Exploration of the SAR of anti-invasive chalcones: Synthesis and biological evaluation of conformationally restricted analogues

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Abstract

In order to get a clearer view on the active geometry of anti-invasive chalcones, we have prepared a number of isoxazoles and related substances as conformationally restrained mimics of 1,3-diarylpropenones, and also of (Z)-stilbenes. In vitro anti-invasive activity data for 3,5-isoxazoles and 4,5-isoxazoles, together with an in silico geometrical comparison, point towards an active conformation for chalcones more resembling their s-trans geometry than the s-cis counterpart. © 2012 Elsevier Ltd. All rights reserved.

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Roman, B. I., Ryck, T. D., Dierickx, L., Vanhoecke, B. W. A., Katritzky, A. R., Bracke, M., & Stevens, C. V. (2012). Exploration of the SAR of anti-invasive chalcones: Synthesis and biological evaluation of conformationally restricted analogues. Bioorganic and Medicinal Chemistry, 20(15), 4812–4819. https://doi.org/10.1016/j.bmc.2012.05.069

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