetate	Leaves	BL	[71]
335	Hexadecanoic acid, ethyl ester	Leaves	BL	[71]
336	9,12,15-Octadecatrienoic acid, methyl ester, (Z, Z, Z)-	Leaves	BL	[71]
337	9,12,15-Octatrienoic acid, ethyl ester, (Z, Z, Z)-	Leaves	BL	[71]
338	3,7,11,15-Tetramethyl-2-hexadecen-1-ol	Leaves	BL	[71]

Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

© 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).

Share and Cite

MDPI and ACS Style

Chen, Y.; Wang, L.; Liu, X.; Wang, F.; An, Y.; Zhao, W.; Tian, J.; Kong, D.; Zhang, W.; Xu, Y.; et al. The Genus Broussonetia: An Updated Review of Phytochemistry, Pharmacology and Applications. Molecules 2022, 27, 5344. https://doi.org/10.3390/molecules27165344

AMA Style

Chen Y, Wang L, Liu X, Wang F, An Y, Zhao W, Tian J, Kong D, Zhang W, Xu Y, et al. The Genus Broussonetia: An Updated Review of Phytochemistry, Pharmacology and Applications. Molecules. 2022; 27(16):5344. https://doi.org/10.3390/molecules27165344

Chicago/Turabian Style

Chen, Yueru, Lu Wang, Xue Liu, Fulin Wang, Ying An, Wei Zhao, Jinli Tian, Degang Kong, Wenru Zhang, Yang Xu, and et al. 2022. "The Genus Broussonetia: An Updated Review of Phytochemistry, Pharmacology and Applications" Molecules 27, no. 16: 5344. https://doi.org/10.3390/molecules27165344

APA Style

Chen, Y., Wang, L., Liu, X., Wang, F., An, Y., Zhao, W., Tian, J., Kong, D., Zhang, W., Xu, Y., Ba, Y., & Zhou, H. (2022). The Genus Broussonetia: An Updated Review of Phytochemistry, Pharmacology and Applications. Molecules, 27(16), 5344. https://doi.org/10.3390/molecules27165344

Article Menu

The Genus Broussonetia: An Updated Review of Phytochemistry, Pharmacology and Applications

Abstract

1. Introduction

2. Phytochemistry

2.1. Flavonoids

2.2. Penylpropanoids

2.3. Polyphenols

2.4. Alkaloids

2.5. Terpenoids and Steroids

2.6. Other Compounds

3. Pharmacology

3.1. Anti-Tumor

3.2. Anti-Oxidant Activity

3.3. Anti-Inflammation

3.4. Anti-Diabetic and Anti-Obesity Effects

3.5. Antibacterial and Antiviral Effects

3.6. Skin Whitening and Anti-Wrinkle Activities

3.7. Other Properties

4. Application

4.1. Supplements to the Diet of Animals

4.2. Phytoremediation of Heavy Metal-Contaminated Soil

4.3. Combination Using

4.4. Inhibition of Target Enzymes

4.5. Papermaking and Cloth-Making

4.6. Others

5. Conclusions and Further Perspectives

Supplementary Materials

Author Contributions

Funding

Institutional Review Board Statement

Informed Consent Statement

Data Availability Statement

Conflicts of Interest

Abbreviations

References

Share and Cite

Article Metrics

Article Access Statistics

Further Information

Guidelines

MDPI Initiatives

Follow MDPI