ChemFOnt: Showing chemical card for Epicatechin-(2beta->7,4beta->8)-[epicatechin-(4beta->8)]2-catechin (CFc000281453)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-14 03:32:51 UTC

Chemfont ID

CFc000281453

Molecule Identification

Common Name

Epicatechin-(2beta->7,4beta->8)-[epicatechin-(4beta->8)]2-catechin

Definition

Epicatechin-(2beta->7,4beta->8)-[epicatechin-(4beta->8)]2-catechin is a member of the class of compounds known as biflavonoids and polyflavonoids. Biflavonoids and polyflavonoids are organic compounds containing at least two flavan/flavone units. These units are usually linked through CC or C-O-C bonds. Some examples include C2-O-C3, C2-O-C4, C3'-C3''', and C6-C8''. Epicatechin-(2beta->7,4beta->8)-[epicatechin-(4beta->8)]2-catechin is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Epicatechin-(2beta->7,4beta->8)-[epicatechin-(4beta->8)]2-catechin can be found in lingonberry, which makes epicatechin-(2beta->7,4beta->8)-[epicatechin-(4beta->8)]2-catechin a potential biomarker for the consumption of this food product.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
Epicatechin-(2b->7,4b->8)-[epicatechin-(4b->8)]2-catechin	Generator
Epicatechin-(2β->7,4β->8)-[epicatechin-(4β->8)]2-catechin	Generator

Chemical Formula

C₆₀H₄₈O₂₄

Average Molecular Weight

1153.0087

Monoisotopic Molecular Weight

1152.253552464

IUPAC Name

(1R,5R,6R,7S,13S,21R)-5,13-bis(3,4-dihydroxyphenyl)-7-[(2R,3R,4S)-2-(3,4-dihydroxyphenyl)-4-[(2R,3S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-8-yl]-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-8-yl]-4,12,14-trioxapentacyclo[11.7.1.0²,¹¹.0³,⁸.0¹⁵,²⁰]henicosa-2(11),3(8),9,15(20),16,18-hexaene-6,9,17,19,21-pentol

Traditional Name

CAS Registry Number

114715-46-7

SMILES

O[C@H]1CC2=C(O[C@@H]1C1=CC=C(O)C(O)=C1)C([C@@H]1[C@@H](O)[C@H](OC3=C1C(O)=CC(O)=C3[C@@H]1[C@@H](O)[C@H](OC3=C1C(O)=CC1=C3[C@@H]3[C@@H](O)[C@@](OC4=C3C(O)=CC(O)=C4)(O1)C1=CC(O)=C(O)C=C1)C1=CC(O)=C(O)C=C1)C1=CC=C(O)C(O)=C1)=C(O)C=C2O

InChI Identifier

InChI=1S/C60H48O24/c61-23-13-34(71)42-40(14-23)83-60(22-4-8-28(65)33(70)12-22)59(79)50(42)47-41(84-60)18-38(75)46-49(52(78)55(82-58(46)47)21-3-7-27(64)32(69)11-21)45-37(74)17-36(73)44-48(51(77)54(81-57(44)45)20-2-6-26(63)31(68)10-20)43-35(72)16-29(66)24-15-39(76)53(80-56(24)43)19-1-5-25(62)30(67)9-19/h1-14,16-18,39,48-55,59,61-79H,15H2/t39-,48-,49-,50+,51+,52+,53+,54+,55+,59+,60-/m0/s1

InChI Key

ZFOZLANYTWCMKZ-ZQUBELEPSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as biflavonoids and polyflavonoids. These are organic compounds containing at least two flavan/flavone units. These units are usually linked through CC or C-O-C bonds. Some examples include C2-O-C3, C2-O-C4, C3'-C3''', and C6-C8''.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Biflavonoids and polyflavonoids

Direct Parent

Biflavonoids and polyflavonoids

Alternative Parents

Substituents

C-type proanthocyanidin
B-type proanthocyanidin
A-type proanthocyanidin
Bi- and polyflavonoid skeleton
Proanthocyanidin
Catechin
Pyranoflavonoid
3'-hydroxyflavonoid
Flavan-3-ol
3-hydroxyflavonoid
4'-hydroxyflavonoid
5-hydroxyflavonoid
Hydroxyflavonoid
7-hydroxyflavonoid
Flavan
Pyranochromene
Chromane
Benzopyran
1-benzopyran
Catechol
1-hydroxy-4-unsubstituted benzenoid
Ketal
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Benzenoid
Monocyclic benzene moiety
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Polyol
Acetal
Ether
Hydrocarbon derivative
Alcohol
Organooxygen compound
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Exogenous (HMDB: HMDB0301937)

Food

Fruit

Berry

Lingonberry (FooDB: FOOD00194)

Process

Not Available

Role

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	0.41 g/L	ALOGPS
logP	4.19	ALOGPS
logP	6.23	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	8.58	ChemAxon
pKa (Strongest Basic)	-5.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	24	ChemAxon
Hydrogen Donor Count	19	ChemAxon
Polar Surface Area	430.52 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	289.21 m³·mol⁻¹	ChemAxon
Polarizability	112.61 Å³	ChemAxon
Number of Rings	13	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB001646

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

Showing chemical card for Epicatechin-(2beta->7,4beta->8)-[epicatechin-(4beta->8)]2-catechin (CFc000281453)

MOL for CFc000281453 (Epicatechin-(2beta->7,4beta->8)-[epicatechin-(4beta->8)]2-catechin)

3D MOL for CFc000281453 (Epicatechin-(2beta->7,4beta->8)-[epicatechin-(4beta->8)]2-catechin)

3D SDF for CFc000281453 (Epicatechin-(2beta->7,4beta->8)-[epicatechin-(4beta->8)]2-catechin)

3D-SDF for CFc000281453 (Epicatechin-(2beta->7,4beta->8)-[epicatechin-(4beta->8)]2-catechin)

PDB for CFc000281453 (Epicatechin-(2beta->7,4beta->8)-[epicatechin-(4beta->8)]2-catechin)

3D PDB for CFc000281453 (Epicatechin-(2beta->7,4beta->8)-[epicatechin-(4beta->8)]2-catechin)

SMILES for CFc000281453 (Epicatechin-(2beta->7,4beta->8)-[epicatechin-(4beta->8)]2-catechin)

INCHI for CFc000281453 (Epicatechin-(2beta->7,4beta->8)-[epicatechin-(4beta->8)]2-catechin)

Structure for CFc000281453 (Epicatechin-(2beta->7,4beta->8)-[epicatechin-(4beta->8)]2-catechin)

3D Structure for CFc000281453 (Epicatechin-(2beta->7,4beta->8)-[epicatechin-(4beta->8)]2-catechin)