Scaffold hybridization in generation of indenoindolones as anticancer agents that induce apoptosis with cell cycle arrest at G2/M phase.

Abstract:

:Scaffold hybridization of several natural and synthetic anticancer leads led to the consideration of indenoindolones as potential novel anticancer agents. A series of these compounds were prepared by a diversity-feasible synthetic method. They were found to possess anticancer activities with higher potency compared to etoposide and 5-fluorouracil in kidney cancer cells (HEK 293) and low toxicity to corresponding normal cells (Vero). They exerted apoptotic effect with blocking of cell cycle at G2/M phase.

journal_name

Bioorg Med Chem Lett

authors

Kashyap M,Das D,Preet R,Mohapatra P,Satapathy SR,Siddharth S,Kundu CN,Guchhait SK

doi

10.1016/j.bmcl.2012.02.007

subject

Has Abstract

pub_date

2012-04-01 00:00:00

pages

2474-9

issue

7

eissn

0960-894X

issn

1464-3405

pii

S0960-894X(12)00190-4

journal_volume

22

pub_type

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