Fang et al., 2022 - Google Patents
Identification, potency evaluation, and mechanism clarification of α-glucosidase inhibitors from tender leaves of Lithocarpus polystachyus RehdFang et al., 2022
- Document ID
- 1743604491700431515
- Author
- Fang H
- Liu M
- Li S
- Song W
- Ouyang H
- Xiao Z
- Zhu H
- Publication year
- Publication venue
- Food Chemistry
External Links
Snippet
Lithocarpus polystachyus Rehd. known as Sweet Tea in China has attracted lots of interest for its good hypoglycemic effect and the potential as a hypoglycemic agent. Based on affinity separation-UPLC-Q-TOF-MS/MS, 54 potential α-glucosidase inhibitiors were identified and …
- 241001633106 Lithocarpus 0 title abstract description 32
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/25—Araliaceae (Ginseng family), e.g. ivy, aralia, schefflera or tetrapanax
- A61K36/258—Panax (ginseng)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/70—Polygonaceae (Buckwheat family), e.g. spineflower or dock
- A61K36/704—Polygonum, e.g. knotweed
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/47—Euphorbiaceae (Spurge family), e.g. Ricinus (castorbean)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Fang et al. | Identification, potency evaluation, and mechanism clarification of α-glucosidase inhibitors from tender leaves of Lithocarpus polystachyus Rehd | |
Kumar et al. | Enzymes inhibition and antidiabetic effect of isolated constituents from Dillenia indica | |
Bhandari et al. | α-Glucosidase and α-amylase inhibitory activities of Nepalese medicinal herb Pakhanbhed (Bergenia ciliata, Haw.) | |
Manaharan et al. | Flavonoids isolated from Syzygium aqueum leaf extract as potential antihyperglycaemic agents | |
Melzig et al. | Investigations of the mechanism of membrane activity of selected triterpenoid saponins | |
Kowalski | Studies of selected plant raw materials as alternative sources of triterpenes of oleanolic and ursolic acid types | |
JP4880479B2 (en) | Composition comprising Xantoceros sorbifolia extract, compound isolated from said extract, method of preparing it, and method of use thereof | |
Vujanović et al. | Biological activity of extracts of traditional wild medicinal plants from the Balkan Peninsula | |
Borges et al. | Inhibition of α-glucosidase by flavonoids of Cymbopogon citratus (DC) Stapf | |
Kiziltas et al. | Comprehensive metabolic profiling of Acantholimon caryophyllaceum using LC–HRMS and evaluation of antioxidant activities, enzyme inhibition properties and molecular docking studies | |
Chen et al. | Phytochemical analysis, UPLC-ESI-Orbitrap-MS analysis, biological activity, and toxicity of extracts from Tripleurospermum limosum (Maxim.) Pobed | |
Anand et al. | Phytometabolomic analysis of boiled rhizome of Nymphaea nouchali (Burm. f.) using UPLC-Q-TOF-MSE, LC-QqQ-MS & GC–MS and evaluation of antihyperglycemic and antioxidant activities | |
Liu et al. | Total biflavonoids extraction from Selaginella chaetoloma utilizing ultrasound-assisted deep eutectic solvent: Optimization of conditions, extraction mechanism, and biological activity in vitro | |
Chen et al. | Camellia nitidissima Chi leaf as pancreatic lipase inhibitors: Inhibition potentials and mechanism | |
Fais et al. | Selected enzyme inhibitory effects of Euphorbia characias extracts | |
Yang et al. | Phenolics from Sterculia nobilis Smith pericarp by-products delay carbohydrate digestion by uncompetitively inhibiting α-glucosidase and α-amylase | |
Huang et al. | Comparative assessment of extraction, composition, and in vitro antioxidative properties of wheat bran polyphenols | |
Park et al. | Rapid identification of isoprenylated flavonoids constituents with inhibitory activity on bacterial neuraminidase from root barks of paper mulberry (Broussonetia papyrifera) | |
Zengin et al. | Gathering scientific evidence for a new bioactive natural ingredient: The combination between chemical profiles and biological activities of Flueggea virosa extracts | |
Sancheti et al. | Screening of Korean medicinal plant extracts for α-glucosidase inhibitory activities | |
Asaad et al. | Hepatoprotective effect of kaempferol glycosides isolated from Cedrela odorata L. leaves in albino mice: involvement of Raf/MAPK pathway | |
Taşkın et al. | The influence of different extraction methods/solvents on composition, biological activities and ADMET predictions of phenolics in Tribulus terrestris | |
Chu et al. | Semisynthesis, biological activities, and mechanism studies of Mannich base analogues of magnolol/honokiol as potential α-glucosidase inhibitors | |
Mourabit et al. | HPLC-DAD-ESI/MS phytochemical investigation, antioxidant, and antidiabetic activities of Moroccan Rosa canina L. extracts | |
Li et al. | Protective effects of five compounds from Livistona chinensis R. Brown leaves against hypoxia/reoxygenation, H2O2, or adriamycin-induced injury in H9c2 cells |