Design, synthesis and evaluation of (E)-α-benzylthio chalcones as novel inhibitors of BCR-ABL kinase
摘要:
Novel (E)-alpha-benzylthio chalcones are reported with preliminary in vitro activity data indicating that several of them are potent inhibitors (comparable to imatinib, the reference compound) of BCR-ABL phosphorylation in leukemic K562 cells, known to express high levels of BCR-ABL. The ability of such compounds to significantly inhibit K562 cell proliferation suggests that this scaffold could be a promising lead for the development of anticancer agents that are able to block BCR-ABL phosphorylation in leukemic cells. (C) 2010 Elsevier Ltd. All rights reserved.
SULFIDE, SULFOXIDE AND SULFONE CHALCONE ANALOGUES, DERIVATIVES THEREOF AND THERAPEUTIC USES THEREOF
申请人:Reddy E. Premkumar
公开号:US20100028368A1
公开(公告)日:2010-02-04
Compounds useful as antiproliferative agents according to formula (I): wherein Ar
1
, Ar
2
, Ar
3
, m and n are as defined herein, salts, antibody conjugates, pharmaceutical compositions, methods of treatment, and synthetic methods are provided.
[EN] SULFIDE, SULFOXIDE AND SULFONE CHALCONE ANALOGUES, DERIVATIVES THEREOF AND THERAPEUTIC USES THEREOF<br/>[FR] ANALOGUES DE SULFURE, SULFOXYDE ET SULFONE DE CHALCONE, LEURS DÉRIVÉS ET LEURS UTILISATIONS THÉRAPEUTIQUES
申请人:UNIV TEMPLE
公开号:WO2008076270A2
公开(公告)日:2008-06-26
[EN] Compounds useful as antiproliferative agents according to formula (I): wherein Ar1, Ar2, Ar3, m and n are as defined herein, salts, antibody conjugates, pharmaceutical compositions, methods of treatment, and synthetic methods are provided. [FR] La présente invention a pour objet des composés utiles en tant qu'agents antiprolifératifs selon la formule (I): dans laquelle Ar1, Ar2, Ar3, m et n sont tels que définis dans la présente description, des sels, des conjugués d'anticorps, des compositions pharmaceutiques, des procédés de traitement et des procédés de synthèse.
Design, synthesis and evaluation of (E)-α-benzylthio chalcones as novel inhibitors of BCR-ABL kinase
作者:M.V. Ramana Reddy、Venkat R. Pallela、Stephen C. Cosenza、Muralidhar R. Mallireddigari、Revathi Patti、Marie Bonagura、May Truongcao、Balaiah Akula、Shashidhar S. Jatiani、E. Premkumar Reddy
DOI:10.1016/j.bmc.2010.01.051
日期:2010.3
Novel (E)-alpha-benzylthio chalcones are reported with preliminary in vitro activity data indicating that several of them are potent inhibitors (comparable to imatinib, the reference compound) of BCR-ABL phosphorylation in leukemic K562 cells, known to express high levels of BCR-ABL. The ability of such compounds to significantly inhibit K562 cell proliferation suggests that this scaffold could be a promising lead for the development of anticancer agents that are able to block BCR-ABL phosphorylation in leukemic cells. (C) 2010 Elsevier Ltd. All rights reserved.