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

Details

Stereochemistry ACHIRAL
Molecular Formula C9H9N
Molecular Weight 131.1745
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-METHYLINDOLE

SMILES

CC1=CC2=C(N1)C=CC=C2

InChI

InChIKey=BHNHHSOHWZKFOX-UHFFFAOYSA-N
InChI=1S/C9H9N/c1-7-6-8-4-2-3-5-9(8)10-7/h2-6,10H,1H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
DNA mediated charge transport: characterization of a DNA radical localized at an artificial nucleic acid base.
2002 Aug 7
Novel reversible indole-3-carboxylate decarboxylase catalyzing nonoxidative decarboxylation.
2002 Nov
HPLC of tryptophan and its metabolites: as OPA derivatives and on the basis of their UV and fluorescence spectra, simultaneously.
2003
Rapid radical formation by DNA charge transport through sequences lacking intervening guanines.
2003 Jun 4
The reaction of indole with the aminoacrylate intermediate of Salmonella typhimurium tryptophan synthase: observation of a primary kinetic isotope effect with 3-[(2)H]indole.
2004 Dec 15
Primary electron-transfer dynamics in 2-phenylindole-9-cyanoanthracene system. A comparative study with 2-methylindole.
2004 Jul
Spirobipyridopyrans, spirobinaphthopyrans, indolinospiropyridopyrans, indolinospironaphthopyrans and indolinospironaphtho-1,4-oxazines: synthesis, study of X-ray crystal structure, antitumoral and antiviral evaluation.
2004 Mar 1
Adsorption of indole and 2-methylindole on ligand-exchange matrix.
2004 Oct 1
CH/pi interactions involving aromatic amino acids: refinement of the CHARMM tryptophan force field.
2005 Nov 15
Development and validation of a method for simultaneous analysis of the boar taint compounds indole, skatole and androstenone in pig fat using liquid chromatography-multiple mass spectrometry.
2007 Dec 7
Sub-parts per billion detection of trace volatile chemicals in human breath using selected ion flow tube mass spectrometry.
2008 Jul 10
A novel hydroxyfuroic acid compound as an insulin receptor activator. Structure and activity relationship of a prenylindole moiety to insulin receptor activation.
2009 Jul 30
Carbon nucleophilicities of indoles in S(N)Ar substitutions of superelectrophilic 7-chloro-4,6-dinitrobenzofuroxan and -benzofurazan.
2009 May 1
An odorant receptor from the southern house mosquito Culex pipiens quinquefasciatus sensitive to oviposition attractants.
2010 Apr 8
The relevance of the collaborative effect in determining the performances of photorefractive polymer materials.
2010 Feb 1
The Anopheles gambiae odorant binding protein 1 (AgamOBP1) mediates indole recognition in the antennae of female mosquitoes.
2010 Mar 1
Cytosolic action of phytochelatin synthase.
2010 May
Bioactivation of a novel 2-methylindole-containing dual chemoattractant receptor-homologous molecule expressed on T-helper type-2 cells/D-prostanoid receptor antagonist leads to mechanism-based CYP3A inactivation: glutathione adduct characterization and prediction of in vivo drug-drug interaction.
2010 May
Patents
Name Type Language
2-METHYLINDOLE
Systematic Name English
NSC-7514
Code English
2-METHYL-1H-INDOLE
Systematic Name English
INDOLE, 2-METHYL-
Systematic Name English
1H-INDOLE, 2-METHYL-
Systematic Name English
Code System Code Type Description
WIKIPEDIA
2-METHYLINDOLE
Created by admin on Fri Dec 15 18:38:03 GMT 2023 , Edited by admin on Fri Dec 15 18:38:03 GMT 2023
PRIMARY
CAS
95-20-5
Created by admin on Fri Dec 15 18:38:03 GMT 2023 , Edited by admin on Fri Dec 15 18:38:03 GMT 2023
PRIMARY
EPA CompTox
DTXSID5059117
Created by admin on Fri Dec 15 18:38:03 GMT 2023 , Edited by admin on Fri Dec 15 18:38:03 GMT 2023
PRIMARY
CHEBI
49402
Created by admin on Fri Dec 15 18:38:03 GMT 2023 , Edited by admin on Fri Dec 15 18:38:03 GMT 2023
PRIMARY
PUBCHEM
7224
Created by admin on Fri Dec 15 18:38:03 GMT 2023 , Edited by admin on Fri Dec 15 18:38:03 GMT 2023
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FDA UNII
I7CN58827I
Created by admin on Fri Dec 15 18:38:03 GMT 2023 , Edited by admin on Fri Dec 15 18:38:03 GMT 2023
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ECHA (EC/EINECS)
202-398-3
Created by admin on Fri Dec 15 18:38:03 GMT 2023 , Edited by admin on Fri Dec 15 18:38:03 GMT 2023
PRIMARY
NSC
7514
Created by admin on Fri Dec 15 18:38:03 GMT 2023 , Edited by admin on Fri Dec 15 18:38:03 GMT 2023
PRIMARY