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
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
Molecular Formula | C9H9N |
Molecular Weight | 131.1745 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
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The oxidation of indole derivatives catalyzed by horseradish peroxidase is highly chemiluminescent. | 2001 Mar 15 |
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Relationship between structures of substituted indolic compounds and their degradation by marine anaerobic microorganisms. | 2002 |
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DNA mediated charge transport: characterization of a DNA radical localized at an artificial nucleic acid base. | 2002 Aug 7 |
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Nature of non-radiative processes involved in the excited state of 9-cyanoanthracene in presence of 2-methylindole/2-methylindoline quenchers. A laser flash photolysis study to reveal the medium effects. | 2002 Jun |
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Novel reversible indole-3-carboxylate decarboxylase catalyzing nonoxidative decarboxylation. | 2002 Nov |
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HPLC of tryptophan and its metabolites: as OPA derivatives and on the basis of their UV and fluorescence spectra, simultaneously. | 2003 |
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Rapid radical formation by DNA charge transport through sequences lacking intervening guanines. | 2003 Jun 4 |
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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 |
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Primary electron-transfer dynamics in 2-phenylindole-9-cyanoanthracene system. A comparative study with 2-methylindole. | 2004 Jul |
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Spirobipyridopyrans, spirobinaphthopyrans, indolinospiropyridopyrans, indolinospironaphthopyrans and indolinospironaphtho-1,4-oxazines: synthesis, study of X-ray crystal structure, antitumoral and antiviral evaluation. | 2004 Mar 1 |
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Adsorption of indole and 2-methylindole on ligand-exchange matrix. | 2004 Oct 1 |
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Indole ring oxidation by activated leukocytes prevents the production of hypochlorous acid. | 2005 Nov |
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CH/pi interactions involving aromatic amino acids: refinement of the CHARMM tryptophan force field. | 2005 Nov 15 |
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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 |
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Functional characterization of two melanocortin (MC) receptors in lamprey showing orthology to the MC1 and MC4 receptor subtypes. | 2007 Jun 29 |
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Indolequinone antitumour agents: correlation between quinone structure and rate of metabolism by recombinant human NAD(P)H:quinone oxidoreductase. | 2007 May 21 |
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Sub-parts per billion detection of trace volatile chemicals in human breath using selected ion flow tube mass spectrometry. | 2008 Jul 10 |
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Synthesis and pharmacological evaluation of peptide-mimetic protease-activated receptor-1 antagonists containing novel heterocyclic scaffolds. | 2008 Jun 1 |
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Synthesis and cytotoxicity studies of new morpholino-functionalised and N-heteroaryl-substituted titanocene anticancer drugs. | 2008 Mar |
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Novel multicomponent reactions involving isoquinoline or phenanthridine and activated acetylenic ester in the presence of heterocyclic NH or 1,3-dicarbonyl compounds. | 2008 May |
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An odorant receptor from the southern house mosquito Culex pipiens quinquefasciatus sensitive to oviposition attractants. | 2010 Apr 8 |
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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 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:38:03 GMT 2023
by
admin
on
Fri Dec 15 18:38:03 GMT 2023
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Record UNII |
I7CN58827I
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Record Status |
Validated (UNII)
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Record Version |
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2-METHYLINDOLE
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95-20-5
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DTXSID5059117
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49402
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7224
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I7CN58827I
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202-398-3
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7514
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