Synthesis, antimicrobial, and anti-inflammatory activity, of novel S-substituted and N-substituted 5-(1-adamantyl)-1,2,4-triazole-3-thiols ES Al-Abdullah, HH Asiri, S Lahsasni, EE Habib, TM Ibrahim, ... Drug design, development and therapy, 505-518, 2014 | 87 | 2014 |
Identification of novel oxadiazole-based benzothiazole derivatives as potent inhibitors of α-glucosidase and urease: synthesis, in vitro bio-evaluation and their in silico … Y Khan, A Maalik, W Rehman, R Hussain, S Khan, MM Alanazi, HH Asiri, ... Journal of Saudi Chemical Society 27 (4), 101682, 2023 | 16 | 2023 |
Ethyl 4-{[3-(adamantan-1-yl)-4-phenyl-5-sulfanylidene-4, 5-dihydro-1H-1, 2, 4-triazol-1-yl] methyl} piperazine-1-carboxylate ES Al-Abdullah, HH Asiri, AA El-Emam, SW Ng Structure Reports 68 (2), o531-o531, 2012 | 15 | 2012 |
Novel pyrrolo [2, 3-d] pyrimidine derivatives as multi-kinase inhibitors with VEGFR-2 selectivity AAA Alotaibi, HH Asiri, AFMM Rahman, MM Alanazi Journal of Saudi Chemical Society 27 (5), 101712, 2023 | 14 | 2023 |
3-(Adamantan-1-yl)-4-phenyl-1-[(4-phenylpiperazin-1-yl) methyl]-1H-1, 2, 4-triazole-5 (4H)-thione ES Al-Abdullah, HH Asiri, A El-Emam, SW Ng Structure Reports 68 (2), o345-o345, 2012 | 10 | 2012 |
2-{[5-(Adamantan-1-yl)-4-methyl-4H-1, 2, 4-triazol-3-yl] sulfanyl}-N, N-dimethylethanamine AA El-Emam, S Lahsasni, HH Asiri, CK Quah, HK Fun Structure Reports 68 (5), o1356-o1356, 2012 | 9 | 2012 |
3-(Adamantan-1-yl)-1-[(4-benzylpiperazin-1-yl) methyl]-4-phenyl-1H-1, 2, 4-triazole-5 (4H)-thione ES Al-Abdullah, HH Asiri, A El-Emam, SW Ng Structure Reports 68 (2), o344-o344, 2012 | 4 | 2012 |
5-(Adamantan-1-yl)-3-[(2-methoxyethyl) sulfanyl]-4-phenyl-4H-1, 2, 4-triazole AA El-Emam, ES Al-Abdullah, HH Asiri, S Chantrapromma, HK Fun Structure Reports 68 (8), o2326-o2326, 2012 | 3 | 2012 |
Discovery of 1H-benzo[d]imidazole-(halogenated)Benzylidenebenzohydrazide Hybrids as Potential Multi-Kinase Inhibitors TO Mirgany, HH Asiri, AFMM Rahman, MM Alanazi Pharmaceuticals 17 (7), 839, 2024 | 1 | 2024 |
Development of novel antibacterial agents through the design and synthesis of Aminoacyl tRNA Synthetase (AaRS) inhibitors HHA Asiri Cardiff University, 2020 | | 2020 |