| 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 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 | 177 | 2014 |
| 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 of novel flavone hydrazones: In-vitro evaluation of α-glucosidase inhibition, QSAR analysis and docking studies S Imran, M Taha, NH Ismail, SM Kashif, F Rahim, W Jamil, M Hariono, ... European journal of medicinal chemistry 105, 156-170, 2015 | 130 | 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 of novel inhibitors of β-glucuronidase based on benzothiazole skeleton and study of their binding affinity by molecular docking KM Khan, F Rahim, SA Halim, M Taha, M Khan, S Perveen, MA Mesaik, ... Bioorganic & medicinal chemistry 19 (14), 4286-4294, 2011 | 118 | 2011 |
| 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, α-glucosidase inhibition and molecular docking study of coumarin based derivatives M Taha, SAA Shah, M Afifi, S Imran, S Sultan, F Rahim, KM Khan Bioorganic Chemistry 77, 586-592, 2018 | 104 | 2018 |
| 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 |
| Benzimidazole derivatives as new α-glucosidase inhibitors and in silico studies NKNA Zawawi, M Taha, N Ahmat, A Wadood, NH Ismail, F Rahim, ... Bioorganic Chemistry 64, 29-36, 2016 | 96 | 2016 |
| 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 |
| Synthesis of novel derivatives of 4-methylbenzimidazole and evaluation of their biological activities M Taha, NH Ismail, W Jamil, H Rashwan, SM Kashif, AA Sain, MI Adenan, ... European journal of medicinal chemistry 84, 731-738, 2014 | 89 | 2014 |
| Synthesis of novel derivatives of oxindole, their urease inhibition and molecular docking studies M Taha, NH Ismail, A Khan, SAA Shah, A Anwar, SA Halim, MQ Fatmi, ... Bioorganic & Medicinal Chemistry Letters 25 (16), 3285-3289, 2015 | 84 | 2015 |
| 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, molecular docking and α-glucosidase inhibition of 5-aryl-2-(6′-nitrobenzofuran-2′-yl)-1, 3, 4-oxadiazoles M Taha, NH Ismail, S Imran, A Wadood, F Rahim, SM Saad, KM Khan, ... Bioorganic chemistry 66, 117-123, 2016 | 81 | 2016 |
| Acylhydrazide Schiff bases: DPPH radical and superoxide anion scavengers K Mohammed Khan, M Taha, F Naz, S Siddiqui, S Ali, F Rahim, ... Medicinal Chemistry 8 (4), 705-710, 2012 | 80* | 2012 |
| Synthesis crystal structure of 2-methoxybenzoylhydrazones and evaluation of their α-glucosidase and urease inhibition potential M Taha, NH Ismail, MS Baharudin, S Lalani, S Mehboob, KM Khan, ... Medicinal Chemistry Research 24, 1310-1324, 2015 | 76 | 2015 |
