U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C15H12O6
Molecular Weight 288.2522
Optical Activity ( + )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FUSTIN, (+)-

SMILES

O[C@@H]1[C@H](OC2=C(C=CC(O)=C2)C1=O)C3=CC(O)=C(O)C=C3

InChI

InChIKey=FNUPUYFWZXZMIE-LSDHHAIUSA-N
InChI=1S/C15H12O6/c16-8-2-3-9-12(6-8)21-15(14(20)13(9)19)7-1-4-10(17)11(18)5-7/h1-6,14-18,20H/t14-,15+/m0/s1

HIDE SMILES / InChI

Molecular Formula C15H12O6
Molecular Weight 288.2522
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Differential inhibitory effects of various flavonoids on the activities of reverse transcriptase and cellular DNA and RNA polymerases.
1990-07-05
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:45:09 GMT 2025
Edited
by admin
on Mon Mar 31 22:45:09 GMT 2025
Record UNII
C308QR79UE
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FUSTIN, (+)-
Common Name English
(+)-FUSTIN
Preferred Name English
4H-1-BENZOPYRAN-4-ONE, 2-(3,4-DIHYDROXYPHENYL)-2,3-DIHYDRO-3,7-DIHYDROXY-, (2R,3R)-
Systematic Name English
2,3-TRANS-FUSTIN
Common Name English
FLAVANONE, 3,3',4',7-TETRAHYDROXY-, (+)-
Systematic Name English
FUSTIN (2R,3R)-FORM [MI]
Common Name English
(2R,3R)-2-(3,4-DIHYDROXYPHENYL)-2,3-DIHYDRO-3,7-DIHYDROXY-4H-1-BENZOPYRAN-4-ONE
Common Name English
4H-1-BENZOPYRAN-4-ONE, 2-(3,4-DIHYDROXYPHENYL)-2,3-DIHYDRO-3,7-DIHYDROXY-, (2R-TRANS)-
Common Name English
Code System Code Type Description
MERCK INDEX
m5617
Created by admin on Mon Mar 31 22:45:09 GMT 2025 , Edited by admin on Mon Mar 31 22:45:09 GMT 2025
PRIMARY Merck Index
FDA UNII
C308QR79UE
Created by admin on Mon Mar 31 22:45:09 GMT 2025 , Edited by admin on Mon Mar 31 22:45:09 GMT 2025
PRIMARY
CAS
4382-36-9
Created by admin on Mon Mar 31 22:45:09 GMT 2025 , Edited by admin on Mon Mar 31 22:45:09 GMT 2025
PRIMARY
PUBCHEM
5317435
Created by admin on Mon Mar 31 22:45:09 GMT 2025 , Edited by admin on Mon Mar 31 22:45:09 GMT 2025
PRIMARY
EPA CompTox
DTXSID401136309
Created by admin on Mon Mar 31 22:45:09 GMT 2025 , Edited by admin on Mon Mar 31 22:45:09 GMT 2025
PRIMARY
Related Record Type Details
RACEMATE -> ENANTIOMER
ENANTIOMER -> ENANTIOMER