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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=CC=CC=C2N=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
Structural, magnetic and catalytic properties of a self-recognized mu-oxo-bridged diiron(III) bis(benzimidazole) complex.
2001 Jul 30
Novel 2-(substituted phenyl)benzimidazole derivatives with potent activity against IgE, cytokines, and CD23 for the treatment of allergy and asthma.
2004 Dec 16
Prediction of genotoxicity of chemical compounds by statistical learning methods.
2005 Jun
Substituted 2-phenyl-benzimidazole derivatives: novel compounds that suppress key markers of allergy.
2006 Aug
Design, synthesis and utilization of 1- substituted sulphonyloxy-2-phenyl benzimidazole as a novel peptide coupling reagents.
2007
Light-induced cytotoxicity and genotoxicity of a sunscreen agent, 2-phenylbenzimidazole in Salmonella typhimurium TA 102 and HaCaT keratinocytes.
2007 Jun
2-phenylimidazopyridines, a new series of Golgi compounds with potent antiviral activity.
2007 Nov 29
Disruption of Golgi processing by 2-phenyl benzimidazole analogs blocks cell proliferation and slows tumor growth.
2008 May
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 Oct 1
Synthesis and affinity to DNA of phenylbenzoimidazoles and benzoimidazo[1,2-c]quinazolines.
2009 Aug
Spectroscopic and calorimetric studies on the DNA recognition of pyrrolo[2,1-c][1,4]benzodiazepine hybrids.
2009 Jan 15
1-[6-(9H-Carbazol-9-yl)hex-yl]-2-phenyl-1H-benzimidazole.
2009 Nov 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 Sep
Antiviral activity of benzimidazole derivatives. II. Antiviral activity of 2-phenylbenzimidazole derivatives.
2010 Apr 15
Synthesis, characterization, and biological evaluation of benzimidazole derivatives as potential anxiolytics.
2010 Jul
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 Mar 15
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 04:02:14 GMT 2023
Edited
by admin
on Sat Dec 16 04:02:14 GMT 2023
Record UNII
CB9ZJ140SB
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-PHENYLBENZIMIDAZOLE
Systematic Name English
PHENZIDOLE
Common Name English
GAINEX
Brand 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 Sat Dec 16 04:02:14 GMT 2023 , Edited by admin on Sat Dec 16 04:02:14 GMT 2023
PRIMARY
CAS
716-79-0
Created by admin on Sat Dec 16 04:02:14 GMT 2023 , Edited by admin on Sat Dec 16 04:02:14 GMT 2023
PRIMARY
ECHA (EC/EINECS)
211-939-2
Created by admin on Sat Dec 16 04:02:14 GMT 2023 , Edited by admin on Sat Dec 16 04:02:14 GMT 2023
PRIMARY
PUBCHEM
12855
Created by admin on Sat Dec 16 04:02:14 GMT 2023 , Edited by admin on Sat Dec 16 04:02:14 GMT 2023
PRIMARY
NSC
251956
Created by admin on Sat Dec 16 04:02:14 GMT 2023 , Edited by admin on Sat Dec 16 04:02:14 GMT 2023
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MERCK INDEX
m8657
Created by admin on Sat Dec 16 04:02:14 GMT 2023 , Edited by admin on Sat Dec 16 04:02:14 GMT 2023
PRIMARY Merck Index
MESH
C117755
Created by admin on Sat Dec 16 04:02:14 GMT 2023 , Edited by admin on Sat Dec 16 04:02:14 GMT 2023
PRIMARY
FDA UNII
CB9ZJ140SB
Created by admin on Sat Dec 16 04:02:14 GMT 2023 , Edited by admin on Sat Dec 16 04:02:14 GMT 2023
PRIMARY