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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 of GOSSYPIN

SMILES

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

PubMed

TitleDatePubMed
Inhibition of HIV activation in latently infected cells by flavonoid compounds.
1996 Jan 1
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:50:20 GMT 2023
Edited
by admin
on Fri Dec 15 19:50:20 GMT 2023
Record UNII
A3Q367XWX9
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GOSSYPIN
Common Name English
NSC-656276
Code English
3,3',4',5,7,8-HEXAHYDROXYFLAVONE 8-GLUCOSIDE
Common Name English
Code System Code Type Description
PUBCHEM
5281621
Created by admin on Fri Dec 15 19:50:20 GMT 2023 , Edited by admin on Fri Dec 15 19:50:20 GMT 2023
PRIMARY
EPA CompTox
DTXSID60215512
Created by admin on Fri Dec 15 19:50:20 GMT 2023 , Edited by admin on Fri Dec 15 19:50:20 GMT 2023
PRIMARY
NSC
656276
Created by admin on Fri Dec 15 19:50:20 GMT 2023 , Edited by admin on Fri Dec 15 19:50:20 GMT 2023
PRIMARY
CAS
652-78-8
Created by admin on Fri Dec 15 19:50:20 GMT 2023 , Edited by admin on Fri Dec 15 19:50:20 GMT 2023
PRIMARY
FDA UNII
A3Q367XWX9
Created by admin on Fri Dec 15 19:50:20 GMT 2023 , Edited by admin on Fri Dec 15 19:50:20 GMT 2023
PRIMARY