The therapeutic journey of benzimidazoles: A review

Y Bansal, O Silakari - Bioorganic & medicinal chemistry, 2012 - Elsevier
Presence of benzimidazole nucleus in numerous categories of therapeutic agents such as
antimicrobials, antivirals, antiparasites, anticancer, anti-inflammatory, antioxidants, proton …

Benzimidazole-biologically attractive scaffold for protein kinase inhibitors

P Singla, V Luxami, K Paul - RSC Advances, 2014 - pubs.rsc.org
Great advances in elucidating molecular structures allow the precise determination of the
interactions between a protein and a therapeutic agent. Enzyme inhibitors are used as a …

Design, synthesis, molecular docking and cytotoxic evaluation of novel 2-furybenzimidazoles as VEGFR-2 inhibitors

MA Abdullaziz, HT Abdel-Mohsen… - European journal of …, 2017 - Elsevier
Inhibition of angiogenesis through inhibition of vascular endothelial growth factor receptor 2
(VEGFR-2) has been applied in cancer therapy because of its important role in promoting …

Unfolded protein response in cancer: IRE1α inhibition by selective kinase ligands does not impair tumor cell viability

PE Harrington, K Biswas, D Malwitz… - ACS medicinal …, 2015 - ACS Publications
The kinase/endonuclease inositol requiring enzyme 1 (IRE1α), one of the sensors of
unfolded protein accumulation in the endoplasmic reticulum that triggers the unfolded …

[HTML][HTML] Catalyst-controlled chemoselective arylation of 2-aminobenzimidazoles

S Ueda, SL Buchwald - Angewandte Chemie (International ed. in …, 2012 - ncbi.nlm.nih.gov
The chemoselective and complementary Pd-and Cu-catalyzed N-arylation of 2-
aminobenzimidazoles is described. Selective N-arylation of the amino-group was achieved …

Synthesis, cytotoxic evaluation, apoptosis, cell cycle, and molecular docking studies of some new 5-(arylidene/heteroarylidene)-2-(morpholinoimino)-3 …

MA Assiri, TE Ali, MN Alqahtani, AA Shati… - Synthetic …, 2023 - Taylor & Francis
A series of new 5-(arylidene/heteroarylidene)-2-(morpholinoimino)-3-phenylthiazolidin-4-
ones (3–30) was synthesized. Cytotoxic effectiveness of these products was done against …

Novel VEGFR-2 kinase inhibitors identified by the back-to-front approach

K Sanphanya, SK Wattanapitayakul, S Phowichit… - Bioorganic & medicinal …, 2013 - Elsevier
We report a novel VEGFR-2 inhibitor, developed by the back-to-front approach. Docking
experiments indicated that the 3-chloromethylphenylurea motif of the lead compound …

Nickel-catalyzed Chan–Lam cross-coupling: chemoselective N-arylation of 2-aminobenzimidazoles

KA Kumar, P Kannaboina, DN Rao… - Organic & Biomolecular …, 2016 - pubs.rsc.org
A complementary set of Ni-and Cu-based catalyst systems for the selective N-arylation of 2-
aminobenzimidazoles have been developed. Selective N-arylation of the primary amine (C …

Copper‐Catalyzed CNH2 Arylation of 2‐Aminobenzimidazoles and Related C‐Amino‐NH‐azoles

DN Rao, S Rasheed, KA Kumar… - … Synthesis & Catalysis, 2016 - Wiley Online Library
A copper (II)‐catalyzed selective C NH2 arylation of 2‐aminobenzimidazoles and related C‐
amino‐NH‐azoles was achieved in presence of 2, 2′‐bipyridine and cesium carbonate at …

Design, synthesis and anticancer activity of benzofuran derivatives targeting VEGFR-2 tyrosine kinase

OM Abdelhafez, KM Amin, HI Ali, MM Abdalla… - RSC Advances, 2014 - pubs.rsc.org
Two series of chalcone and thiopyrimidine benzofuran derivatives were designed,
synthesized and evaluated in vitro for their vascular endothelial growth factor receptor …