| عنوان البحث | ملخص البحث |
| New benzothieno[2,3-c]pyridines as nonsteroidal CYP17 inhibitors: Design, synthesis, screening, apoptosis induction | |
| From triazolophthalazines to triazoloquinazolines: A bioisosterism-guided approach toward the identification of novel PCAF inhibitors with potential anticancer activity, | |
| 1,2,4-Triazolo[4,3-c]quinazolines: A bioisosterism-guided approach towards the development of novel PCAF inhibitors with potential anticancer activity, | |
| Synthesis, molecular modeling and biological evaluation of new benzo[4,5] thieno[3,2-b]pyran derivatives as topoisomerase I-DNA binary complex poisons | |
| In vivo‐ and in silico‐driven identification of novel synthetic quinoxalines as anticonvulsants and AMPA inhibitors, | |
| Potential antiviral and anticancer effect of imidazoles and bridgehead imidazoles generated by HPV-Induced cervical carcinomas via reactivating the P53/ pRb pathway and inhibition of CA IX, Aisha Y. | |
| Comprehensive review for anticancer hybridized multitargeting HDAC | |
| 3-Cyano-2-oxa-pyridines: a promising template for diverse pharmacological Activities | |
| Utility of Activated Nitriles in the Synthesis of some New Pyridine and Fused Pyridine Derivatives with Anticancer Activity | |
| Synthesis and Anticancer Activity Study of Some Novel Substituted and
Fused Pyridotriazepine Derivatives | |
| Utility of 2-Methyl-quinazolin-4(3H)-one in the Synthesis of Heterocyclic Compounds with Anticancer Activity. | |
| New benzothienopyran and benzothienopyranopyrimidine derivatives as topoisomerase I inhibitors: Design, synthesis, anticancer screening, apoptosis induction and molecular … | |
| Novel thioxoimidazolidinone derivatives as dual EGFR and CDK2 inhibitors: Design, synthesis, anticancer evaluation with in silico study | |
| Aminopyridone-linked benzimidazoles: a fragment-based drug design for the development of CDK9 inhibitors | |
| New Pyrimidine-5-Carbonitriles as COX-2 Inhibitors: Design, Synthesis, Anticancer Screening, Molecular Docking, and In Silico ADME Profile Studies | |
| Novel Aminopyrimidine-2, 4-diones, 2-Thiopyrimidine-4-ones, and 6-Arylpteridines as Dual-Target Inhibitors of BRD4/PLK1: Design, Synthesis, Cytotoxicity, and Computational Studies | |
| 4- Utilization of cyanopyridine in design and synthesis of first-in-class anticancer dual acting PIM-1 kinase/HDAC inhibitors, Bioorganic Chemistry 119, 105564 | |
| 1, 2, 4-Triazolo [4, 3-c] quinazolines: a bioisosterism-guided approach towards the development of novel PCAF inhibitors with potential anticancer activity | |
| In vivo‐and in silico‐driven identification of novel synthetic quinoxalines as anticonvulsants and AMPA inhibitors | |
| Utility of 2-methyl-quinazolin-4 (3H)-one in the synthesis of heterocyclic compounds with anticancer activity | |
| Potential antiviral and anticancer effect of imidazoles and bridgehead imidazoles generated by HPV-Induced cervical carcinomas via reactivating the P53/pRb pathway and … | |
| Synthesis and Anticancer Activity Study of Some Novel Substituted and Fused Pyridotriazepine Derivatives | |
| New benzothieno [2, 3-c] pyridines as nonsteroidal CYP17 inhibitors: Design, synthesis, anticancer screening, apoptosis induction and in silico ADME profile studies (vol 36, pg | |
| Design, synthesis and mechanistic study of new dual targeting HDAC/tubulin inhibitors | |
