| 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 | 172 | 2021 |
| Syntheses of new 3-thiazolyl coumarin derivatives, in vitro α-glucosidase inhibitory activity, and molecular modeling studies U Salar, M Taha, KM Khan, NH Ismail, S Imran, S Perveen, S Gul, ... European journal of medicinal chemistry 122, 196-204, 2016 | 97 | 2016 |
| Synthesis, α-glucosidase inhibitory activity and in silico study of tris-indole hybrid scaffold with oxadiazole ring: As potential leads for the management of type-II diabetes … M Taha, F Rahim, S Imran, NH Ismail, H Ullah, M Selvaraj, MT Javid, ... Bioorganic chemistry 74, 30-40, 2017 | 96 | 2017 |
| Synthesis of benzotriazoles derivatives and their dual potential as α-amylase and α-glucosidase inhibitors in vitro: Structure-activity relationship, molecular docking, and … S Hameed, F Seraj, R Rafique, S Chigurupati, A Wadood, AU Rehman, ... European Journal of Medicinal Chemistry 183, 111677, 2019 | 95 | 2019 |
| New Hybrid Hydrazinyl Thiazole Substituted Chromones: As Potential α-Amylase Inhibitors and Radical (DPPH & ABTS) Scavengers U Salar, KM Khan, S Chigurupati, M Taha, A Wadood, S Vijayabalan, ... Scientific Reports 7, 16980, 2017 | 94 | 2017 |
| 5-Bromo-2-Aryl benzimidazole Derivatives as Non-Cytotoxic Potential Dual Inhibitors of α-Glucosidase and Urease Enzymes T Arshad, KM Khan, N Rasool, U Salar, S Hussain, H Asghar, M Ashraf, ... Bioorganic Chemistry 72, 21-31, 2017 | 88 | 2017 |
| Biology-oriented drug synthesis (BIODS) of 2-(2-methyl-5-nitro-1H-imidazol-1-yl) ethyl aryl ether derivatives, in vitro α-amylase inhibitory activity and in silico studies M Taha, S Imran, NH Ismail, M Selvaraj, F Rahim, S Chigurupati, H Ullah, ... Bioorganic chemistry 74, 1-9, 2017 | 84 | 2017 |
| Hydrazinyl arylthiazole based pyridine scaffolds: Synthesis, structural characterization, in vitro α-glucosidase inhibitory activity, and in silico studies F Ali, KM Khan, U Salar, M Taha, NH Ismail, A Wadood, M Riaz, ... European Journal of Medicinal Chemistry 138, 255-272, 2017 | 78 | 2017 |
| New indole based hybrid oxadiazole scaffolds with N-substituted acetamides: As potent anti-diabetic agents M Nazir, MA Abbasi, SZ Siddiqui, KM Khan, U Salar, M Shahid, M Ashraf, ... Bioorganic chemistry 81, 253-263, 2018 | 74 | 2018 |
| Synthesis, β-glucuronidase inhibition and molecular docking studies of hybrid bisindole-thiosemicarbazides analogs M Taha, NH Ismail, S Imran, F Rahim, A Wadood, H Khan, H Ullah, ... Bioorganic Chemistry 68, 56-63, 2016 | 68 | 2016 |
| 2-Arylquinazolin-4 (3H)-ones: A new class of α-glucosidase inhibitors K Javaid, SM Saad, S Rasheed, ST Moin, N Syed, I Fatima, U Salar, ... Bioorganic & Medicinal Chemistry 23 (23), 7417-7421, 2015 | 66 | 2015 |
| 2ʹ-Aryl and 4ʹ-arylidene substituted pyrazolones: As potential α-amylase inhibitors S Yousuf, KM Khan, U Salar, S Chigurupati, MT Muhammad, A Wadood, ... European journal of medicinal chemistry 159, 47-58, 2018 | 65 | 2018 |
| Flurbiprofen derivatives as novel α-amylase inhibitors: Biology-oriented drug synthesis (BIODS), in vitro, and in silico evaluation M Khan, A Alam, KM Khan, U Salar, S Chigurupati, A Wadood, F Ali, ... Bioorganic chemistry 81, 157-167, 2018 | 64 | 2018 |
| 2-Aryl benzimidazoles: Synthesis, In vitro α-amylase inhibitory activity, and molecular docking study AA Adegboye, KM Khan, U Salar, SA Aboaba, S Chigurupati, I Fatima, ... European Journal of Medicinal Chemistry 150, 248-260, 2018 | 61 | 2018 |
| Synthesis of 6-chloro-2-Aryl-1H-imidazo [4, 5-b] pyridine derivatives: antidiabetic, antioxidant, β-glucuronidase inhibiton and their molecular docking studies M Taha, NH Ismail, S Imran, H Rashwan, W Jamil, S Ali, SM Kashif, ... Bioorganic chemistry 65, 48-56, 2016 | 59 | 2016 |
| Chalcones and Bis-Chalcones: As Potential α-Amylase Inhibitors; Synthesis, In Vitro Screening, and Molecular Modelling Studies AT Bale, KM Khan, U Salar, S Chigurupati, T Fasina, F Ali, A Wadood, ... Bioorganic chemistry 79, 179-189, 2018 | 58 | 2018 |
| 5-Acetyl-6-methyl-4-aryl-3, 4-dihydropyrimidin-2 (1H)-ones: As Potent Urease Inhibitors; Synthesis, In Vitro Screening, and Molecular Modeling Study S Shamim, KM Khan, U Salar, F Ali, MA Lodhi, M Taha, FA Khan, S Ashraf, ... Bioorganic Chemistry 76, 37-52, 2018 | 58 | 2018 |
| Synthesis, in vitro α-glucosidase inhibitory activity and molecular docking studies of new thiazole derivatives KM Khan, S Qurban, U Salar, M Taha, S Hussain, S Perveen, A Hameed, ... Bioorganic chemistry 68, 245-258, 2016 | 58 | 2016 |
| Dihydropyrimidones: as novel class of β-glucuronidase inhibitors F Ali, KM Khan, U Salar, S Iqbal, M Taha, NH Ismail, S Perveen, ... Bioorganic & Medicinal Chemistry 24 (16), 3624-3635, 2016 | 55 | 2016 |
| Synthesis, in vitro α-amylase inhibitory, and radicals (DPPH & ABTS) scavenging potentials of new N-sulfonohydrazide substituted indazoles R Rafique, KM Khan, S Chigurupati, A Wadood, AU Rehman, U Salar, ... Bioorganic Chemistry 94, 103410, 2020 | 54 | 2020 |
Khalid Mohammed KhanH. E. J. Research Institute of Chemistry, University of Karachi, Pakistaniccs.edu의 이메일 확인됨
