CHEBI:75673 - (−)-epigallocatechin-(4β→6)-(+)-catechin

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ChEBI Name (−)-epigallocatechin-(4β→6)-(+)-catechin
ChEBI ID CHEBI:75673
ChEBI ASCII Name (-)-epigallocatechin-(4beta->6)-(+)-catechin
Definition A proanthocyanidin consisting of (−)-epigallocatechin and (+)-catechin units joined by a (4α→6)-linkage.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information ChemicalBook:CB21387988, ZINC000006090922
Download Molfile XML SDF
Formula C30H26O13
Net Charge 0
Average Mass 594.51960
Monoisotopic Mass 594.13734
InChI InChI=1S/C30H26O13/c31-12-6-16(34)23-22(7-12)43-30(11-4-18(36)27(40)19(37)5-11)28(41)25(23)24-17(35)9-21-13(26(24)39)8-20(38)29(42-21)10-1-2-14(32)15(33)3-10/h1-7,9,20,25,28-41H,8H2/t20-,25+,28+,29+,30+/m0/s1
InChIKey SNJZSALXDDQVRR-DJUYLCBNSA-N
SMILES O[C@H]1Cc2c(O[C@@H]1c1ccc(O)c(O)c1)cc(O)c([C@@H]1[C@@H](O)[C@H](Oc3cc(O)cc(O)c13)c1cc(O)c(O)c(O)c1)c2O
Roles Classification
Biological Role(s): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
Application(s): astringent
A compound that causes the contraction of body tissues, typically used to reduce bleeding from minor abrasions.
(via tannin )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing (−)-epigallocatechin-(4β→6)-(+)-catechin (CHEBI:75673) has functional parent (−)-epigallocatechin (CHEBI:42255)
(−)-epigallocatechin-(4β→6)-(+)-catechin (CHEBI:75673) has functional parent (+)-catechin (CHEBI:15600)
(−)-epigallocatechin-(4β→6)-(+)-catechin (CHEBI:75673) has role metabolite (CHEBI:25212)
(−)-epigallocatechin-(4β→6)-(+)-catechin (CHEBI:75673) is a biflavonoid (CHEBI:50128)
(−)-epigallocatechin-(4β→6)-(+)-catechin (CHEBI:75673) is a hydroxyflavan (CHEBI:72010)
(−)-epigallocatechin-(4β→6)-(+)-catechin (CHEBI:75673) is a polyphenol (CHEBI:26195)
(−)-epigallocatechin-(4β→6)-(+)-catechin (CHEBI:75673) is a proanthocyanidin (CHEBI:26267)
Registry Number Type Source
9464607 Reaxys Registry Number Reaxys
Last Modified
25 November 2013