Issue 49, 2017, Issue in Progress

Heat shock protein 90 and serine/threonine kinase B-Raf inhibitors have overlapping chemical space

Abstract

Heat shock protein 90 (Hsp90) and B-Raf are validated targets for anticancer drug discovery. Although there is strong evidence that concomitant inhibition of Hsp90 and B-Raf may provide significant therapeutic benefits, molecules endowed with dual activity against the two targets have not been reported. For the first time, we show that Hsp90 and B-Raf inhibitors have overlapping chemical space and we disclose the first-in-class dual inhibitors. The compounds were identified through a computational strategy especially devised for detecting ligands with dual-target activity. Although the two targets had only remote binding site similarity, we were able to identify dual inhibitors with well-balanced in vitro potencies and relatively low molecular weight. Remarkably, they also inhibited the V600E mutant form of B-Raf with similar potency. This study provides the first direct proof that designing dual ligands of Hsp90 and a kinase is possible, thus opening the way to new interesting possibilities in drug discovery.

Graphical abstract: Heat shock protein 90 and serine/threonine kinase B-Raf inhibitors have overlapping chemical space

Supplementary files

Article information

Article type
Paper
Submitted
25 May 2017
Accepted
10 Jun 2017
First published
15 Jun 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 31069-31074

Heat shock protein 90 and serine/threonine kinase B-Raf inhibitors have overlapping chemical space

A. Anighoro, L. Pinzi, G. Marverti, J. Bajorath and G. Rastelli, RSC Adv., 2017, 7, 31069 DOI: 10.1039/C7RA05889F

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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