| Antioxidant, cytotoxic and antimicrobial activities of green synthesized silver nanoparticles from crude extract of Bergenia ciliata AR Phull, Q Abbas, A Ali, H Raza, M Zia, I Haq Future Journal of Pharmaceutical Sciences 2 (1), 31-36, 2016 | 254 | 2016 |
| Exploration of novel human tyrosinase inhibitors by molecular modeling, docking and simulation studies M Hassan, Z Ashraf, Q Abbas, H Raza, SY Seo Interdisciplinary sciences: computational life sciences 10, 68-80, 2018 | 97 | 2018 |
| Synthesis, molecular docking studies of coumarinyl-pyrazolinyl substituted thiazoles as non-competitive inhibitors of mushroom tyrosinase A Saeed, PA Mahesar, PA Channar, Q Abbas, FA Larik, M Hassan, ... Bioorganic Chemistry 74, 187-196, 2017 | 60 | 2017 |
| The exploration of novel Alzheimer’s therapeutic agents from the pool of FDA approved medicines using drug repositioning, enzyme inhibition and kinetic mechanism approaches M Hassan, H Raza, MA Abbasi, AA Moustafa, SY Seo Biomedicine & Pharmacotherapy 109, 2513-2526, 2019 | 50 | 2019 |
| Sulfonamide-linked ciprofloxacin, sulfadiazine and amantadine derivatives as a novel class of inhibitors of jack bean urease; synthesis, kinetic mechanism and molecular docking PA Channar, A Saeed, F Albericio, FA Larik, Q Abbas, M Hassan, H Raza, ... Molecules 22 (8), 1352, 2017 | 47 | 2017 |
| Hybrid pharmacophoric approach in the design and synthesis of coumarin linked pyrazolinyl as urease inhibitors, kinetic mechanism and molecular docking A Saeed, PA Mahesar, PA Channar, FA Larik, Q Abbas, M Hassan, ... Chemistry & biodiversity 14 (8), e1700035, 2017 | 45 | 2017 |
| Novel C-2 symmetric molecules as α-glucosidase and α-amylase inhibitors: design, synthesis, kinetic evaluation, molecular docking and pharmacokinetics D Shahzad, A Saeed, FA Larik, PA Channar, Q Abbas, MF Alajmi, ... Molecules 24 (8), 1511, 2019 | 43 | 2019 |
| Long chain 1-acyl-3-arylthioureas as jack bean urease inhibitors, synthesis, kinetic mechanism and molecular docking studies A Saeed, S Rehman, PA Channar, FA Larik, Q Abbas, M Hassan, H Raza, ... Journal of the Taiwan Institute of Chemical Engineers 77, 54-63, 2017 | 42 | 2017 |
| Jack bean urease inhibitors, and antioxidant activity based on palmitic acid derived 1-acyl-3-arylthioureas: Synthesis, kinetic mechanism and molecular docking studies A Saeed, PA Channar, FA Larik, Q Abbas, M Hassan, H Raza, SY Seo Drug research 67 (10), 596-605, 2017 | 38 | 2017 |
| Synthesis of sulfadiazinyl acyl/aryl thiourea derivatives as calf intestinal alkaline phosphatase inhibitors, pharmacokinetic properties, lead optimization, Lineweaver-Burk … A Saeed, G Saddique, PA Channar, FA Larik, Q Abbas, M Hassan, ... Bioorganic & Medicinal Chemistry 26 (12), 3707-3715, 2018 | 36 | 2018 |
| Drug-1, 3, 4-thiadiazole conjugates as novel mixed-type inhibitors of acetylcholinesterase: Synthesis, molecular docking, pharmacokinetics, and ADMET evaluation R Ujan, A Saeed, PA Channar, FA Larik, Q Abbas, MF Alajmi, ... Molecules 24 (5), 860, 2019 | 34 | 2019 |
| Synthesis of novel N-(1, 3-thiazol-2-yl) benzamide clubbed oxadiazole scaffolds: Urease inhibition, Lipinski rule and molecular docking analyses MA Abbasi, H Raza, SZ Siddiqui, SAA Shah, M Hassan, SY Seo Bioorganic chemistry 83, 63-75, 2019 | 33 | 2019 |
| Isolation, characterization, and in silico, in vitro and in vivo antiulcer studies of isoimperatorin crystallized from Ostericum koreanum H Raza, Q Abbas, M Hassan, SH Eo, Z Ashraf, D Kim, AR Phull, SJ Kim, ... Pharmaceutical biology 55 (1), 218-226, 2017 | 31 | 2017 |
| Acetazolamide Inhibits the Level of Tyrosinase and Melanin: An Enzyme Kinetic, In Vitro, In Vivo, and In Silico Studies Q Abbas, H Raza, M Hassan, AR Phull, SJ Kim, SY Seo Chemistry & Biodiversity 14 (9), e1700117, 2017 | 30 | 2017 |
| Novel adamantyl clubbed iminothiazolidinones as promising elastase inhibitors: design, synthesis, molecular docking, ADMET and DFT studies A Ahmed, A Saeed, SA Ejaz, M Aziz, MZ Hashmi, PA Channar, Q Abbas, ... RSC advances 12 (19), 11974-11991, 2022 | 29 | 2022 |
| Synthesis and structure-activity relationship of tyrosinase inhibiting novel bi-heterocyclic acetamides: Mechanistic insights through enzyme inhibition, kinetics and … ARS Butt, MA Abbasi, SZ Siddiqui, H Raza, M Hassan, SAA Shah, ... Bioorganic chemistry 86, 459-472, 2019 | 25 | 2019 |
| Novel 1, 3‐oxazine‐tetrazole hybrids as mushroom tyrosinase inhibitors and free radical scavengers: Synthesis, kinetic mechanism, and molecular docking studies R Qamar, A Saeed, FA Larik, Q Abbas, M Hassan, H Raza, SY Seo Chemical biology & drug design 93 (2), 123-131, 2019 | 25 | 2019 |
| Facile synthesis of new quinazolinone benzamides as potent tyrosinase inhibitors: Comparative spectroscopic and molecular docking studies PG Mahajan, NC Dige, BD Vanjare, H Raza, M Hassan, SY Seo, CH Kim, ... Journal of Molecular Structure 1198, 126915, 2019 | 24 | 2019 |
| Ultrasound mediated efficient synthesis of new 4-oxoquinazolin-3 (4H)-yl) furan-2-carboxamides as potent tyrosinase inhibitors: Mechanistic approach through chemoinformatics … NC Dige, PG Mahajan, H Raza, M Hassan, BD Vanjare, H Hong, KH Lee, ... Bioorganic chemistry 92, 103201, 2019 | 24 | 2019 |
| Novel 1, 2, 4-triazole analogues as mushroom tyrosinase inhibitors: Synthesis, kinetic mechanism, cytotoxicity and computational studies BD Vanjare, PG Mahajan, NC Dige, H Raza, M Hassan, Y Han, SJ Kim, ... Molecular Diversity 25, 2089-2106, 2021 | 21 | 2021 |
Mubasher HassanThe Steve and Cindy Rasmussen Institute for Genomic Medicine, Nationwide Children HospitalBestätigte E-Mail-Adresse bei nationwidechildrens.org
