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Merck

Celastrol inhibits Plasmodium falciparum enoyl-acyl carrier protein reductase.

Bioorganic & medicinal chemistry (2014-10-07)
Lorillee C Tallorin, Jacob D Durrant, Quynh G Nguyen, J Andrew McCammon, Michael D Burkart
RÉSUMÉ

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.

MATÉRIAUX
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Description du produit

Sigma-Aldrich
Iodoacétamide, Single use vial of 56 mg
Sigma-Aldrich
Iodoacétamide, BioUltra
Sigma-Aldrich
Iodoacétamide, ≥99% (NMR), crystalline
Sigma-Aldrich
Triclosan, 97.0-103.0% (active substance, GC)
SAFC
Iodoacétamide
USP
Triclosan, United States Pharmacopeia (USP) Reference Standard
Supelco
Triclosan, Pharmaceutical Secondary Standard; Certified Reference Material