Preferential Synthesis and Pharmacological Evaluation of Mono‐ and Di‐substituted Benzimidazole Derivatives
Author:
Affiliation:
1. Department of Clinical Pharmacy and Pharmacology Faculty of Pharmacy University of Dhaka Dhaka 1000 Bangladesh
Funder
University of Dhaka
Publisher
Wiley
Subject
General Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/slct.202201710
Reference62 articles.
1. Isolation and Properties of Crystalline Cobamide Coenzymes Containing Benzimidazole or 5,6-Dimethylbenzimidazole
2. Design, syntheses, and structure–activity relationships of novel NPY Y5 receptor antagonists: 2-{3-Oxospiro[isobenzofuran-1(3H),4′-piperidin]-1′-yl}benzimidazole derivatives
3. Angiotensin II – AT1 receptor antagonists: Design, synthesis and evaluation of substituted carboxamido benzimidazole derivatives
4. Synthesis and SAR of novel, potent and orally bioavailable benzimidazole inhibitors of poly(ADP-ribose) polymerase (PARP) with a quaternary methylene-amino substituent
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