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Hemisynthesis of selected embelin analogs and investigation of their proapoptotic activity against cancer cells

Abstract : Embelin is a natural product, inhibitor of XIAP (X-chromosome-linked Inhibitor of APoptosis) with strong proapoptotic properties on cancer cells. In order to clarify the role of two OH groups on benzoquinone core, we have prepared by hemisynthesis close analogs of embelin, where these OH groups have been replaced in a systematic manner by OMe and OAc groups. Proapoptotic activities of six embelin derivatives have been studied as single agent, or in combination with TRAIL, and their abilities to interact with XIAP have been evaluated by Surface Plasmon Biacore. Our results show that these new embelin analogs have good proapoptotic properties against selected cancer cells, often higher than the natural product itself. Further, this activity is not directly mediated by XIAP. Altogether these preliminary results demonstrate that for active embelin analogs, the two OH groups are not absolutely required for anticancer activity, opening new possibilities for the design of proapoptotic derivatives in these series.
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https://hal-univ-rennes1.archives-ouvertes.fr/hal-01147397
Contributor : Laurent Jonchère <>
Submitted on : Thursday, April 30, 2015 - 11:55:02 AM
Last modification on : Saturday, July 11, 2020 - 3:14:16 AM

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Guillaume Viault, Katragadda Suresh Babu, Fabien Gautier, Sophie Barillé-Nion, Philippe Juin, et al.. Hemisynthesis of selected embelin analogs and investigation of their proapoptotic activity against cancer cells. Medicinal Chemistry (Shāriqah (United Arab Emirates)), 2013, 9 (8), pp.1028--1034. ⟨10.2174/1573406411309080003⟩. ⟨hal-01147397⟩

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