GOSSYPIN

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C21H20O13
Molecular Weight	480.3757
Optical Activity	UNSPECIFIED
Defined Stereocenters	5 / 5
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

OC[C@H]1O[C@@H](OC2=C3OC(=C(O)C(=O)C3=C(O)C=C2O)C4=CC=C(O)C(O)=C4)[C@H](O)[C@@H](O)[C@@H]1O

InChI

InChIKey=SJRXVLUZMMDCNG-KKPQBLLMSA-N

InChI=1S/C21H20O13/c22-5-11-13(27)15(29)17(31)21(32-11)34-19-10(26)4-9(25)12-14(28)16(30)18(33-20(12)19)6-1-2-7(23)8(24)3-6/h1-4,11,13,15,17,21-27,29-31H,5H2/t11-,13-,15+,17-,21+/m1/s1

HIDE SMILES / InChI

Molecular Formula	C21H20O13
Molecular Weight	480.3757
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	5 / 5
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

PubMed

Title	Date	PubMed
Inhibitory activity of flavonoids and tannins against HIV-1 protease.	2000-09	10993207
Application of the electrotopological state index to QSAR analysis of flavone derivatives as HIV-1 integrase inhibitors.	1996-12	8987091
Inhibition of HIV activation in latently infected cells by flavonoid compounds.	1996-01-01	8825617
Inhibition of HIV-1 integrase by flavones, caffeic acid phenethyl ester (CAPE) and related compounds.	1994-08-03	7520698

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 19:58:17 GMT 2025` Edited by `admin` on `Mon Mar 31 19:58:17 GMT 2025`
Record UNII	A3Q367XWX9
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

GOSSYPIN

Common Name

English

NSC-656276

Preferred Name

English

3,3',4',5,7,8-HEXAHYDROXYFLAVONE 8-GLUCOSIDE

Common Name

English

Code System Code Type Description

PUBCHEM

5281621