Cargando…
Antiproliferative S-Trityl-l-Cysteine -Derived Compounds as SIRT2 Inhibitors: Repurposing and Solubility Enhancement
S-trityl-l-cysteine (STLC) is a well-recognized lead compound known for its anticancer activity owing to its potent inhibitory effect on human mitotic kinesin Eg5. STLC contains two free terminal amino and carboxyl groups that play pivotal roles in binding to the Eg5 pocket. On the other hand, such...
Autores principales: | Radwan, Mohamed O., Ciftci, Halil I., Ali, Taha F. S., Ellakwa, Doha E., Koga, Ryoko, Tateishi, Hiroshi, Nakata, Akiko, Ito, Akihiro, Yoshida, Minoru, Okamoto, Yoshinari, Fujita, Mikako, Otsuka, Masami |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6766826/ https://www.ncbi.nlm.nih.gov/pubmed/31510043 http://dx.doi.org/10.3390/molecules24183295 |
Ejemplares similares
-
In Vitro and In Silico Evaluation of Anticancer Activity of New Indole-Based 1,3,4-Oxadiazoles as EGFR and COX-2 Inhibitors
por: Sever, Belgin, et al.
Publicado: (2020) -
Introduction of H2C2‐type zinc‐binding residues into HIV‐2 Vpr increases its expression level
por: Koga, Ryoko, et al.
Publicado: (2017) -
Design, Synthesis and Biological Evaluation of Pentacyclic Triterpene Derivatives: Optimization of Anti-ABL Kinase Activity
por: I. Ciftci, Halil, et al.
Publicado: (2019) -
In-Cell Trityl–Trityl Distance Measurements
on Proteins
por: Yang, Yin, et al.
Publicado: (2020) -
Design, Synthesis, and Biological Evaluation of Novel 1,3,4-Thiadiazole Derivatives as Potential Antitumor Agents against Chronic Myelogenous Leukemia: Striking Effect of Nitrothiazole Moiety
por: Altıntop, Mehlika Dilek, et al.
Publicado: (2017)