| Literature DB >> 30451500 |
Laura Friggeri1, Tatiana Y Hargrove1, Girish Rachakonda2, Anna L Blobaum3, Paxtyn Fisher4, Gabriel Melo de Oliveira5, Cristiane França da Silva5, Maria de Nazaré C Soeiro5, W David Nes4, Craig W Lindsley3, Fernando Villalta2, F Peter Guengerich1, Galina I Lepesheva1,6.
Abstract
Sterol 14α-demethylases (CYP51) are cytochrome P450 enzymes essential for sterol biosynthesis in eukaryotes and therapeutic targets for antifungal azoles. Multiple attempts to repurpose antifungals for treatment of human infections with protozoa (Trypanosomatidae) have been undertaken, yet so far none of them have revealed sufficient efficacy. VNI and its derivative VFV are two potent experimental inhibitors of Trypanosomatidae CYP51, effective in vivo against Chagas disease, visceral leishmaniasis, and sleeping sickness and currently under consideration as antiprotozoal drug candidates. However, VNI is less potent against Leishmania and drug-resistant strains of Trypanosoma cruzi and VFV, while displaying a broader spectrum of antiprotozoal activity, and is metabolically less stable. In this work we have designed, synthesized, and characterized a set of close analogues and identified two new compounds (7 and 9) that exceed VNI/VFV in their spectra of antiprotozoal activity, microsomal stability, and pharmacokinetics (tissue distribution in particular) and, like VNI/VFV, reveal no acute toxicity.Entities:
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Year: 2018 PMID: 30451500 PMCID: PMC6467724 DOI: 10.1021/acs.jmedchem.8b01671
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446