Cargando…
Design, Synthesis and Biological Evaluation of Jahanyne Analogs as Cell Cycle Arrest Inducers
Jahanyne, a lipopeptide with a unique terminal alkynyl and OEP (2-(1-oxo-ethyl)-pyrrolidine) moiety, exhibits anticancer activity. We synthesized jahanyne and analogs modified at the OEP moiety, employing an α-fluoromethyl ketone (FMK) strategy. Preliminary bioassays indicated that compound 1b (FMK–...
Autores principales: | Ye, Baijun, Gong, Jianmiao, Li, Qiuying, Bao, Shiqi, Zhang, Xuemei, Chen, Jing, Meng, Qing, Chen, Bolin, Jiang, Peng, Wang, Liang, Chen, Yue |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7142928/ https://www.ncbi.nlm.nih.gov/pubmed/32210159 http://dx.doi.org/10.3390/md18030176 |
Ejemplares similares
-
Total Synthesis of Desmethyl
Jahanyne and Its Lipo-Tetrapeptide
Conjugates Derived from Parent Skeleton as BCL-2-Mediated Apoptosis-Inducing
Agents
por: Kallepu, Shivakrishna, et al.
Publicado: (2018) -
Design and synthesis of novel cytotoxic fluoroquinolone analogs through topoisomerase inhibition, cell cycle arrest, and apoptosis
por: Elanany, Mohamed A., et al.
Publicado: (2023) -
Synthesis and Biological Evaluation of Novel Benzimidazole Derivatives and Analogs Targeting the NLRP3 Inflammasome
por: Pan, Liangkun, et al.
Publicado: (2017) -
Studies toward the Total Synthesis of Itralamide B and Biological Evaluation of Its Structural Analogs
por: Wang, Xiaoji, et al.
Publicado: (2015) -
Sulforaphane and Its Bifunctional Analogs: Synthesis and Biological Activity
por: Janczewski, Łukasz
Publicado: (2022)