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2-hydroxybenzylbenzimidazole

Known as: alpha-phenyl-1H-benzimidazole-2-methanol 
National Institutes of Health

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Broader (1)

Benzimidazoles

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Discovery of novel Bcr-AblT315I inhibitors with flexible linker. Part 1: Confirmation optimization of phenyl-1H-indazol-3-amine as hinge binding moiety.
2017
2017
Synthesis of New Thiazolyl Coupled Pyrazoles Bearing 2,4-Thiazolidinedionyl Pharmacophore and Their Anti-Inflammatory and Antibacterial Evaluation.
BACKGROUND 2, 4-Thiazolidinedione (TZD), pyrazole and thiazole heterocyclic rings exhibit a wide range of pharmacological… 
2016
2016
Synthesis and anti-microbial activity of novel series of N-(substituted phenyl-1H-tetrazol-1-yl)-7-substituted tetrazolo [1,5-a]quinoxalin-4yl-aminederivatives
In recent years, tetrazoles fused with quinoxaline ring have been grabbing the attention of the synthetic chemists for their… 
2014
2014
Molecular docking of 1H-pyrazole derivatives to receptor tyrosine kinase and protein kinase for screening potential inhibitors
Tyrosine kinase receptor and protein kinases drawn much attention for the scientific fraternity in drug discovery due to its… 
2012
2012
Synthesis, Characterization and anti -HIV Activity of 4-hydroxy-3-(5-methyl-1- phenyl-1H-pyrazol-3-yl)pyrano(3,2-c)chromene-2,5-dione
8797 A B ST R A C T Substituted 4-hydroxy -2H,5H pyrano (3,2-C) chromene - 2,5 - dione (I) have been prepared by 4-Hydroxy… 
2011
2011
SYNTHESIS OF SOME NOVEL 1-H PYRAZOLE DERIVATIVES AND THEIR ANTIBACTERIAL ACTIVITY STUDIES
When one biologically active molecule is linked to another, the resultant molecule generally has increased potency. Hence two… 
2010
2010
Carbonic anhydrase inhibitors. The beta-carbonic anhydrases from the fungal pathogens Cryptococcus neoformans and Candida albicans are strongly inhibited by substituted-phenyl-1H-indole-5…
Review
2010
Review
2010
3-phenyl-1H-indole-5-sulfonamides: structure-based drug design of a promising class of carbonic anhydrase inhibitors.
A series of 2-(hydrazinocarbonyl)-3-substituted-phenyl-1H-indole-5-sulfonamides possessing various 2-, 3- or 4- substituted… 
2008
2008
Discovery and structure-activity relationship of N-phenyl-1H-pyrazolo[3,4-b]quinolin-4-amines as a new series of potent apoptosis inducers.
1994
1994
Tyrosine kinase inhibitors. 3. Structure-activity relationships for inhibition of protein tyrosine kinases by nuclear-substituted derivatives of 2,2'-dithiobis(1-methyl-N-phenyl-1H-indole-3…
A series of indole-substituted 2,2'-dithiobis(1-methyl-N-phenyl-1H-indole-3-carboxamides) were prepared and evaluated for their… 
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