4'-methyl-epigallocatechin (Q27138593)

CHEMBL485460 (English)

ent-Gallocatechin 4'-methyl ether

7 October 2016

stereoisomer of

4'-O-methylgallocatechin

1 reference

based on heuristic

inferred from InChI

1 reference

based on heuristic

inferred from InChI

chemical formula

C₁₆H₁₆O₇

1 reference

CHEMBL485460 (English)

20 November 2016

canonical SMILES

COC1=C(C=C(C=C1O)C2C(CC3=C(C=C(C=C3O2)O)O)O)O

1 reference

CHEMBL485460 (English)

20 November 2016

isomeric SMILES

COC1=C(C=C(C=C1O)[C@@H]2[C@@H](CC3=C(C=C(C=C3O2)O)O)O)O

1 reference

Isolation of tingenone and pristimerin from Maytenus chuchuhuasca

CHEMBL485460 (English)

20 November 2016

2 references

Antinociceptive activity of Maytenus rigida stem bark

Crossopetalum gaumeri

1 reference

Cytotoxic cardenolides and antibacterial terpenoids from Crossopetalum gaumeri

Elaeodendron balae

1 reference

Flavonoids from Elaeodendron balae root bark

Flemingia macrophylla

1 reference

A flavonol C-glycoside from Moghania macrophylla

Vantanea peruviana

1 reference

Flavan-3-ols isolated from some medicinal plants inhibiting COX-1 and COX-2 catalysed prostaglandin biosynthesis

Monteverdia laevis

2 references

Chemical constituents from the Colombian medicinal plant Maytenus laevis

Chemical constituents from the Colombian medicinal plant Maytenus laevis

Parapiptadenia rigida

2 references

Catechin derivatives from Parapiptadenia rigida with in vitro wound-healing properties.

Catechin derivatives from Parapiptadenia rigida with in vitro wound-healing properties.

Helionides oblonga

1 reference

Antidiabetic principles of natural medicines. IV. Aldose reductase and qlpha-glucosidase inhibitors from the roots of Salacia oblonga Wall. (Celastraceae): structure of a new friedelane-type triterpene, kotalagenin 16-acetate

Elaeodendron croceum

1 reference

Flavanoids and triterpenoids from Cassine papillosa and the absolute configuration of 11,11-dimethyl-1,3,8,10-tetra-hydroxy-9-methoxypeltogynan

Salacia oblonga

1 reference

Antidiabetic principles of natural medicines. IV. Aldose reductase and qlpha-glucosidase inhibitors from the roots of Salacia oblonga Wall. (Celastraceae): structure of a new friedelane-type triterpene, kotalagenin 16-acetate

Gymnosporia heterophylla

1 reference

Dihydroagarofuran alkaloid and triterpenes from Maytenus heterophylla and Maytenus arbutifolia

Arabidopsis thaliana

1 reference

Antioxidant, gene expression and metabolomics fingerprint analysis of Arabidopsis thaliana treated by foliar spraying of ZnSe quantum dots and their growth inhibition of Agrobacterium tumefaciens

Monteverdia aquifolium

1 reference

Constituintes químicos das flores de Pterogyne nitens (Caesalpinioideae)

Identifiers

InChI

InChI=1S/C16H16O7/c1-22-16-11(19)2-7(3-12(16)20)15-13(21)6-9-10(18)4-8(17)5-14(9)23-15/h2-5,13,15,17-21H,6H2,1H3/t13-,15-/m1/s1

1 reference

CHEMBL485460 (English)

20 November 2016

2 references

CHEMBL485460 (English)

20 November 2016

ChEBI release 2020-09-01

CAS Registry Number

17291-05-3

1 reference

Global Substance Registration System

UNII

WM87TQ077U

4'-methyl-epigallocatechin (English)

20 November 2016

1 reference

Ourateacatechin (English)

20 November 2016

2 references

CHEMBL485460 (English)

20 November 2016

ChEBI ID

70253

mapping relation type

2 references

CHEMBL485460 (English)

20 November 2016

International Chemical Identifier

InChI

InChI=1S/C16H16O7/c1-22-16-11(19)2-7(3-12(16)20)15-13(21)6-9-10(18)4-8(17)5-14(9)23-15/h2-5,13,15,17-21H,6H2,1H3/t13-,15-/m1/s1

1 reference

CHEMBL485460 (English)

20 November 2016

1 reference

1 reference

DSSTOX compound identifier

DTXCID201366778

0 references

Human Metabolome Database ID

HMDB0303923

2 references

based on heuristic

inferred from InChIKey

UNII

WM87TQ077U

2 references

Global Substance Registration System

UNII

WM87TQ077U

4'-methyl-epigallocatechin (English)

20 November 2016

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

1 reference