Mohammad Shahar Yar

ORCID: 0000-0001-9298-0154
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About
Contact & Profiles
Research Areas
  • Synthesis and biological activity
  • Synthesis and Biological Evaluation
  • Synthesis and Characterization of Heterocyclic Compounds
  • Click Chemistry and Applications
  • Multicomponent Synthesis of Heterocycles
  • Phenothiazines and Benzothiazines Synthesis and Activities
  • Computational Drug Discovery Methods
  • Quinazolinone synthesis and applications
  • Cholinesterase and Neurodegenerative Diseases
  • Cancer therapeutics and mechanisms
  • Tuberculosis Research and Epidemiology
  • Antimicrobial Peptides and Activities
  • Chemical Synthesis and Analysis
  • Synthesis of heterocyclic compounds
  • Synthesis and Reactions of Organic Compounds
  • Analytical Methods in Pharmaceuticals
  • Bioactive Compounds and Antitumor Agents
  • Alzheimer's disease research and treatments
  • HIV/AIDS drug development and treatment
  • Drug-Induced Hepatotoxicity and Protection
  • Neuroscience and Neuropharmacology Research
  • Diabetes Treatment and Management
  • Peptidase Inhibition and Analysis
  • Drug Transport and Resistance Mechanisms
  • Liver Disease Diagnosis and Treatment

Jamia Hamdard
2016-2025

Hamdard University
2008-2025

Government College University, Faisalabad
2025

Karachi Medical and Dental College
2024

Delhi Pharmaceutical Science and Research University
2019-2024

Jadavpur University
2022

AIMST University
2022

University of Agriculture Faisalabad
2020

COMSATS University Islamabad
2019

Kurukshetra University
2011

Synthesis of commercially available benzimidazole involves condensation o-phenylenediamine with formic acid. The most prominent compound in nature is N-riosyldimethylbenzimidazole, which serves as a axial ligand for cobalt vitamin B12. and its derivatives play very important role therapeutic agent e.g. antiulcer anthelmintic drugs. Apart from this the exhibit pharmacological activities such antimicrobial, antiviral, anticancer, anti-inflammatory, analgesic, etc. substituted benzimidazoles...

10.1016/j.arabjc.2012.07.017 article EN cc-by-nc-nd Arabian Journal of Chemistry 2012-08-03

10.1016/j.bmcl.2007.04.004 article EN Bioorganic & Medicinal Chemistry Letters 2007-04-07
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