| Literature DB >> 32575985 |
Andrew S Bell1, Zhiyong Yu1, Jennie A Hutton1, Megan H Wright2, James A Brannigan3, Daniel Paape4, Shirley M Roberts3, Charlotte L Sutherell1, Markus Ritzefeld1, Anthony J Wilkinson3, Deborah F Smith4, Robin J Leatherbarrow1, Edward W Tate1.
Abstract
The leishmaniases, caused by Leishmania species of protozoan parasites, are neglected tropical diseases with millions of cases worldwide. Current therapeutic approaches are limited by toxicity, resistance, and cost. N-Myristoyltransferase (NMT), an enzyme ubiquitous and essential in all eukaryotes, has been validated via genetic and pharmacological methods as a promising anti-leishmanial target. Here we describe a comprehensive structure-activity relationship (SAR) study of a thienopyrimidine series previously identified in a high-throughput screen against Leishmania NMT, across 68 compounds in enzyme- and cell-based assay formats. Using a chemical tagging target engagement biomarker assay, we identify the first inhibitor in this series with on-target NMT activity in leishmania parasites. Furthermore, crystal structure analyses of 12 derivatives in complex with Leishmania major NMT revealed key factors important for future structure-guided optimization delivering IMP-105 (43), a compound with modest activity against Leishmania donovani intracellular amastigotes and excellent selectivity (>660-fold) for Leishmania NMT over human NMTs.Entities:
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Year: 2020 PMID: 32575985 PMCID: PMC7383931 DOI: 10.1021/acs.jmedchem.0c00570
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446