Cargando…
Structure-based design, synthesis, and biological evaluation of novel piperine–resveratrol hybrids as antiproliferative agents targeting SIRT-2
A series of novel piperine–resveratrol hybrids 5a–h was designed, synthesized, and structurally elucidated by IR, and (1)H, (13)C, and (19)F NMR. Antiproliferative activities of 5a–h were evaluated by NCI against sixty cancer cell lines. Compound 5b, possessing resveratrol pharmacophoric phenolic mo...
Autores principales: | Tantawy, Ahmed H., Meng, Xiang-Gao, Marzouk, Adel A., Fouad, Ali, Abdelazeem, Ahmed H., Youssif, Bahaa G. M., Jiang, Hong, Wang, Man-Qun |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9037111/ https://www.ncbi.nlm.nih.gov/pubmed/35478872 http://dx.doi.org/10.1039/d1ra04061h |
Ejemplares similares
-
Novel piperine-carboximidamide hybrids: design, synthesis, and antiproliferative activity via a multi-targeted inhibitory pathway
por: Al-Wahaibi, Lamya H., et al.
Publicado: (2022) -
Design, Synthesis, Biological Evaluation, and Computational Studies of Novel Tri-Aryl Imidazole-Benzene Sulfonamide Hybrids as Promising Selective Carbonic Anhydrase IX and XII Inhibitors
por: Al-Wahaibi, Lamya H., et al.
Publicado: (2021) -
Design, Synthesis, and Biological Evaluation of Indole-2-carboxamides as Potential Multi-Target Antiproliferative Agents
por: Al-Wahaibi, Lamya H., et al.
Publicado: (2023) -
Design, Synthesis, and Biological Evaluation of Novel 3-Cyanopyridone/Pyrazoline Hybrids as Potential Apoptotic Antiproliferative Agents Targeting EGFR/BRAF(V600E) Inhibitory Pathways
por: Al-Wahaibi, Lamya H., et al.
Publicado: (2023) -
Biological Mechanisms by Which Antiproliferative Actions of Resveratrol Are Minimized
por: Ho, Yih, et al.
Publicado: (2017)