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Details

Stereochemistry ACHIRAL
Molecular Formula C14H11N
Molecular Weight 193.2438
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3-PHENYLINDOLE

SMILES

N1C=C(C2=C1C=CC=C2)C3=CC=CC=C3

InChI

InChIKey=XZNGTBLWFCRXKR-UHFFFAOYSA-N
InChI=1S/C14H11N/c1-2-6-11(7-3-1)13-10-15-14-9-5-4-8-12(13)14/h1-10,15H

HIDE SMILES / InChI

Molecular Formula C14H11N
Molecular Weight 193.2438
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Accurately characterizing the pi-pi interaction energies of indole-benzene complexes.
2010-03-18
Substrate specificity and inhibition of brassinin hydrolases, detoxifying enzymes from the plant pathogens Leptosphaeria maculans and Alternaria brassicicola.
2009-12
Cloning, purification and characterisation of brassinin glucosyltransferase, a phytoalexin-detoxifying enzyme from the plant pathogen Sclerotinia sclerotiorum.
2009-02
Methyl 3-(4-bromo-phen-yl)-2-(1H-indol-3-ylmeth-yl)-5-[1-(4-methoxy-phen-yl)-4-oxo-2-phenyl-azetidin-2-yl]-4-nitro-pyrrolidine-2-carboxyl-ate.
2008-05-17
Design, synthesis, and evaluation of potential inhibitors of brassinin glucosyltransferase, a phytoalexin detoxifying enzyme from Sclerotinia sclerotiorum.
2007-09-01
Camalexin induces detoxification of the phytoalexin brassinin in the plant pathogen Leptosphaeria maculans.
2005-11
Protein engineering of toluene ortho-monooxygenase of Burkholderia cepacia G4 for regiospecific hydroxylation of indole to form various indigoid compounds.
2005-01
Synthesis and antitumor activity of substituted 3-(5-imidazo[2,1-b]thiazolylmethylene)-2-indolinones.
2002-04-19
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 19:02:50 GMT 2025
Edited
by admin
on Mon Mar 31 19:02:50 GMT 2025
Record UNII
7676CPK41G
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3-PHENYLINDOLE
Systematic Name English
NSC-76690
Preferred Name English
Code System Code Type Description
MESH
C037177
Created by admin on Mon Mar 31 19:02:50 GMT 2025 , Edited by admin on Mon Mar 31 19:02:50 GMT 2025
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FDA UNII
7676CPK41G
Created by admin on Mon Mar 31 19:02:50 GMT 2025 , Edited by admin on Mon Mar 31 19:02:50 GMT 2025
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NSC
76690
Created by admin on Mon Mar 31 19:02:50 GMT 2025 , Edited by admin on Mon Mar 31 19:02:50 GMT 2025
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CAS
1504-16-1
Created by admin on Mon Mar 31 19:02:50 GMT 2025 , Edited by admin on Mon Mar 31 19:02:50 GMT 2025
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EPA CompTox
DTXSID80164538
Created by admin on Mon Mar 31 19:02:50 GMT 2025 , Edited by admin on Mon Mar 31 19:02:50 GMT 2025
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PUBCHEM
96502
Created by admin on Mon Mar 31 19:02:50 GMT 2025 , Edited by admin on Mon Mar 31 19:02:50 GMT 2025
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