Indolizine and annulated indolizine derivatives incorporating a cyclopropylcarbonyl group were synthesized in a one pot procedure by the tanden reactions of [3 + 2] cycloaddition of the corresponding N-ylide with electron deficient alkene. Seventeen indolizine derivatives were reported for the first time. All the compounds were examined for their antiproliferative activity against the human hepatocellular liver carcinoma (Hep-G2) cell line by MTT method. Among the compounds tested, 5a, 5d, 5g and 5j showed the most favorable activities with IC50 values of 0.39, 0.48, 0.29 and 0.20 mu g/mL. Especially, compound 5j displayed potent antiproliferative activities with IC50 value of 0.20 mu g/mL, and showed significant EGFR kinase inhibitory activity with IC50 value of 0.085 mu M. Docking simulations of 5j were carried out to illustrate the binding mode of the molecular into the EGFR active site. (C) 2010 Elsevier Masson SAS. All rights reserved.
EP1578424A4
申请人:——
公开号:EP1578424A4
公开(公告)日:2007-08-08
SUBSTITUTED 1-BENZOYL-3-CYANO-PYRROLO 1,2-A] QUINOLINES AND ANALOGS AS ACTIVATORS OF CASPASES AND INDUCERS OF APOPTOSIS
申请人:Cytovia, Inc.
公开号:EP1578424A2
公开(公告)日:2005-09-28
US7135480B2
申请人:——
公开号:US7135480B2
公开(公告)日:2006-11-14
[EN] SUBSTITUTED 1-BENZOYL-3-CYANO-PYRROLO[1,2-A] QUINOLINES AND ANALOGS AS ACTIVATORS OF CASPASES AND INDUCERS OF APOPTOSIS<br/>[FR] 1-BENZOYLE-3-CYANO-PYRROLO[1,2-A] QUINOLINES SUBSTITUEES ET LEURS ANALOGUES, COMME ACTIVATEURS DE CASPASES ET INDUCTEURS D'APOPTOSE
申请人:CYTOVIA INC
公开号:WO2004055163A2
公开(公告)日:2004-07-01
The present invention is directed to substituted 1-benzoyl-3-cyano-pyrrolo[1,2-a]quinolines and analogs thereof as defined herein. The present invention also relates to the discovery that compounds of the invention are activators of caspases and inducers of apoptosis. Therefore, the activators of caspases and inducers of apoptosis of this invention can be used to induce cell death in a variety of clinical conditions in which uncontrolled growth and spread of abnormal cells occurs.