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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=CC(O)=CC=C2C1=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 Jul 5
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 09:36:20 UTC 2023
Edited
by admin
on Sat Dec 16 09:36:20 UTC 2023
Record UNII
C308QR79UE
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FUSTIN, (+)-
Common 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
Common 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 Sat Dec 16 09:36:21 UTC 2023 , Edited by admin on Sat Dec 16 09:36:21 UTC 2023
PRIMARY Merck Index
FDA UNII
C308QR79UE
Created by admin on Sat Dec 16 09:36:21 UTC 2023 , Edited by admin on Sat Dec 16 09:36:21 UTC 2023
PRIMARY
CAS
4382-36-9
Created by admin on Sat Dec 16 09:36:21 UTC 2023 , Edited by admin on Sat Dec 16 09:36:21 UTC 2023
PRIMARY
PUBCHEM
5317435
Created by admin on Sat Dec 16 09:36:21 UTC 2023 , Edited by admin on Sat Dec 16 09:36:21 UTC 2023
PRIMARY
Related Record Type Details
RACEMATE -> ENANTIOMER
ENANTIOMER -> ENANTIOMER