(Q4690888)

(-)-Epiafzelechin (English)

6 October 2016

2 references

inferred from InChIKey

1 reference

1 reference

C₁₅H₁₄O₅

1 reference

(-)-Epiafzelechin (English)

6 October 2016

canonical SMILES

C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC=C(C=C3)O)O

1 reference

(-)-Epiafzelechin (English)

6 October 2016

isomeric SMILES

C1[C@H]([C@H](OC2=CC(=CC(=C21)O)O)C3=CC=C(C=C3)O)O

1 reference

Cytotoxic phenolic constituents from the root of Actinidia chinensis

(-)-Epiafzelechin (English)

6 October 2016

1 reference

1 reference

Tsuga chinensis

1 reference

A-Study of the Constituents of the Bark ofTsuga Chinensis Pritz. Var. Formosana(Hay.)

Ficus cordata

1 reference

Antimicrobial activity of the crude extracts and compounds from Ficus chlamydocarpa and Ficus cordata (Moraceae).

Typha capensis

5 references

Typhaphthalide and typharin, two phenolic compounds from Typha capensis

Typhaphthalide and typharin, two phenolic compounds from Typha capensis

Typhaphthalide and Typharin, Two Phenolic Compounds from Typha capensis.

Typhaphthalide and typharin, two phenolic compounds from Typha capensis

Typhaphthalide and typharin, two phenolic compounds from Typha capensis

Xanthoceras sorbifolia

2 references

Inhibitory effects on HIV-1 protease of constituents from the wood of Xanthoceras sorbifolia.

Inhibitory effects on HIV-1 protease of constituents from the wood of Xanthoceras sorbifolia.

Calophyllum apetalum

2 references

Prenylated xanthonoids from Calophyllum apetalum

Prenylated xanthonoids from Calophyllum apetalum

2 references

2 references

1 reference

Chemical Examination of the Seeds of Cassia spectablis

Celastrus paniculatus

1 reference

Antioxidant benzoylated flavan-3-ol glycoside from Celastrus orbiculatus.

Crateva religiosa

1 reference

(−)-Epiafzelechin 5-O-βD-glucoside from crataeva religiosa

Larix gmelinii

1 reference

Procyanidins and polyphenols of Larix gmelini bark

Madhuca pasquieri

1 reference

Chemical Constituents of Madhuca pasquiery

Aiouea hammeliana

1 reference

Chemical and Biological Extractives of Lauraceae Species in Costa Rican Tropical Forests

Phyllanthus emblica

2 references

Phyllanemblinins A-F, new ellagitannins from Phyllanthus emblica

Phyllanemblinins A-F, new ellagitannins from Phyllanthus emblica

Bauhinia racemosa

1 reference

Galactolipids from Bauhinia racemosa as a new class of antifilarial agents against human lymphatic filarial parasite, Brugia malayi.

Cassia sieberiana

2 references

Epiafzelechin from the Root Bark of Cassia sieberiana: Detection by DART Mass Spectrometry, Spectroscopic Characterization, and Antioxidant Properties

Epiafzelechin from the Root Bark of Cassia sieberiana: Detection by DART Mass Spectrometry, Spectroscopic Characterization, and Antioxidant Properties

Artocarpus dadah

1 reference

Constituents of the bark and twigs of Artocarpus dadah with cyclooxygenase inhibitory activity

Artocarpus lacucha

1 reference

Constituents of the bark and twigs of Artocarpus dadah with cyclooxygenase inhibitory activity

Wisteria floribunda

2 references

Chemical Components from the Fruit Peels of Wisteria floribunda and their Effects on Rat Aortic Vascular Smooth Muscle Cells

A new flavan-3-ol and the anti-inflammatory effect of flavonoids from the fruit peels of Wisteria floribunda.

Ziziphus jujuba

1 reference

Proanthocyanidins ofZiziphus jujuba

Phanera vahlii

1 reference

Galactolipids from Bauhinia racemosa as a new class of antifilarial agents against human lymphatic filarial parasite, Brugia malayi.

broad bean

1 reference

UHPLC-ESI-QTOF-MS-based metabolic profiling of Vicia faba L. (Fabaceae) seeds as a key strategy for characterization in foodomics

Celastrus orbiculatus

1 reference

(-)-Epiafzelechin: cyclooxygenase-1 inhibitor and anti-inflammatory agent from aerial parts of Celastrus orbiculatus

Xanthoceras sorbifolium

1 reference

Inhibitory effects on HIV-1 protease of constituents from the wood of Xanthoceras sorbifolia.

Camellia sinensis

4 references

1H and13C NMR Assignments of Some Green Tea Polyphenols

Identification of two novel proanthocyanidins in green Tea

Eucalyptus acmenoides

1 reference

Corymbia bleeseri

1 reference

Corymbia calophylla

1 reference

Eucalyptus camaldulensis

1 reference

Eucalyptus crebra

1 reference

Corymbia dichromophloia

1 reference

Corymbia terminalis

1 reference

Corymbia gummifera

1 reference

Eucalyptus haemastoma

1 reference

Corymbia maculata

1 reference

Corymbia papuana

1 reference

Eucalyptus pilularis

1 reference

Corymbia polycarpa

1 reference

Eucalyptus racemosa

1 reference

Eucalyptus signata

1 reference

Eucalyptus saligna

1 reference

Eucalyptus ovata

1 reference

Eucalyptus tereticornis

1 reference

Corymbia tessellaris

1 reference

Eucalyptus tetrodonta

1 reference

InChI=1S/C15H14O5/c16-9-3-1-8(2-4-9)15-13(19)7-11-12(18)5-10(17)6-14(11)20-15/h1-6,13,15-19H,7H2/t13-,15-/m1/s1

Commons category

Epiafzelechin

0 references

Identifiers

InChI

1 reference

(-)-Epiafzelechin (English)

6 October 2016

2 references

(-)-Epiafzelechin (English)

6 October 2016

ChEBI release 2020-09-01

CAS Registry Number

24808-04-6

1 reference

CAS (formerly Chemical Abstracts Service)

25 January 2022

1 reference

Afzelechin (English)

6 October 2016

2 references

(-)-Epiafzelechin (English)

6 October 2016

Reaxys registry number

4236089

1 reference

(-)-epiafzelechin (English)

6 October 2016

ChEBI ID

31028

mapping relation type

2 references

(-)-epiafzelechin (English)

6 October 2016

International Chemical Identifier

InChI

InChI=1S/C15H14O5/c16-9-3-1-8(2-4-9)15-13(19)7-11-12(18)5-10(17)6-14(11)20-15/h1-6,13,15-19H,7H2/t13-,15-/m1/s1

1 reference

EPIAFZELECHIN (2R,3R)(-) (English)

6 October 2016

2 references

inferred from InChIKey

splash10-004r-0695000000-637596f924f8a9ca5e88

1 reference

0 references

splash10-004r-0695000000-23e966644f035c8edce2

0 references

splash10-000i-0950000000-448d487876e279a2e7bb

0 references

DSSTox substance ID

DTXSID201316359

1 reference

Human Metabolome Database ID

1 reference

HMDB0030822

2 references

based on heuristic

inferred from InChIKey

UNII

ZWG9VB324Z

1 reference

0 references

1 reference

http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download

(-)-epiafzelechin (English)

6 October 2016

1 reference