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Details

Stereochemistry ACHIRAL
Molecular Formula C12H10O3
Molecular Weight 202.206
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1-NAPHTHOXYACETIC ACID

SMILES

OC(=O)COC1=CC=CC2=CC=CC=C12

InChI

InChIKey=GHRYSOFWKRRLMI-UHFFFAOYSA-N
InChI=1S/C12H10O3/c13-12(14)8-15-11-7-3-5-9-4-1-2-6-10(9)11/h1-7H,8H2,(H,13,14)

HIDE SMILES / InChI

Molecular Formula C12H10O3
Molecular Weight 202.206
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Analysis of vascular development in the hydra sterol biosynthetic mutants of Arabidopsis.
2010-08-17
Auxin influx inhibitors 1-NOA, 2-NOA, and CHPAA interfere with membrane dynamics in tobacco cells.
2010-08
Expression profile of PIN, AUX/LAX and PGP auxin transporter gene families in Sorghum bicolor under phytohormone and abiotic stress.
2010-07
Synthesis of new 2-naphthyl ethers and their protective activities against DNA damage induced by bleomycin-iron.
2009-12
Auxin redistribution modulates plastic development of root system architecture under salt stress in Arabidopsis thaliana.
2009-10-15
Determination of naphthalene by competitive fluorescence immunoassay.
2009-07
Bis[μ-2-(2-naphth-oxy)acetato]bis-{aqua[2-(2-naphth-oxy)acetato]zinc(II)}.
2009-04-22
Root system architecture from coupling cell shape to auxin transport.
2008-12-16
Ethylene regulates lateral root formation and auxin transport in Arabidopsis thaliana.
2008-07
Functional characterization of PaLAX1, a putative auxin permease, in heterologous plant systems.
2008-03
Identification of auxins by a chemical genomics approach.
2008
Expression of gibberellin 20-oxidase1 (AtGA20ox1) in Arabidopsis seedlings with altered auxin status is regulated at multiple levels.
2008
Auxin influx activity is associated with Frankia infection during actinorhizal nodule formation in Casuarina glauca.
2007-08
2-Amino-2-thiazoline and its 1:1 organic salt with 2-naphthoxyacetic acid.
2004-09
Determination of phytohormones of environmental impact by capillary zone electrophoresis.
2004-03-24
Auxin and ethylene response interactions during Arabidopsis root hair development dissected by auxin influx modulators.
2002-12
Control of propranolol intake by direct chromatographic detection of alpha-naphthoxylactic acid in urine.
2002-02-15
Development of generic liquid chromatography-mass spectrometry methods using experimental design.
2002-01
Toward designed assembly of microporous coordination networks constructed from silver(I)-hexamethylenetetramine layers.
2001-07-02
Novel auxin transport inhibitors phenocopy the auxin influx carrier mutation aux1.
2001-02
Substance Class Chemical
Created
by admin
on Mon Mar 31 23:34:43 GMT 2025
Edited
by admin
on Mon Mar 31 23:34:43 GMT 2025
Record UNII
9QI2464POA
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-9847
Preferred Name English
1-NAPHTHOXYACETIC ACID
Systematic Name English
NAPHTHALENE 1-CARBOXYMETHYL ETHER
Systematic Name English
1-NAPHTHYLOXYACETIC ACID
Systematic Name English
NAPHTHOXYACETIC ACID
Systematic Name English
ACETIC ACID, 2-(1-NAPHTHALENYLOXY)-
Systematic Name English
1-NAPHTHALENYLOXYACETIC ACID
Systematic Name English
2-(1-NAPHTHOXY)ACETIC ACID
Systematic Name English
.ALPHA.-NAPHTHOXYACETIC ACID
Systematic Name English
Code System Code Type Description
CAS
2976-75-2
Created by admin on Mon Mar 31 23:34:43 GMT 2025 , Edited by admin on Mon Mar 31 23:34:43 GMT 2025
PRIMARY
PUBCHEM
76313
Created by admin on Mon Mar 31 23:34:43 GMT 2025 , Edited by admin on Mon Mar 31 23:34:43 GMT 2025
PRIMARY
ECHA (EC/EINECS)
221-023-4
Created by admin on Mon Mar 31 23:34:43 GMT 2025 , Edited by admin on Mon Mar 31 23:34:43 GMT 2025
PRIMARY
EPA CompTox
DTXSID30183911
Created by admin on Mon Mar 31 23:34:43 GMT 2025 , Edited by admin on Mon Mar 31 23:34:43 GMT 2025
PRIMARY
CHEBI
44588
Created by admin on Mon Mar 31 23:34:43 GMT 2025 , Edited by admin on Mon Mar 31 23:34:43 GMT 2025
PRIMARY
FDA UNII
9QI2464POA
Created by admin on Mon Mar 31 23:34:43 GMT 2025 , Edited by admin on Mon Mar 31 23:34:43 GMT 2025
PRIMARY
DRUG BANK
DB08286
Created by admin on Mon Mar 31 23:34:43 GMT 2025 , Edited by admin on Mon Mar 31 23:34:43 GMT 2025
PRIMARY
NSC
9847
Created by admin on Mon Mar 31 23:34:43 GMT 2025 , Edited by admin on Mon Mar 31 23:34:43 GMT 2025
PRIMARY
Related Record Type Details
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