| Literature DB >> 25284249 |
Lorillee C Tallorin, Jacob D Durrant, Quynh G Nguyen, J Andrew McCammon, Michael D Burkart.
Abstract
Enoyl-acyl carrier protein reductase (ENR), a critical enzyme in type II fatty acid biosynthesis, is a promising target for drug discovery against hepatocyte-stage Plasmodium falciparum. In order to identify PfENR-specific inhibitors, we docked 70 FDA-approved, bioactive, and/or natural product small molecules known to inhibit the growth of whole-cell blood-stage P. falciparum into several PfENR crystallographic structures. Subsequent in vitro activity assays identified a noncompetitive low-micromolar PfENR inhibitor, celastrol, from this set of compounds.Entities:
Keywords: Celastrol; Enoyl-acyl carrier protein reductase; Malaria; Plasmodium falciparum; in silico
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Year: 2014 PMID: 25284249 PMCID: PMC4807855 DOI: 10.1016/j.bmc.2014.09.002
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641