Conformational Aspects in the Design of Inhibitors for Serine Hydroxymethyltransferase (SHMT): Biphenyl, Aryl Sulfonamide, and Aryl Sulfone Motifs. Issue 57 (2nd October 2017)

• Record Type: Journal Article
• Authors: Schwertz, Geoffrey; Frei, Michelle S.; Witschel, Matthias C.; Rottmann, Matthias; Leartsakulpanich, Ubolsree; Chitnumsub, Penchit; Jaruwat, Aritsara; Ittarat, Wanwipa; Schäfer, Anja; Aponte, Raphael A.; Trapp, Nils; Mark, Kerstin; Chaiyen, Pimchai; Diederich, François
• Is Part Of: Chemistry. Volume 23:Issue 57(2017)
• Page Start: 14345
• Page End: 14357
• Publication Date: 2017-10-02
• Subjects: co-crystal structures -- conformation analysis -- drug design -- plasmodium -- serine hydroxymethyltransferase; Chemistry -- Periodicals; 540
• DOI: 10.1002/chem.201703244
• Languages: English
• ISSNs: 0947-6539

Abstract

Abstract: Malaria remains a major threat to mankind due to the perpetual emergence of resistance against marketed drugs. Twenty‐one pyrazolopyran‐based inhibitors bearing terminal biphenyl, aryl sulfonamide, or aryl sulfone motifs were synthesized and tested towards serine hydroxymethyltransferase (SHMT), a key enzyme of the folate cycle. The best ligands inhibited Plasmodium falciparum ( Pf ) and Arabidopsis thaliana ( At ) SHMT in target, as well as Pf NF54 strains in cell‐based assays in the low nanomolar range (18–56 nm ). Seven co‐crystal structures with P. vivax ( Pv ) SHMT were solved at 2.2–2.6 Å resolution. We observed an unprecedented influence of the torsion angle of ortho ‐substituted biphenyl moieties on cell‐based efficacy. The peculiar lipophilic character of the sulfonyl moiety was highlighted in the complexes with aryl sulfonamide analogues, which bind in their preferred staggered orientation. The results are discussed within the context of conformational preferences in the ligands. Abstract : Mind the conformation ! Two potent series of pyrazolopyran‐based inhibitors of the enzyme serine hydroxymethyltransferase (SHMT), bearing either terminal biphenyl, aryl sulfonamide, or aryl sulfone motif are reported. The substantial influence of the torsion angle of the biphenyl moiety on the cell‐based efficacy is discussed. Additionally, the preferred conformations of aryl sulfonamide/aryl sulfone moieties and their lipophilic character in the complexes with P. vivax SHMT were analyzed.