| Literature DB >> 25785478 |
Matthias C Witschel1, Matthias Rottmann2,3, Anatol Schwab4, Ubolsree Leartsakulpanich5, Penchit Chitnumsub5, Michael Seet4, Sandro Tonazzi4, Geoffrey Schwertz4, Frank Stelzer1, Thomas Mietzner1, Case McNamara6, Frank Thater1, Céline Freymond2,3, Aritsara Jaruwat5, Chatchadaporn Pinthong7, Pinpunya Riangrungroj5, Mouhssin Oufir8, Matthias Hamburger8, Pascal Mäser2,3, Laura M Sanz-Alonso9, Susan Charman10, Sergio Wittlin2,3, Yongyuth Yuthavong5, Pimchai Chaiyen7, François Diederich4.
Abstract
Several of the enzymes related to the folate cycle are well-known for their role as clinically validated antimalarial targets. Nevertheless for serine hydroxymethyltransferase (SHMT), one of the key enzymes of this cycle, efficient inhibitors have not been described so far. On the basis of plant SHMT inhibitors from an herbicide optimization program, highly potent inhibitors of Plasmodium falciparum (Pf) and Plasmodium vivax (Pv) SHMT with a pyrazolopyran core structure were identified. Cocrystal structures of potent inhibitors with PvSHMT were solved at 2.6 Å resolution. These ligands showed activity (IC50/EC50 values) in the nanomolar range against purified PfSHMT, blood-stage Pf, and liver-stage P. berghei (Pb) cells and a high selectivity when assayed against mammalian cell lines. Pharmacokinetic limitations are the most plausible explanation for lack of significant activity of the inhibitors in the in vivo Pb mouse malaria model.Entities:
Mesh:
Substances:
Year: 2015 PMID: 25785478 DOI: 10.1021/jm501987h
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446