Literature DB >> 22000922

Design, synthesis and biological evaluation of substituted 11H-benzo[a]carbazole-5-carboxamides as novel antitumor agents.

Yu-Qin Wang1, Xiao-Hua Li, Qian He, Yi Chen, Yu-Yuan Xie, Jian Ding, Ze-Hong Miao, Chun-Hao Yang.   

Abstract

A series of novel 11H-benzo[a]carbazole-5-carboxamide derivatives were designed, synthesized and evaluated for their antitumor activity against human cancer A549 and HCT-116 cell lines. Most of the compounds showed potent antitumor activities, and compound 8 displayed remarkable in vitro and in vivo anticancer activity comparable to that of amonafide.
Copyright © 2011 Elsevier Masson SAS. All rights reserved.

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Year:  2011        PMID: 22000922     DOI: 10.1016/j.ejmech.2011.09.050

Source DB:  PubMed          Journal:  Eur J Med Chem        ISSN: 0223-5234            Impact factor:   6.514


  2 in total

1.  NHC-Ni(II)-catalyzed cyclopropene-isocyanide [5 + 1] benzannulation.

Authors:  Jian-Qiang Huang; Meng Yu; Xuefeng Yong; Chun-Yu Ho
Journal:  Nat Commun       Date:  2022-07-16       Impact factor: 17.694

2.  Crystal structure of 9-butyl-3-(9-butyl-9H-carbazol-3-yl)-9H-carbazole.

Authors:  K Stalindurai; C Ramalingan; B Sridhar; S Selvanayagam
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2014-11-21
  2 in total

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