Literature DB >> 30093295

Evaluation of 4-phenylamino-substituted naphthalene-1,2-diones as tubulin polymerization inhibitors.

Honghao Yang1, Baijiao An2, Xingshu Li3, Wei Zeng4.   

Abstract

A series of 4-phenylamino-substituted naphthalene-1,2-dione derivatives were prepared and evaluated as effective antiproliferative agents. MTT assays showed that the compounds with a methyl group on the nitrogen linker exhibited potent antiproliferative activities against human cancer cells. The mechanistic study revealed that these compounds could induce mitochondrial depolarization, which resulted in intracellular ROS production, and they also acted as tubulin polymerization inhibitors. Moreover, the typical compound could arrest A549 cells in the G2/M phase, resulting in cellular apoptosis and induced mitotic arrest in A549 cells through disrupting microtubule dynamics.
Copyright © 2018 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Antitumor agents; Mechanism; Reactive oxygen species; Tubulin polymerization inhibitors

Mesh:

Substances:

Year:  2018        PMID: 30093295     DOI: 10.1016/j.bmcl.2018.07.047

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


  2 in total

1.  Design, synthesis, and biological evaluation of novel 5,6,7-trimethoxy quinolines as potential anticancer agents and tubulin polymerization inhibitors.

Authors:  Salimeh Mirzaei; Farhad Eisvand; Farzin Hadizadeh; Fatemeh Mosaffa; Razieh Ghodsi
Journal:  Iran J Basic Med Sci       Date:  2020-12       Impact factor: 2.699

Review 2.  1,2-Naphthoquinone-4-sulfonic acid salts in organic synthesis.

Authors:  Ruan Carlos B Ribeiro; Patricia G Ferreira; Amanda de A Borges; Luana da S M Forezi; Fernando de Carvalho da Silva; Vitor F Ferreira
Journal:  Beilstein J Org Chem       Date:  2022-01-05       Impact factor: 2.883

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.