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

Details

Stereochemistry ACHIRAL
Molecular Formula C11H8O3
Molecular Weight 188.1794
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-HYDROXY-1-NAPHTHOIC ACID

SMILES

OC(=O)C1=C2C=CC=CC2=CC=C1O

InChI

InChIKey=UPHOPMSGKZNELG-UHFFFAOYSA-N
InChI=1S/C11H8O3/c12-9-6-5-7-3-1-2-4-8(7)10(9)11(13)14/h1-6,12H,(H,13,14)

HIDE SMILES / InChI

Molecular Formula C11H8O3
Molecular Weight 188.1794
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Degradation of phenanthrene via meta-cleavage of 2-hydroxy-1-naphthoic acid by Ochrobactrum sp. strain PWTJD.
2010-12
3-(2,4,6-Trimethyl-benzo-yl)-2-naphthoic acid.
2010-10-13
Biodegradation of phenanthrene by Alcaligenes sp. strain PPH: partial purification and characterization of 1-hydroxy-2-naphthoic acid hydroxylase.
2010-10
Long acting beta2-agonist and corticosteroid restore airway glandular cell function altered by bacterial supernatant.
2010-01-20
Rapid degradation of phenanthrene by using Sphingomonas sp. GY2B immobilized in calcium alginate gel beads.
2009-09
Hydroxynaphthoic acid isomer sorption onto goethite.
2009-05-01
Structure of mesh phases in cationic surfactant systems with strongly bound counterions: influence of the surfactant headgroup and the counterion.
2009-03-03
Persistence of birefringence in sheared solutions of wormlike micelles.
2009-01-06
Bacterial degradation of aromatic compounds.
2009-01
Transport evaluation of salicylic acid and structurally related compounds across Caco-2 cell monolayers and artificial PAMPA membranes.
2008-10
Piperidinium 3-hydr-oxy-2-naphthoate.
2008-08-13
Differential developmental toxicity of naphthoic acid isomers in medaka (Oryzias latipes) embryos.
2008
A novel degradation pathway in the assimilation of phenanthrene by Staphylococcus sp. strain PN/Y via meta-cleavage of 2-hydroxy-1-naphthoic acid: formation of trans-2,3-dioxo-5-(2'-hydroxyphenyl)-pent-4-enoic acid.
2007-07
Degradation of phenanthrene by Burkholderia sp. C3: initial 1,2- and 3,4-dioxygenation and meta- and ortho-cleavage of naphthalene-1,2-diol.
2007-02
Synthesis and cytotoxic activity of benzo[a]pyrano[3,2-h] and [2,3-i]xanthone analogues of psorospermine, acronycine, and benzo[a]acronycine.
2006-08
Degradation pathways of phenanthrene by Sinorhizobium sp. C4.
2006-08
Viscosity increase with temperature in cationic surfactant solutions due to the growth of wormlike micelles.
2005-11-22
A novel viscoelastic system from a cationic surfactant and a hydrophobic counterion.
2005-08-15
Chemical synthesis and cytotoxicity of dihydroxylated cyclopentenone analogues of neocarzinostatin chromophore.
2003-06-16
Chemical inactivation of the cinnamate 4-hydroxylase allows for the accumulation of salicylic acid in elicited cells.
2002-10
Inhibitory effect of quinolone antimicrobial and nonsteroidal anti-inflammatory drugs on a medium chain acyl-CoA synthetase.
2001-08-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:08:36 GMT 2025
Edited
by admin
on Mon Mar 31 19:08:36 GMT 2025
Record UNII
E3H4QZ94UY
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-HYDROXY-1-NAPHTHOIC ACID
Systematic Name English
NSC-2803
Preferred Name English
1-NAPHTHALENECARBOXYLIC ACID, 2-HYDROXY-
Common Name English
1-NAPHTHOIC ACID, 2-HYDROXY-
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID9062304
Created by admin on Mon Mar 31 19:08:36 GMT 2025 , Edited by admin on Mon Mar 31 19:08:36 GMT 2025
PRIMARY
FDA UNII
E3H4QZ94UY
Created by admin on Mon Mar 31 19:08:36 GMT 2025 , Edited by admin on Mon Mar 31 19:08:36 GMT 2025
PRIMARY
CAS
2283-08-1
Created by admin on Mon Mar 31 19:08:36 GMT 2025 , Edited by admin on Mon Mar 31 19:08:36 GMT 2025
PRIMARY
NSC
2803
Created by admin on Mon Mar 31 19:08:36 GMT 2025 , Edited by admin on Mon Mar 31 19:08:36 GMT 2025
PRIMARY
ECHA (EC/EINECS)
218-919-2
Created by admin on Mon Mar 31 19:08:36 GMT 2025 , Edited by admin on Mon Mar 31 19:08:36 GMT 2025
PRIMARY
PUBCHEM
16790
Created by admin on Mon Mar 31 19:08:36 GMT 2025 , Edited by admin on Mon Mar 31 19:08:36 GMT 2025
PRIMARY