Identification of Inhibitors of Cholesterol Transport Proteins Through the Synthesis of a Diverse, Sterol‐Inspired Compound Collection. Issue 51 (16th November 2021)

• Record Type: Journal Article
• Authors: Whitmarsh‐Everiss, Thomas; Olsen, Asger Hegelund; Laraia, Luca
• Is Part Of: Angewandte Chemie international edition. Volume 60:Issue 51(2021)
• Page Start: 26755
• Page End: 26761
• Publication Date: 2021-11-16
• Subjects: cholesterol-transport proteins -- inhibitors -- library synthesis -- natural products; Chemistry -- Periodicals; 540
• DOI: 10.1002/anie.202111639
• Languages: English
• ISSNs: 1433-7851

Abstract

Abstract: Cholesterol transport proteins regulate a vast array of cellular processes including lipid metabolism, vesicular and non‐vesicular trafficking, organelle contact sites, and autophagy. Despite their undoubted importance, the identification of selective modulators of this class of proteins has been challenging due to the structural similarities in the cholesterol‐binding site. Herein we report a general strategy for the identification of selective inhibitors of cholesterol transport proteins via the synthesis of a diverse sterol‐inspired compound collection. Fusion of a primary sterol fragment to an array of secondary privileged scaffolds led to the identification of potent and selective inhibitors of the cholesterol transport protein Aster‐C, which displayed a surprising preference for the unnatural‐sterol AB‐ring stereochemistry and new inhibitors of Aster‐A. We propose that this strategy can and should be applied to any therapeutically relevant sterol‐binding protein. Abstract : A general strategy for the identification of selective cholesterol transport protein inhibitors through the synthesis of a diverse sterol‐inspired compound collection is presented. Fusion of a primary sterol scaffold to diverse secondary natural product‐derived scaffolds afforded hits against all of the Aster family of cholesterol transport proteins and selective inhibitors of Aster‐C.