首页 | 本学科首页   官方微博 | 高级检索  
     检索      


Synthesis and Cytotoxic Activity Study of Novel 2-(Aryldiazenyl)-3-methyl-1H-benzo[g]indole Derivatives
Authors:Manar M Arafeh  Ebrahim Saeedian Moghadam  Sirin A I Adham  Raphael Stoll  Raid J Abdel-Jalil
Institution:1.Faculty of Pharmacy, Middle East University, Amman 11831, Jordan;2.Chemistry Department, College of Science, Sultan Qaboos University, Muscat 123, Oman;3.Biology Department, College of Science, Sultan Qaboos University, Muscat 123, Oman;4.Biomolecular NMR, Ruhr University of Bochum, D-44780 Bochum, Germany;
Abstract:A novel series of 2-(aryldiazenyl)-3-methyl-1H-benzog]indole derivatives (3a–f) were prepared through the cyclization of the corresponding arylamidrazones, employing polyphosphoric acid (PPA) as a cyclizing agent. All of the compounds (3a–f) were characterized using 1H NMR, 13C NMR, MS, elemental analysis, and melting point techniques. The synthesized compounds were evaluated for cytotoxic activity against diverse human cancer cell lines by the National Cancer Institute. While all of the screened compounds were found to be cytotoxic at a 10 µM concentration, two of them (2c) and (3c) were subjected to five dose screens and showed a significant cytotoxicity and selectivity.
Keywords:anti-cancer  synthesis  indole  heterocycles
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号