Literature DB >> 22863709

Design, synthesis and anticancer activities of diaryl urea derivatives bearing N-acylhydrazone moiety.

Bei Zhang1, Yanfang Zhao, Xin Zhai, Lihui Wang, Jingyu Yang, Zehui Tan, Ping Gong.   

Abstract

A new series of diaryl urea derivatives bearing N-acylhydrazone moiety were designed and synthesized. All the target compounds were evaluated for their cytotoxic activities in vitro against human lung adenocarcinoma epithelial cell line (A549), human breast cancer cell line (MDA-MB-231) and human leukemia cell line (HL-60) by standard 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Several compounds (1a, 1f and 1h) were further evaluated against human embryonic fibroblast, lung-derived cell line (WI38). The pharmacological results indicated that some compounds exhibited promising anticancer activities. In particular, compound 1f showed the most potent cytotoxicity against the tested three cell lines with IC(50) values of 0.41 µM, 0.24 µM and 0.23 µM, respectively.

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Year:  2012        PMID: 22863709     DOI: 10.1248/cpb.c12-00234

Source DB:  PubMed          Journal:  Chem Pharm Bull (Tokyo)        ISSN: 0009-2363            Impact factor:   1.645


  6 in total

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Authors:  Shanshan Shen; Hong Chen; Taofeng Zhu; Xiuqin Ma; Jun Xu; Wenjiao Zhu; Ruhua Chen; Jing Xie; Tieliang Ma; Lei Jia; Yuan Wang; Chunyan Peng
Journal:  Oncol Lett       Date:  2017-03-14       Impact factor: 2.967

2.  Removal of Metabolic Liabilities Enables Development of Derivatives of Procaspase-Activating Compound 1 (PAC-1) with Improved Pharmacokinetics.

Authors:  Howard S Roth; Rachel C Botham; Steven C Schmid; Timothy M Fan; Levent Dirikolu; Paul J Hergenrother
Journal:  J Med Chem       Date:  2015-04-20       Impact factor: 7.446

3.  Derivatives of Procaspase-Activating Compound 1 (PAC-1) and their Anticancer Activities.

Authors:  Howard S Roth; Paul J Hergenrother
Journal:  Curr Med Chem       Date:  2016       Impact factor: 4.530

4.  Design and Discovery of Quinazoline- and Thiourea-Containing Sorafenib Analogs as EGFR and VEGFR-2 Dual TK Inhibitors.

Authors:  Shaofeng Sun; Jingwen Zhang; Ningning Wang; Xiangkai Kong; Fenghua Fu; Hongbo Wang; Jianwen Yao
Journal:  Molecules       Date:  2017-12-23       Impact factor: 4.411

5.  Towards discovery of novel scaffold with potent antiangiogenic activity; design, synthesis of pyridazine based compounds, impact of hinge interaction, and accessibility of their bioactive conformation on VEGFR-2 activities.

Authors:  Maiy Y Jaballah; Rabah A T Serya; Nasser Saad; Sohair M Khojah; Marawan Ahmed; Khaled Barakat; Khaled A M Abouzid
Journal:  J Enzyme Inhib Med Chem       Date:  2019-12       Impact factor: 5.051

6.  Solid state characterization and theoretical study of non-linear optical properties of a Fluoro-N-Acylhydrazide derivative.

Authors:  Rosemberg F N Rodrigues; Leonardo R Almeida; Florisberto G Dos Santos; Paulo S Carvalho; Wanderson C de Souza; Kleber S Moreira; Gilberto L B de Aquino; Clodoaldo Valverde; Hamilton B Napolitano; Basílio Baseia
Journal:  PLoS One       Date:  2017-04-24       Impact factor: 3.240

  6 in total

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