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Details

Stereochemistry ACHIRAL
Molecular Formula C13H10N2
Molecular Weight 194.2319
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-PHENYLBENZIMIDAZOLE

SMILES

N1C2=C(C=CC=C2)N=C1C3=CC=CC=C3

InChI

InChIKey=DWYHDSLIWMUSOO-UHFFFAOYSA-N
InChI=1S/C13H10N2/c1-2-6-10(7-3-1)13-14-11-8-4-5-9-12(11)15-13/h1-9H,(H,14,15)

HIDE SMILES / InChI

Molecular Formula C13H10N2
Molecular Weight 194.2319
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Synthesis, characterization, and biological evaluation of benzimidazole derivatives as potential anxiolytics.
2010-07
Antiviral activity of benzimidazole derivatives. II. Antiviral activity of 2-phenylbenzimidazole derivatives.
2010-04-15
Pharmacophore modeling, resistant mutant isolation, docking, and MM-PBSA analysis: Combined experimental/computer-assisted approaches to identify new inhibitors of the bovine viral diarrhea virus (BVDV).
2010-03-15
1-[6-(9H-Carbazol-9-yl)hex-yl]-2-phenyl-1H-benzimidazole.
2009-11-14
Cytotoxic activity, X-ray crystal structures and spectroscopic characterization of cobalt(II), copper(II) and zinc(II) coordination compounds with 2-substituted benzimidazoles.
2009-09
Synthesis and affinity to DNA of phenylbenzoimidazoles and benzoimidazo[1,2-c]quinazolines.
2009-08
Spectroscopic and calorimetric studies on the DNA recognition of pyrrolo[2,1-c][1,4]benzodiazepine hybrids.
2009-01-15
A solid phase extraction procedure for Fe3+, Cu2+ and Zn2+ ions on 2-phenyl-1H-benzo[d] imidazole loaded on Triton X-100-coated polyvinyl chloride.
2008-10-01
Disruption of Golgi processing by 2-phenyl benzimidazole analogs blocks cell proliferation and slows tumor growth.
2008-05
2-phenylimidazopyridines, a new series of Golgi compounds with potent antiviral activity.
2007-11-29
Light-induced cytotoxicity and genotoxicity of a sunscreen agent, 2-phenylbenzimidazole in Salmonella typhimurium TA 102 and HaCaT keratinocytes.
2007-06
Design, synthesis and utilization of 1- substituted sulphonyloxy-2-phenyl benzimidazole as a novel peptide coupling reagents.
2007
Substituted 2-phenyl-benzimidazole derivatives: novel compounds that suppress key markers of allergy.
2006-08
Prediction of genotoxicity of chemical compounds by statistical learning methods.
2005-06
Novel 2-(substituted phenyl)benzimidazole derivatives with potent activity against IgE, cytokines, and CD23 for the treatment of allergy and asthma.
2004-12-16
Photophysical and photochemical studies of 2-phenylbenzimidazole and UVB sunscreen 2-phenylbenzimidazole-5-sulfonic acid.
2002-02
The interaction of 2-phenylbenzimidazole compounds with DNA: the influence of terminal substituents.
2002
Structural, magnetic and catalytic properties of a self-recognized mu-oxo-bridged diiron(III) bis(benzimidazole) complex.
2001-07-30
[Comparative study of DNA-specific dyes of the indole and benzimidazole derivates].
2001-03-21
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:20:40 GMT 2025
Edited
by admin
on Mon Mar 31 21:20:40 GMT 2025
Record UNII
CB9ZJ140SB
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GAINEX
Preferred Name English
2-PHENYLBENZIMIDAZOLE
Systematic Name English
PHENZIDOLE
Common Name English
N,N'-BENZENYL-O-PHENYLENEDIAMINE
Common Name English
2-PHENYL-1H-BENZIMIDAZOLE [MI]
Common Name English
NSC-251956
Code English
PHENZIDOL
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID5052460
Created by admin on Mon Mar 31 21:20:40 GMT 2025 , Edited by admin on Mon Mar 31 21:20:40 GMT 2025
PRIMARY
CAS
716-79-0
Created by admin on Mon Mar 31 21:20:40 GMT 2025 , Edited by admin on Mon Mar 31 21:20:40 GMT 2025
PRIMARY
ECHA (EC/EINECS)
211-939-2
Created by admin on Mon Mar 31 21:20:40 GMT 2025 , Edited by admin on Mon Mar 31 21:20:40 GMT 2025
PRIMARY
PUBCHEM
12855
Created by admin on Mon Mar 31 21:20:40 GMT 2025 , Edited by admin on Mon Mar 31 21:20:40 GMT 2025
PRIMARY
NSC
251956
Created by admin on Mon Mar 31 21:20:40 GMT 2025 , Edited by admin on Mon Mar 31 21:20:40 GMT 2025
PRIMARY
MERCK INDEX
m8657
Created by admin on Mon Mar 31 21:20:40 GMT 2025 , Edited by admin on Mon Mar 31 21:20:40 GMT 2025
PRIMARY Merck Index
MESH
C117755
Created by admin on Mon Mar 31 21:20:40 GMT 2025 , Edited by admin on Mon Mar 31 21:20:40 GMT 2025
PRIMARY
FDA UNII
CB9ZJ140SB
Created by admin on Mon Mar 31 21:20:40 GMT 2025 , Edited by admin on Mon Mar 31 21:20:40 GMT 2025
PRIMARY