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Bioorganic Chemistry|December 4, 2020
Synthesis of azachalcones, their α-amylase, α-glucosidase inhibitory activities, kinetics, and molecular docking studiesFaiza Saleem, Kanwal, Khalid Mohammed Khan, et al.Molecular Diversity|March 2, 2021
Dihydroquinazolin-4(1H)-one derivatives as novel and potential leads for diabetic managementOluwatoyin Babatunde, Shehryar Hameed, Uzma Salar, et al.Chemical & Pharmaceutical Bulletin|January 7, 2005
Synthesis and pharmacological activity of 4-(4'-(chlorophenyl)-4-hydroxypiperidine) derivativesZafar Saeed Saify, Nousheen Mushtaq, Khalid Mohammed Khan, et al.Natural Product Research|July 13, 2006
Piperidines: a new class of urease inhibitorsKhalid Mohammed Khan, Zafar S Saify, Muhammad Arif Lodhi, et al.Bioorganic Chemistry|November 5, 2018
Schiff bases of tryptamine as potent inhibitors of nucleoside triphosphate diphosphohydrolases (NTPDases): Structure-activity relationshipKanwal, Khalid Mohammed Khan, Uzma Salar, et al.Journal of Molecular Graphics & Modelling|August 6, 2011
Molecular modeling-based antioxidant arylidene barbiturates as urease inhibitorsKhalid Mohammed Khan, Muhammad Ali, Abdul Wadood, et al.Journal of Molecular Graphics & Modelling|March 27, 2010
Identification of potent urease inhibitors via ligand- and structure-based virtual screening and in vitro assaysKhalid M Khan, Abdul Wadood, Muhammad Ali, et al.Bioorganic Chemistry|May 16, 2020
Synthesis, in vitro and in silico screening of 2-amino-4-aryl-6-(phenylthio) pyridine-3,5-dicarbonitriles as novel α-glucosidase inhibitorsMuhammad Ali, Khalid Mohammed Khan, Mohammad Mahdavi, et al.European Journal of Medicinal Chemistry|October 1, 2018
2'-Aryl and 4'-arylidene substituted pyrazolones: As potential α-amylase inhibitorsSahar Yousuf, Khalid Mohammed Khan, Uzma Salar, et al.Bioorganic & Medicinal Chemistry|July 3, 2014
Synthesis and structure-activity relationship of thiobarbituric acid derivatives as potent inhibitors of ureaseKhalid Mohammed Khan, Fazal Rahim, Ajmal Khan, et al.Pageof 16