| Isatin-derived antibacterial and antifungal compounds and their transition metal complexes ZH Chohan, H Pervez, A Rauf, KM Khan, CT Supuran Journal of Enzyme Inhibition and Medicinal Chemistry 19 (5), 417-423, 2004 | 329 | 2004 |
| Schiff bases in medicinal chemistry: a patent review (2010-2015) A Hameed, M Al-Rashida, M Uroos, S Abid Ali, KM Khan Expert opinion on therapeutic patents 27 (1), 63-79, 2017 | 325 | 2017 |
| Biscoumarin: new class of urease inhibitors; economical synthesis and activity KM Khan, S Iqbal, MA Lodhi, GM Maharvi, MI Choudhary, S Perveen Bioorganic & medicinal chemistry 12 (8), 1963-1968, 2004 | 246 | 2004 |
| Synthesis of bis-Schiff bases of isatins and their antiglycation activity KM Khan, M Khan, M Ali, M Taha, S Rasheed, S Perveen, MI Choudhary Bioorganic & medicinal chemistry 17 (22), 7795-7801, 2009 | 205 | 2009 |
| Structure–activity relationships of tyrosinase inhibitory combinatorial library of 2, 5-disubstituted-1, 3, 4-oxadiazole analogues MTH Khan, MI Choudhary, KM Khan, M Rani Bioorganic & medicinal chemistry 13 (10), 3385-3395, 2005 | 201 | 2005 |
| Quinazoline and quinazolinone as important medicinal scaffolds: a comparative patent review (2011–2016) A Hameed, M Al-Rashida, M Uroos, SA Ali, Arshia, M Ishtiaq, KM Khan Expert opinion on therapeutic patents 28 (4), 281-297, 2018 | 197 | 2018 |
| In-vitro antibacterial, antifungal and cytotoxic properties of sulfonamide—derived Schiff's bases and their metal complexes ZH Chohan, Mahmood-ul-Hassan, KM Khan, CT Supuran Journal of Enzyme Inhibition and Medicinal Chemistry 20 (2), 183-188, 2005 | 189 | 2005 |
| Isatin based Schiff bases as inhibitors of α-glucosidase: Synthesis, characterization, in vitro evaluation and molecular docking studies F Rahim, F Malik, H Ullah, A Wadood, F Khan, MT Javid, M Taha, ... Bioorganic chemistry 60, 42-48, 2015 | 175 | 2015 |
| Synthesis and molecular docking studies of potent α-glucosidase inhibitors based on biscoumarin skeleton KM Khan, F Rahim, A Wadood, N Kosar, M Taha, S Lalani, A Khan, ... European journal of medicinal chemistry 81, 245-252, 2014 | 174 | 2014 |
| Kinetics of novel competitive inhibitors of urease enzymes by a focused library of oxadiazoles/thiadiazoles and triazoles Z Amtul, M Rasheed, MI Choudhary, S Rosanna, KM Khan Biochemical and biophysical research communications 319 (3), 1053-1063, 2004 | 161 | 2004 |
| Synthesis of novel inhibitors of α-glucosidase based on the benzothiazole skeleton containing benzohydrazide moiety and their molecular docking studies M Taha, NH Ismail, S Lalani, MQ Fatmi, S Siddiqui, KM Khan, S Imran, ... European journal of medicinal chemistry 92, 387-400, 2015 | 159 | 2015 |
| Tetraketones: A new class of tyrosinase inhibitors KM Khan, GM Maharvi, MTH Khan, AJ Shaikh, S Perveen, S Begum, ... Bioorganic & medicinal chemistry 14 (2), 344-351, 2006 | 157 | 2006 |
| Multicomponent reactions (MCR) in medicinal chemistry: a patent review (2010-2020) HA Younus, M Al-Rashida, A Hameed, M Uroos, U Salar, S Rana, ... Expert Opinion on Therapeutic Patents 31 (3), 267-289, 2021 | 146 | 2021 |
| Determination of free phenolic acids and antioxidant activity of methanolic extracts obtained from fruits and leaves of Chenopodium album AH Laghari, S Memon, A Nelofar, KM Khan, A Yasmin Food chemistry 126 (4), 1850-1855, 2011 | 144 | 2011 |
| N-Alkylation of anilines, carboxamides and several nitrogen heterocycles using CsF–Celite/alkyl halides/CH3CN combination S Hayat, MI Choudhary, KM Khan, W Schumann, E Bayer Tetrahedron 57 (50), 9951-9957, 2001 | 138 | 2001 |
| Oxazolones: new tyrosinase inhibitors; synthesis and their structure–activity relationships KM Khan, UR Mughal, MTH Khan, S Perveen, MI Choudhary Bioorganic & medicinal chemistry 14 (17), 6027-6033, 2006 | 137 | 2006 |
| Synthesis, molecular docking, acetylcholinesterase and butyrylcholinesterase inhibitory potential of thiazole analogs as new inhibitors for Alzheimer disease F Rahim, MT Javed, H Ullah, A Wadood, M Taha, M Ashraf, MA Khan, ... Bioorganic Chemistry 62, 106-116, 2015 | 136 | 2015 |
| Triazinoindole analogs as potent inhibitors of α-glucosidase: Synthesis, biological evaluation and molecular docking studies F Rahim, K Ullah, H Ullah, A Wadood, M Taha, AU Rehman, M Ashraf, ... Bioorganic Chemistry 58, 81-87, 2015 | 136 | 2015 |
| 3-Formylchromones: Potential antiinflammatory agents KM Khan, N Ambreen, UR Mughal, S Jalil, S Perveen, MI Choudhary European journal of medicinal chemistry 45 (9), 4058-4064, 2010 | 136 | 2010 |
| Schiff bases of 3-formylchromone as thymidine phosphorylase inhibitors KM Khan, N Ambreen, S Hussain, S Perveen, MI Choudhary Bioorganic & medicinal chemistry 17 (8), 2983-2988, 2009 | 129 | 2009 |
Muhammad TahaImam Abdulrahman Bin Faisal University (Formely University of Dammam)在 iau.edu.sa 的电子邮件经过验证
