Literature DB >> 21733686

Antiproliferative activity and QSAR studies of a series of new 4-aminomethylidene derivatives of some pyrazol-5-ones.

Violeta Marković1, Slavica Erić, Tatjana Stanojković, Nevenka Gligorijević, Sandra Aranđelović, Nina Todorović, Snežana Trifunović, Nedeljko Manojlović, Ratomir Jelić, Milan D Joksović.   

Abstract

Twenty five 4-aminomethylidene derivatives obtained from 3-phenyl-2-pyrazolin-5-one and 1,3-diphenyl-2-pyrazolin-5-one were synthesized and tested for their antiproliferative activity against human breast cancer MDA-MB-361 and MDA-MB-453 cell lines. The compounds derived from 1,3-diphenyl-2-pyrazolin-5-one exhibited the most remarkable activity in the treatment of both cell lines. In vitro antiproliferative activities were accompanied by an important apoptotic fraction of both cell lines; also, compounds inhibited key endothelial cell functions implicated in invasion and angiogenesis. QSAR methods were performed in order to analyze the influence of structural features of the compounds investigated on the antiproliferative potential on MDA-MB-361 and MDA-MB-453 cancer cells. One-parameter heuristic analysis was performed and different whole molecule and fragmental descriptors were considered for rationalization of mechanism of interaction of these compounds with active place of hypothetical target included in tumorigenesis.
Copyright © 2011 Elsevier Ltd. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21733686     DOI: 10.1016/j.bmcl.2011.06.025

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  6 in total

1.  QSAR models of antiproliferative activity of imidazo[2,1-b][1,3,4]thiadiazoles in various cancer cell lines.

Authors:  Joanna Matysiak; Andrzej Niewiadomy
Journal:  Mol Divers       Date:  2016-10-08       Impact factor: 2.943

2.  Synthesis, in-vitro antimicrobial and antitubercular screening of Schiff bases of 3-amino-1-phenyl-4- [2-(4-phenyl-1,3-thiazol-2-yl) hydrazin-1-ylidene]-4,5-dihydro-1H-pyrazol-5-one.

Authors:  K K Sivakumar; A Rajasekaran
Journal:  J Pharm Bioallied Sci       Date:  2013-04

3.  An easy direct arylation of 5-pyrazolones.

Authors:  Hao Gong; Yiwen Yang; Zechao Wang; Chunxiang Kuang
Journal:  Beilstein J Org Chem       Date:  2013-10-08       Impact factor: 2.883

4.  Design, synthesis and the biological evaluation of new 1,3-thiazolidine-4-ones based on the 4-amino-2,3-dimethyl-1-phenyl-3-pyrazolin-5-one scaffold.

Authors:  Maria Apotrosoaei; Ioana Mirela Vasincu; Maria Dragan; Frédéric Buron; Sylvain Routier; Lenuta Profire
Journal:  Molecules       Date:  2014-09-04       Impact factor: 4.411

Review 5.  Pyrazolone structural motif in medicinal chemistry: Retrospect and prospect.

Authors:  Zefeng Zhao; Xufen Dai; Chenyang Li; Xiao Wang; Jiale Tian; Ying Feng; Jing Xie; Cong Ma; Zhuang Nie; Peinan Fan; Mingcheng Qian; Xirui He; Shaoping Wu; Yongmin Zhang; Xiaohui Zheng
Journal:  Eur J Med Chem       Date:  2019-11-16       Impact factor: 6.514

6.  Design of cinnamaldehyde amino acid Schiff base compounds based on the quantitative structure-activity relationship.

Authors:  Hui Wang; Mingyue Jiang; Shujun Li; Chung-Yun Hse; Chunde Jin; Fangli Sun; Zhuo Li
Journal:  R Soc Open Sci       Date:  2017-09-06       Impact factor: 2.963

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.