Synthesis, anticancer activities and molecular modeling studies of novel indole retinoid derivatives

Date

2012

Authors

Gurkan-Alp, A. S.
Mumcuoglu, M.
Andac, C. A.
Dayanc, E.
Cetin Atalay, R.
Buyukbingol, E.

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Source Title

European Journal of Medicinal Chemistry

Print ISSN

0223-5234

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Publisher

Elsevier

Volume

58

Issue

Pages

346 - 354

Language

English

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Abstract

In this study, novel (E)-3-(5-substituted-1H-indol-3-yl)-1-(5,5,8,8- tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl)prop-2-en-1-one (5(a-e)) derivatives were synthesized and their anticancer effects were determined in vitro. Novel indole retinoid compounds except 5e have anti-proliferative capacity in liver, breast and colon cancer cell lines. This anti-proliferative effect was further analyzed in breast cancer cell line panel by using the most potent compound 5a. It was determined that 5a can inhibit proliferation at very low IC50 concentrations in all of the breast cancer cell lines. Here, we present some evidence on apoptotic termination of cancer cell proliferation which may be primarily driven by the inhibition of RXRα and, to a lesser extent, RXRγ. © 2012 Elsevier Masson SAS. All rights reserved.

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Published Version (Please cite this version)