Publications

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New Antiproliferative Pyrazole/Quinoline Hybrids: Design, Synthesis, and Biological Evaluation as EGFR Inhibitors

Chemical Biology & Drug Design | 2026

DOI: https://doi.org/10.1111/cbdd.70256

New antiproliferative 1,3,4-oxadiazole/benzimidazole derivatives: Design, synthesis, and biological evaluation as dual EGFR and BRAFV600E inhibitors

Bioorganic Chemistry | 2025

DOI: https://doi.org/10.1016/j.bioorg.2025.108297

Novel 1,2,4-oxadiazole/pyrrolidine hybrids as DNA gyrase and topoisomerase IV inhibitors with potential antibacterial activity

Arabian Journal of Chemistry | 2024

DOI: https://doi.org/10.1016/j.arabjc.2021.103538

New pyrimidine/thiazole hybrids endowed with analgesic, anti‐inflammatory, and lower cardiotoxic activities: Design, synthesis, and COX‐2/sEH dual inhibition

Arch. Pharm. | 2022

DOI: https://doi.org/10.1002/ardp.202200024

New 1,3,4‐oxadiazole‐chalcone/benzimidazole hybrids as potent antiproliferative agents

Arch. Pharm. | 2022

DOI: https://doi.org/10.1002/ardp.202200357

New 1,3,4‐oxadiazole‐chalcone/benzimidazole hybrids as potent antiproliferative agents

Archiv der Pharmazi | 2022

DOI: https://doi.org/10.1002/ardp.202200357

Novel indazole derivatives as potent apoptotic antiproliferative agents by multi-targeted mechanism: Synthesis and biological evaluation

Bioorganic Chemistry | 2022

DOI: https://doi.org/10.1016/j.bioorg.2022.105922

New 1,2,4‐oxadiazole/pyrrolidine hybrids as topoisomerase IV and DNA gyrase inhibitors with promising antibacterial activity

Arch. Pharm. | 2022

DOI: https://doi.org/10.1002/ardp.202100516

New1,3,4?oxadiazoles linked with the 1,2,3?triazole moiety as antiproliferative agents targeting the EGFR tyrosine kinase

Arch. Pharm | 2022

DOI: https://doi.org/10.1002/ardp.202200009

Novel 1,2,4-oxadiazole/pyrrolidine hybrids as DNA gyrase and topoisomerase IV inhibitors with potential antibacterial activity

Arabian Journal of Chemistry | 2021

DOI: https://doi.org/10.1016/j.arabjc.2021.103538

Novel 1,5-diaryl pyrazole-3-carboxamides as selective COX-2/sEH inhibitors with analgesic, anti-inflammatory, and lower cardiotoxicity effects

Bioorganic Chemistry | 2021

DOI: https://doi.org/10.1016/j.bioorg.2021.105302

New quinoline/1,2,4-triazole hybrids as dual inhibitors of COX-2/5-LOX and inflammatory cytokines: Design, synthesis, and docking study

Journal of Molecular Structure | 2021

DOI: https://doi.org/10.1016/j.molstruc.2021.130948

Novel 1,2,4-triazole derivatives as apoptotic inducers targeting p53: Synthesis and antiproliferative activity

Bioorganic Chemistry | 2020

DOI: https://doi.org/10.1016/j.bioorg.2020.104369