| 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 | 178 | 2015 |
| 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 | 142 | 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 | 139 | 2015 |
| Synthesis, in vitro evaluation and molecular docking studies of thiazole derivatives as new inhibitors of α-glucosidase F Rahim, H Ullah, MT Javid, A Wadood, M Taha, M Ashraf, A Shaukat, ... Bioorganic chemistry 62, 15-21, 2015 | 130 | 2015 |
| Synthesis and in vitro acetylcholinesterase and butyrylcholinesterase inhibitory potential of hydrazide based Schiff bases F Rahim, H Ullah, M Taha, A Wadood, MT Javed, W Rehman, M Nawaz, ... Bioorganic Chemistry 68, 30-40, 2016 | 105 | 2016 |
| Synthesis of 4-thiazolidinone analogs as potent in vitro anti-urease agents F Rahim, K Zaman, H Ullah, M Taha, A Wadood, MT Javed, W Rehman, ... Bioorganic chemistry 63, 123-131, 2015 | 102 | 2015 |
| Synthesis and study of the α-amylase inhibitory potential of thiadiazole quinoline derivatives M Taha, MT Javid, S Imran, M Selvaraj, S Chigurupati, H Ullah, F Rahim, ... Bioorganic chemistry 74, 179-186, 2017 | 95 | 2017 |
| 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 | 90 | 2017 |
| Synthesis of alpha amylase inhibitors based on privileged indole scaffold T Noreen, M Taha, S Imran, S Chigurupati, F Rahim, M Selvaraj, ... Bioorganic chemistry 72, 248-255, 2017 | 90 | 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 | 83 | 2017 |
| Synthesis of bis-indolylmethanes as new potential inhibitors of β-glucuronidase and their molecular docking studies M Taha, H Ullah, LMR Al Muqarrabun, MN Khan, F Rahim, N Ahmat, M Ali, ... European Journal of Medicinal Chemistry 143, 1757-1767, 2018 | 73 | 2018 |
| Bisindolylmethane thiosemicarbazides as potential inhibitors of urease: Synthesis and molecular modeling studies M Taha, H Ullah, LMR Al Muqarrabun, MN Khan, F Rahim, N Ahmat, ... Bioorganic & medicinal chemistry 26 (1), 152-160, 2018 | 72 | 2018 |
| Synthesis, in vitro alpha-glucosidase inhibitory potential of benzimidazole bearing bis-Schiff bases and their molecular docking study F Rahim, K Zaman, M Taha, H Ullah, M Ghufran, A Wadood, W Rehman, ... Bioorganic Chemistry 94, 103394, 2020 | 71 | 2020 |
| 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 |
| Synthesis of 2-acylated and sulfonated 4-hydroxycoumarins: in vitro urease inhibition and molecular docking studies U Rashid, F Rahim, M Taha, M Arshad, H Ullah, T Mahmood, M Ali Bioorganic Chemistry 66, 111-116, 2016 | 66 | 2016 |
| Synthesis, in vitro α-amylase, α-glucosidase activities and molecular docking study of new benzimidazole bearing thiazolidinone derivatives S Khan, H Ullah, F Rahim, M Nawaz, R Hussain, L Rasheed Journal of Molecular Structure 1269, 133812, 2022 | 65 | 2022 |
| Synthesis and biological evaluation of novel N-arylidenequinoline-3-carbohydrazides as potent β-glucuronidase inhibitors M Taha, S Sultan, HA Nuzar, F Rahim, S Imran, NH Ismail, H Naz, H Ullah Bioorganic & Medicinal Chemistry 24 (16), 3696-3704, 2016 | 65 | 2016 |
| Synthesis, in vitro urease inhibitory potential and molecular docking study of Benzimidazole analogues K Zaman, F Rahim, M Taha, H Ullah, A Wadood, M Nawaz, F Khan, ... Bioorganic Chemistry 89, 103024, 2019 | 62 | 2019 |
| Synthesis, in vitro bio-evaluation, and molecular docking study of thiosemicarbazone-based isatin/bis-Schiff base hybrid analogues as effective cholinesterase inhibitors S Khan, H Ullah, R Hussain, Y Khan, MU Khan, M Khan, A Sattar, ... Journal of Molecular Structure 1284, 135351, 2023 | 59 | 2023 |
| Development of bis-thiobarbiturates as successful urease inhibitors and their molecular modeling studies F Rahim, M Ali, S Ullah, U Rashid, H Ullah, M Taha, MT Javed, ... Chinese Chemical Letters 27 (5), 693-697, 2016 | 59 | 2016 |
