Literature DB >> 33979690

Design, synthesis and in vitro antitumor evaluation of novel pyrazole-benzimidazole derivatives.

Bo Ren1, Rong-Chun Liu1, Kegong Ji1, Jiang-Jiang Tang2, Jin-Ming Gao1.   

Abstract

A series of novel pyrazole-benzimidazole derivatives (6-42) have been designed, synthesized and evaluated for their in vitro antiproliferative activity against the HCT116, MCF-7 and Huh-7 cell lines. Among them, compounds 17, 26 and 35 showed significant antiproliferative activity against HCT116 cell lines with the IC50 values of 4.33, 5.15 and 4.84 μM, respectively. Moreover, fluorescent staining studies showed compound 17 could induce cancer cells apoptosis. The flow cytometry assay revealed that compound 17 could induce cell cycle arrest at G0/G1 phase. All in all, these consequences suggest that pyrazole-benzimidazole derivatives could serve as promising compounds for further research to develop novel and highly potent cancer therapy agents.
Copyright © 2021 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Antiproliferative activity; Benzimidazole-pyrazole; Cell cycle; Cells apoptosis

Year:  2021        PMID: 33979690     DOI: 10.1016/j.bmcl.2021.128097

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


  1 in total

1.  Synthesis, DFT Molecular Geometry and Anticancer Activity of Symmetrical 2,2'-(2-Oxo-1H-benzo[d]imidazole-1,3(2H)-diyl) Diacetate and Its Arylideneacetohydrazide Derivatives.

Authors:  Manel Dhahri; Firdos Alam Khan; Abdul-Hamid Emwas; Rua B Alnoman; Mariusz Jaremko; Nadjet Rezki; Mohamed Reda Aouad; Mohamed Hagar
Journal:  Materials (Basel)       Date:  2022-03-30       Impact factor: 3.623

  1 in total

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