Synthesis and anticancer activity of ...
Document type :
Article dans une revue scientifique
PMID :
Permalink :
Title :
Synthesis and anticancer activity of analogues of phenstatin, with a phenothiazine A-ring, as a new class of microtubule-targeting agents
Author(s) :
Abuhaie, Cristina-Maria [Auteur]
Bicu, Elena [Auteur]
Rigo, Benoit [Auteur]
Gautret, Philippe [Auteur]
Belei, Dalila [Auteur]
Farce, Amaury [Auteur]
Dubois, Joelle [Auteur]
Ghinet, Alina [Auteur]
Bicu, Elena [Auteur]
Rigo, Benoit [Auteur]
Gautret, Philippe [Auteur]
Belei, Dalila [Auteur]
Farce, Amaury [Auteur]

Dubois, Joelle [Auteur]
Ghinet, Alina [Auteur]

Journal title :
Bioorganic & Medicinal Chemistry Letters
Abbreviated title :
Bioorg. Med. Chem. Lett.
Volume number :
23
Pages :
147-152
Publication date :
2013-01-01
ISSN :
0960-894X
English keyword(s) :
Tubulin
Microtubule-targeting agent
Phenothiazine derivative
Anticancer agent
Microtubule-targeting agent
Phenothiazine derivative
Anticancer agent
HAL domain(s) :
Sciences du Vivant [q-bio]
English abstract : [en]
A new family of microtubule-targeting agents with a phenothiazine A-ring was synthesized and evaluated for anti-proliferative activity and interaction with tubulin. These new derivatives showed significant activities against ...
Show more >A new family of microtubule-targeting agents with a phenothiazine A-ring was synthesized and evaluated for anti-proliferative activity and interaction with tubulin. These new derivatives showed significant activities against cellular proliferation and tubulin polymerization, rather similar to those of phenstatin. Phenothiazine derivative 21 proved to be the most potent compound synthesized with GI(50) values ranging from 29 to 93 nM on different cell lines. The same compound showed a better inhibition of COLO 205, A498, and MCF7 cell lines than the parent phenstatin.Show less >
Show more >A new family of microtubule-targeting agents with a phenothiazine A-ring was synthesized and evaluated for anti-proliferative activity and interaction with tubulin. These new derivatives showed significant activities against cellular proliferation and tubulin polymerization, rather similar to those of phenstatin. Phenothiazine derivative 21 proved to be the most potent compound synthesized with GI(50) values ranging from 29 to 93 nM on different cell lines. The same compound showed a better inhibition of COLO 205, A498, and MCF7 cell lines than the parent phenstatin.Show less >
Audience :
Internationale
Popular science :
Non
Administrative institution(s) :
CHU Lille
Inserm
Université de Lille
Inserm
Université de Lille
Research team(s) :
Therapeutic innovation targetting inflammation
Submission date :
2019-05-17T13:14:31Z