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

Details

Stereochemistry ACHIRAL
Molecular Formula C7H7N3
Molecular Weight 133.1506
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-AMINOBENZIMIDAZOLE

SMILES

NC1=NC2=C(N1)C=CC=C2

InChI

InChIKey=JWYUFVNJZUSCSM-UHFFFAOYSA-N
InChI=1S/C7H7N3/c8-7-9-5-3-1-2-4-6(5)10-7/h1-4H,(H3,8,9,10)

HIDE SMILES / InChI

Molecular Formula C7H7N3
Molecular Weight 133.1506
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Potential transition state phosphoramidate inhibitors of beta-tubulin as antifilarial agents.
2001 Jan
Thermodynamic and multinuclear magnetic resonance study of dimethyltin (IV) complexes with some imidazoles in aqueous solutions.
2001 Jan-Feb
On-line automated sample preparation for liquid chromatography using parallel supported liquid membrane extraction and microporous membrane liquid-liquid extraction.
2002 Oct 25
Carbendazim: disposition, cellular permeability, metabolite identification, and pharmacokinetic comparison with its nanoparticle.
2003 Jan
Heterocyclic bis-cations as starting hits for design of inhibitors of the bifunctional enzyme histidine-containing protein kinase/phosphatase from Bacillus subtilis.
2004 Apr 22
Influence of solvent properties on separation and detection performance in non-aqueous capillary electrophoresis-mass spectrometry of basic analytes.
2005 Mar 11
Synthesis of tetrahydrobenzimidazo[1,2-b]quinazolin-1(2H)-one and tetrahydro-1,2,4-triazolo[5,1-b]quinazolin-8(4H)-one ring systems under solvent-free conditions.
2006 Dec
Synthesis and QSAR studies of novel 1-substituted-2-aminobenzimidazoles derivatives.
2006 Sep
Synthesis and biological evaluation of new 3-substituted indole derivatives as potential anti-inflammatory and analgesic agents.
2007 Jun 1
Microwave assisted synthesis of triazoloquinazolinones and benzimidazoquinazolinones.
2007 Mar 5
Synthesis, structure and biological activities of cobalt(II) and zinc(II) coordination compounds with 2-benzimidazole derivatives.
2008 May-Jun
2-Amino-1H-benzoimidazol-3-ium 4,4,4-trifluoro-1,3-dioxo-1-phenyl-butan-2-ide.
2008 Nov 26
Simultaneous analysis of thiabendazole, carbendazim and 2-aminobenzimidazole in concentrated fruit juices by liquid chromatography after a single mix-mode solid-phase extraction cleanup.
2009 Aug
[Characterization of a carbendazim-degrading Trichoderma sp. T2-2 and its application in bioremediation].
2009 Jul
2-Amino-6-nitro-1H-benzoimidazol-3-ium chloride.
2009 Jul 18
One scaffold, three binding modes: novel and selective pteridine reductase 1 inhibitors derived from fragment hits discovered by virtual screening.
2009 Jul 23
2-Aminobenzimidazoles as potent Aurora kinase inhibitors.
2009 Sep 1
Novel small molecule bradykinin B1 receptor antagonists. Part 2: 5-membered diaminoheterocycles.
2010 Feb 1
Concise synthesis of 2, 3-diarylpyrimido[1,2-a]benzimidazole based on isoflavones.
2010 Mar 8
The discovery and structure-activity relationships of 2-(piperidin-3-yl)-1H-benzimidazoles as selective, CNS penetrating H1-antihistamines for insomnia.
2010 May 1
Biodegradation of carbendazim by a novel actinobacterium Rhodococcus jialingiae djl-6-2.
2010 Oct
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:27:50 UTC 2023
Edited
by admin
on Fri Dec 15 17:27:50 UTC 2023
Record UNII
E65DE7521V
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-AMINOBENZIMIDAZOLE
Systematic Name English
AMINOBENZIMIDAZOLE, 2-
Systematic Name English
1H-BENZIMIDAZOL-2-AMINE
Systematic Name English
NSC-7628
Code English
NSC-27793
Code English
Code System Code Type Description
CAS
934-32-7
Created by admin on Fri Dec 15 17:27:50 UTC 2023 , Edited by admin on Fri Dec 15 17:27:50 UTC 2023
PRIMARY
MESH
C027391
Created by admin on Fri Dec 15 17:27:50 UTC 2023 , Edited by admin on Fri Dec 15 17:27:50 UTC 2023
PRIMARY
PUBCHEM
13624
Created by admin on Fri Dec 15 17:27:50 UTC 2023 , Edited by admin on Fri Dec 15 17:27:50 UTC 2023
PRIMARY
NSC
27793
Created by admin on Fri Dec 15 17:27:50 UTC 2023 , Edited by admin on Fri Dec 15 17:27:50 UTC 2023
PRIMARY
CHEBI
27822
Created by admin on Fri Dec 15 17:27:50 UTC 2023 , Edited by admin on Fri Dec 15 17:27:50 UTC 2023
PRIMARY
FDA UNII
E65DE7521V
Created by admin on Fri Dec 15 17:27:50 UTC 2023 , Edited by admin on Fri Dec 15 17:27:50 UTC 2023
PRIMARY
ECHA (EC/EINECS)
213-280-6
Created by admin on Fri Dec 15 17:27:50 UTC 2023 , Edited by admin on Fri Dec 15 17:27:50 UTC 2023
PRIMARY
EPA CompTox
DTXSID1024465
Created by admin on Fri Dec 15 17:27:50 UTC 2023 , Edited by admin on Fri Dec 15 17:27:50 UTC 2023
PRIMARY
NSC
7628
Created by admin on Fri Dec 15 17:27:50 UTC 2023 , Edited by admin on Fri Dec 15 17:27:50 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> METABOLITE