• English
    • français
  • Help
  •  | 
  • Contact
  •  | 
  • About
  •  | 
  • Login
  • HAL portal
  •  | 
  • Pages Pro
  • EN
  •  / 
  • FR
View Item 
  •   LillOA Home
  • Liste des unités
  • Institut de Recherche Translationnelle sur l'Inflammation (INFINITE) - U1286
  • View Item
  •   LillOA Home
  • Liste des unités
  • Institut de Recherche Translationnelle sur l'Inflammation (INFINITE) - U1286
  • View Item
JavaScript is disabled for your browser. Some features of this site may not work without it.

Synthesis and anticancer activity of ...
  • BibTeX
  • CSV
  • Excel
  • RIS

Document type :
Article dans une revue scientifique
DOI :
10.1016/j.bmcl.2012.10.135
PMID :
23200248
Permalink :
http://hdl.handle.net/20.500.12210/11243
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] refId
Dubois, Joelle [Auteur]
Ghinet, Alina [Auteur] refId
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
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 >
Audience :
Internationale
Popular science :
Non
Administrative institution(s) :
CHU Lille
Inserm
Université de Lille
Collections :
  • Institut de Recherche Translationnelle sur l'Inflammation (INFINITE) - U1286
Research team(s) :
Therapeutic innovation targetting inflammation
Submission date :
2019-05-17T13:14:31Z
Université de Lille

Mentions légales
Université de Lille © 2017