Your browser doesn't support javascript.
loading
Discovery of novel indole derivatives that inhibit NEDDylation and MAPK pathways against gastric cancer MGC803 cells.
Fu, Dong-Jun; Cui, Xin-Xin; Zhu, Ting; Zhang, Yan-Bing; Hu, Yang-Yang; Zhang, Li-Rong; Wang, Sheng-Hui; Zhang, Sai-Yang.
Afiliação
  • Fu DJ; Modern Research Center for Traditional Chinese Medicine, School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 100029, China. Electronic address: zzufdj@sina.com.
  • Cui XX; School of Basic Medical Science, Zhengzhou University, Zhengzhou 450001, China.
  • Zhu T; School of Basic Medical Science, Zhengzhou University, Zhengzhou 450001, China.
  • Zhang YB; School of Basic Medical Science, Zhengzhou University, Zhengzhou 450001, China.
  • Hu YY; Faculty of Science, The University of Melbourne, Victoria 3010, Australia.
  • Zhang LR; School of Basic Medical Science, Zhengzhou University, Zhengzhou 450001, China; The Academy of Medical Science, Zhengzhou University, Zhengzhou 450001, China; Henan Institute of Advanced Technology, Zhengzhou University, Zhengzhou 450001, China.
  • Wang SH; School of Basic Medical Science, Zhengzhou University, Zhengzhou 450001, China; The Academy of Medical Science, Zhengzhou University, Zhengzhou 450001, China; Henan Institute of Advanced Technology, Zhengzhou University, Zhengzhou 450001, China.
  • Zhang SY; School of Basic Medical Science, Zhengzhou University, Zhengzhou 450001, China; The Academy of Medical Science, Zhengzhou University, Zhengzhou 450001, China; Henan Institute of Advanced Technology, Zhengzhou University, Zhengzhou 450001, China; State Key Laboratory of Pharmaceutical Biotechnology,
Bioorg Chem ; 107: 104634, 2021 02.
Article em En | MEDLINE | ID: mdl-33476867
ABSTRACT
A series of novel indole derivatives were synthesized and evaluated for their antiproliferative activity against three selected cancer cell lines (MGC803, EC-109 and PC-3). Among these analogues, 2-(5-methoxy-1H-indol-1-yl)-N-(4-methoxybenzyl)-N-(3,4,5-trimethoxyphenyl)acetamide (V7) showed the best inhibitory activity against MGC803 cells with an IC50 value of 1.59 µM. Cellular mechanisms elucidated that V7 inhibited colony formation, induced apoptosis and arrested cell cycle at G2/M phase. Importantly, indole analogue V7 inhibited NEDDylation pathway and MAPK pathway against MGC803 cells.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transdução de Sinais / Indóis / Antineoplásicos Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transdução de Sinais / Indóis / Antineoplásicos Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article