Cargando…
Phenothiazine- and Carbazole-Cyanochalcones as Dual Inhibitors of Tubulin Polymerization and Human Farnesyltransferase
In the search for innovative approaches to cancer chemotherapy, a chemical library of 49 cyanochalcones, 1a-r, 2a-o, and 3a-p, was designed as dual inhibitors of human farnesyltransferase (FTIs) and tubulin polymerization (MTIs) (FTIs/MTIs), two important biological targets in oncology. This approac...
Autores principales: | Zubaș, Andreea, Ghinet, Alina, Farce, Amaury, Dubois, Joëlle, Bîcu, Elena |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10305003/ https://www.ncbi.nlm.nih.gov/pubmed/37375835 http://dx.doi.org/10.3390/ph16060888 |
Ejemplares similares
-
Modified Methods for the Synthesis of Carbazole from Phenothiazine
por: Miller, R. Bryan, et al.
Publicado: (2001) -
7-Chloroquinolinehydrazones as First-in-Class Anticancer Experimental Drugs in the NCI-60 Screen among Different Investigated Series of Aryl, Quinoline, Pyridine, Benzothiazole and Imidazolehydrazones
por: Negru (Apostol), Georgiana, et al.
Publicado: (2023) -
Bacteria Are New Targets for Inhibitors of Human Farnesyltransferase
por: Weber, Lea, et al.
Publicado: (2021) -
Antitumour potential of BPT: a dual inhibitor of cdk4 and tubulin polymerization
por: Mahale, S, et al.
Publicado: (2015) -
Quinazolinone-Amino Acid Hybrids as Dual Inhibitors of EGFR Kinase and Tubulin Polymerization
por: Zayed, Mohamed F., et al.
Publicado: (2018)