(-)-arctigenin (Q4787603)

mass

372.157 dalton

1 reference

Arctigenin (English)

5 October 2016

2 references

(3S,4R)-4-[(3,4-dimethoxyphenyl)methyl]-3-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one

inferred from InChI

1 reference

(3R,4S)-3alpha-(3-Methoxy-4-hydroxybenzyl)-4-(3,4-dimethoxybenzyl)-4,5-dihydro-2(3H)-furanone

inferred from InChI

1 reference

inferred from InChI

chemical formula

C₂₁H₂₄O₆

1 reference

Arctigenin (English)

5 October 2016

COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)OC

1 reference

Arctigenin (English)

5 October 2016

COC1=C(C=C(C=C1)C[C@H]2COC(=O)[C@@H]2CC3=CC(=C(C=C3)O)OC)OC

1 reference

Hepatoprotective dibenzylbutyrolactone lignans of Torreya nucifera against CCl4-induced toxicity in primary cultured rat hepatocytes

Arctigenin (English)

5 October 2016

3 references

Potent inhibition of lipopolysaccharide-inducible nitric oxide synthase expression by dibenzylbutyrolactone lignans through inhibition of I-kappaBalpha phosphorylation and of p65 nuclear translocation in macrophages

Neuroprotective dibenzylbutyrolactone lignans of Torreya nucifera

Carthamus tinctorius

2 references

Conjugated serotonins and phenolic constituents in safflower seed (Carthamus tinctorius L.).

Conjugated Serotonins and Phenolic Constituents in Safflower Seed (Carthamus tinctoriusL.)

Forsythia koreana

3 references

Phenolic compounds from Forsythia leaves

Studies on the Methods for Chemical Identification of Forsythiae Fructus and Plantaginis Herba

A Phenylethanoid Glycoside and Other Constituents from the Fruits of Forsythia koreana

Forsythia viridissima

4 references

Phenolic compounds from Forsythia leaves

Studies on the Methods for Chemical Identification of Forsythiae Fructus and Plantaginis Herba

[Application of supercritical fluid extraction to components of crude drugs and plants. II. Extraction of coumarins, lignans and prenylflavonoids]

Anti-inflammatory activity of arctigenin from Forsythiae Fructus

Forsythia suspensa

2 references

Studies on the Methods for Chemical Identification of Forsythiae Fructus and Plantaginis Herba

Characterization of phenolic compounds in the fruits of Forsythia suspensa by high-performance liquid chromatography coupled with electrospray ionization tandem mass spectrometry.

Ipomoea cairica

3 references

Lignan production by Ipomoea callus from carbohydrates

Lignan production by Ipomoea cairica callus cultures

Dibenzylbutyrolactone lignans and coumarins from Ipomoea cairica

Daphne feddei

1 reference

Phenylpropanoids from Daphne feddei and their inhibitory activities against NO production

Taiwania cryptomerioides

1 reference

Cytotoxicity of extractives from Taiwania cryptomerioides heartwood

Anthriscus sylvestris

1 reference

A fast and simple GC MS method for lignan profiling in Anthriscus sylvestris and biosynthetically related Plant species

9 references

A butyrolactone lignan dimer from Arctium lappa

Cytotoxic components of bardanae fructus (goboshi).

Studies on differentiation inducers. VI. Lignan derivatives from Arctium fructus. (2)

Stereochemical diversity in lignan biosynthesis of Arctium lappa L.

Identification of arctigenin as an antitumor agent having the ability to eliminate the tolerance of cancer cells to nutrient starvation

Antiproliferative and apoptotic effects of butyrolactone lignans from Arctium lappa on leukemic cells

Studies on Differentiation-Inducers from Arctium Fructus.

Bupleurum salicifolium

2 references

Structural elucidation and conformational analysis of new lignan butenolides from the leaves of bupleurum salicifolium.

Busaliol and Busalicifol, Two New Tetrahydrofuran Lignans from Bupleurum salicifolium

Centaurea calcitrapa

2 references

Chemical constituents of Centaurea cadmea

Sesquiterpene lactones and lignans from Centaurea species

Centaurea

1 reference

Sesquiterpene lactones from Centaurea tweediei

Centaurea macrocephala

1 reference

Flavonoid C-glucosides and a lignan from Centaurea macrocephala (Compositae)

Centaurea nigra

1 reference

Dibenzylbutyrolactone lignans and indole alkaloids from the seeds of Centaurea nigra (Asteraceae)

Centaurea paui

1 reference

New Sesquiterpene Lactones and Other Constituents fromCentaurea paui

Centaurea regia

1 reference

Palmitic acid ester of sitosteryl 3β-glucoside from Centaurea regia

Centaurea scabiosa

1 reference

Centaurea scabiosa: a source of dibenzylbutyrolactone lignans

Centaurea scoparia

1 reference

Constituents of the Egyptian Centaurea scoparia. III. Phenolic constituents of the aerial parts

Centaurea solstitialis

2 references

Guaianolides and lignans from Centaurea solstitialis subs Schouwii

Sesquiterpene lactones from Centaurea solstitialis

Cynara cardunculus

1 reference

Constituents of Cynara cardunculus

Forsythia ovata

1 reference

Phenolic compounds from Forsythia leaves. II.

Haplophyllum patavinum

1 reference

Production of Lignans by Haplophyllum patavinum in vivo and in vitro

Haplophyllum ptilostylum

1 reference

Further Compounds fromHaplophyllum ptilostylum

Jurinella moschus

1 reference

Sesquiterpene lactones from Jurinella moschus

Oenanthe aquatica

1 reference

Rapid monitoring of biologically-active substances in medicinal plants by tandem mass spectrometry--the identification of lignans in Oenanthe aquatica Lam

Onopordum acaulon

1 reference

Sesquiterpenes, flavonoids and lignans from Onopordon acaulon

Onopordum laconicum

1 reference

Sesquiterpene lactones from Onopordon laconicum and O. sibthorpianum

Saussurea candicans

1 reference

Guaianolides from Saussurea candicans

Saussurea gossypiphora

1 reference

Chemical Constituents of Saussurea eopygmaea

Saussurea medusa

2 references

Immunosuppressive constituents from Saussurea medusa

Anti-tumor-promoting activity of lignans from the aerial part of Saussurea medusa.

Saussurea parviflora

1 reference

Eudesmane derivatives and other constituents from Saussurea parviflora

Saussurea salicifolia

3 references

Further guaianolides from Hymenopappus species

Lignans inhibit cell growth via regulation of Wnt/beta-catenin signaling.

Further guaianolides from saussurea species.

Torreya jackii

1 reference

Lignans from Torreya jackii identified by stopped-flow high-performance liquid chromatography–nuclear magnetic resonance spectroscopy

Trachelospermum axillare

1 reference

Lignans from Trachelospermum axillare

Centaurea arenaria

1 reference

Bioactivity-guided isolation of antiproliferative compounds from Centaurea arenaria.

Vitis vinifera

1 reference

Lignans in selected wines

Centaurea melitensis

1 reference

Americanin, a bioactive dibenzylbutyrolactone lignan, from the seeds of Centaurea americana

Centaurea americana

1 reference

Americanin, a bioactive dibenzylbutyrolactone lignan, from the seeds of Centaurea americana

Centaurea cineraria

1 reference

Acetylenes and other constituents from Centaurea species

Centaurea dealbata

1 reference

Acetylenes and other constituents from Centaurea species

Psephellus dealbatus

1 reference

Acetylenes and other constituents from Centaurea species

Centaurea deflexa

1 reference

Anti-proliferative activity of aguerin B and a new rare nor-guaianolide lactone isolated from the aerial parts of Centaurea deflexa

Centaurea phrygia

1 reference

Flavones and other constituents from Centaurea species

Psephellus schischkinii

1 reference

Isolation, structure elucidation and bioactivity of schischkiniin, a unique indole alkaloid from the seeds of Centaurea schischkinii

Saussurea involucrata

1 reference

Three new lignans from the seeds of Saussurea involucrata

Saussurea laniceps

1 reference

Chemical Constituents of Saussurea eopygmaea

Polla

1 reference

Determination of lignans in edible and nonedible parts of pomegranate (Punica granatum L.) and products derived therefrom, particularly focusing on the quantitation of isolariciresinol using HPLC-DAD-ESI/MSn

Centaurea glomerata

1 reference

Sesquiterpene lactones from Centaurea glomerata

Tripterygium wilfordii

1 reference

Isolation and characterization of a glycosyltransferase with specific catalytic activity towards flavonoids from Tripterygium wilfordii

Onopordum boissierianum

1 reference

Sesquiterpene lactones from Onopordon laconicum and O. sibthorpianum

Identifiers

InChI

InChI=1S/C21H24O6/c1-24-18-7-5-13(11-20(18)26-3)8-15-12-27-21(23)16(15)9-14-4-6-17(22)19(10-14)25-2/h4-7,10-11,15-16,22H,8-9,12H2,1-3H3/t15-,16+/m0/s1

1 reference

Arctigenin (English)

5 October 2016

2 references

Arctigenin (English)

5 October 2016

ChEBI release 2020-09-01

2 references

(-)-Arctigenin (English)

5 October 2016

https://commonchemistry.cas.org/detail?cas_rn=7770-78-7

10 April 2021

1 reference

(−)-Arctigenin (English)

5 October 2016

2 references

Arctigenin (English)

5 October 2016

ChEBI ID

mapping relation type

2 references

(-)-Arctigenin (English)

5 October 2016

International Chemical Identifier

InChI

InChI=1S/C21H24O6/c1-24-18-7-5-13(11-20(18)26-3)8-15-12-27-21(23)16(15)9-14-4-6-17(22)19(10-14)25-2/h4-7,10-11,15-16,22H,8-9,12H2,1-3H3/t15-,16+/m0/s1

1 reference

ARCTIGENIN (English)

5 October 2016

2 references

1 reference

MassBank accession ID

MSBNK-RIKEN-PR303917

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

splash10-0ai0-0009000000-a28beb6b42b572235e38

0 references

DSSTox substance ID

DTXSID60998919

1 reference

DSSTOX compound identifier

0 references

0 references

1 reference

Human Metabolome Database ID

HMDB0030087

2 references

reason for deprecated rank

KNApSAcK ID

C00000609

cannot be confirmed by other sources

1 reference

ChEBI

ChEBI ID

Global Substance Registration System

(-)-Arctigenin (English)

5 October 2016

2 references

UNII

U76MR9VS6M

ARCTIGENIN (English)

5 October 2016

2FD8L150E7

1 reference

0 references

1 reference

(-)-Arctigenin (English)