Design and Synthesis of Metabolically Stable tRNA Synthetase Inhibitors Derived from Cladosporin. (4th February 2019)

• Record Type: Journal Article
• Authors: Rusch, Marion; Thevenon, Arnaud; Hoepfner, Dominic; Aust, Thomas; Studer, Christian; Patoor, Maude; Rollin, Patrick; Livendahl, Madeleine; Ranieri, Beatrice; Schmitt, Esther; Spanka, Carsten; Gademann, Karl; Bouchez, Laure C.
• Is Part Of: Chembiochem. Volume 20:Number 5(2019)
• Page Start: 644
• Page End: 649
• Publication Date: 2019-02-04
• Subjects: antimalarial agents -- drug discovery -- inhibitors -- natural products -- structure–activity relationships; Biochemistry -- Periodicals; Molecular biology -- Periodicals; Pharmaceutical chemistry -- Periodicals; 572
• DOI: 10.1002/cbic.201800587
• Languages: English
• ISSNs: 1439-4227

Abstract

Abstract: Selective and specific inhibitors of Plasmodium falciparum lysyl‐tRNA synthetase represent promising therapeutic antimalarial avenues. Cladosporin was identified as a potent P. falciparum lysyl‐tRNA synthetase inhibitor, with an activity against parasite lysyl‐tRNA synthetase >100‐fold more potent than that of the activity registered against the human enzyme. Despite its compelling activity, cladosporin exhibits poor oral bioavailability; a critical requirement for antimalarial drugs. Thus, the quest to develop metabolically stable cladosporin‐derived analogues, while retaining similar selectivity and potency to that of the natural compound, has begun. Chemogenomic profiling of a designed library allowed an entirely innovative structure–activity relationship study to be initiated; this shed light on structural evidence of a privileged scaffold with a unique activity against tRNA synthetases. Abstract : Ring in the changes : Selective and specific inhibitors of Plasmodium falciparum tRNA synthetases represent promising therapeutic antimalarial avenues. Chemogenomic profiling of a focused library allowed the identification of a simplified cladosporin analogue, comprising an improved potency, a superior metabolic stability to that of its natural parent, and retaining its selectivity towards the human enzyme.