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Details

Stereochemistry ACHIRAL
Molecular Formula C7H8O3
Molecular Weight 140.1366
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GENTISYL ALCOHOL

SMILES

OCC1=CC(O)=CC=C1O

InChI

InChIKey=PUZSUVGRVHEUQO-UHFFFAOYSA-N
InChI=1S/C7H8O3/c8-4-5-3-6(9)1-2-7(5)10/h1-3,8-10H,4H2

HIDE SMILES / InChI

Molecular Formula C7H8O3
Molecular Weight 140.1366
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Dual reactivity of hydroxy- and methoxy- substituted o-quinone methides in aqueous solutions: hydration versus tautomerization.
2010-11-05
Biosynthesis and toxicological effects of patulin.
2010-04
Molecular cloning and functional characterization of two CYP619 cytochrome P450s involved in biosynthesis of patulin in Aspergillus clavatus.
2009-05
Gentisyl alcohol derivatives from the marine-derived fungus Penicillium terrestre.
2008-01
Screening for metabolites from Penicillium novae-zeelandiae displaying radical-scavenging activity and oxidative mutagenicity: isolation of gentisyl alcohol.
2003-08-05
Parasitenone, a new epoxycyclohexenone related to gabosine from the marine-derived fungus Aspergillus parasiticus.
2002-05
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:53:37 GMT 2025
Edited
by admin
on Mon Mar 31 19:53:37 GMT 2025
Record UNII
T8T2WY38GH
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GENTISYL ALCOHOL
MI  
Systematic Name English
BE-53594B
Preferred Name English
GENTISIN ALCOHOL
Common Name English
SALIREPOL
Common Name English
1,4-BENZENEDIOL, 2-(HYDROXYMETHYL)-
Systematic Name English
2,5-DIHYDROXYBENZYL ALCOHOL
Systematic Name English
GENTISYL ALCOHOL [MI]
Common Name English
Code System Code Type Description
MERCK INDEX
m743
Created by admin on Mon Mar 31 19:53:37 GMT 2025 , Edited by admin on Mon Mar 31 19:53:37 GMT 2025
PRIMARY Merck Index
CAS
495-08-9
Created by admin on Mon Mar 31 19:53:37 GMT 2025 , Edited by admin on Mon Mar 31 19:53:37 GMT 2025
PRIMARY
FDA UNII
T8T2WY38GH
Created by admin on Mon Mar 31 19:53:37 GMT 2025 , Edited by admin on Mon Mar 31 19:53:37 GMT 2025
PRIMARY
PUBCHEM
188287
Created by admin on Mon Mar 31 19:53:37 GMT 2025 , Edited by admin on Mon Mar 31 19:53:37 GMT 2025
PRIMARY
CHEBI
5325
Created by admin on Mon Mar 31 19:53:37 GMT 2025 , Edited by admin on Mon Mar 31 19:53:37 GMT 2025
PRIMARY
EPA CompTox
DTXSID60197804
Created by admin on Mon Mar 31 19:53:37 GMT 2025 , Edited by admin on Mon Mar 31 19:53:37 GMT 2025
PRIMARY