Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/329637
Type: Artigo
Title: Novel Inhibitors Of Plasmodium Falciparum Based On 2,5-disubstituted Furans
Author: Krake
Susann H.; Martinez
Pablo David G.; McLaren
Jenna; Ryan
Eileen; Chen
Gong; White
Karen; Charman
Susan A.; Campbell
Simon; Willis
Paul; Dias
Luiz Carlos
Abstract: Phenotypic HTS campaigns with a blood stage malaria assay have been used to discover novel chemo-types for malaria treatment with potential alternative mechanisms of action compared to existing agents. N-1-(5-(3-Chloro-4-fluorophenyl)furan-2-yl)-N-3,N-3-dimethylpropane-1,3-diamine, 1 was identified as a modest inhibitor of P. falciparum NF54 (IC50 = 875 nM) with an apparent long plasma half-life after high dose oral administration to mice, although the compound later showed poor metabolic stability in liver microsomes through ring- and side chain-oxidation and N-dealkylation. We describe here the synthesis of derivatives of 1, exploring the influence of substitution patterns around the aromatic ring, variations on the alkyl chain and modifications in the core heterocycle, in order to probe potency and metabolic stability, where 4k showed a long half-life in rats. (C) 2016 Elsevier Masson SAS. All rights reserved.
Subject: Malaria
Furan
Diamines
Synthesis
Nm Inhibitors
Editor: Elsevier France-Editions Scientifiques Medicales Elsevier
Paris
Citation: European Journal Of Medicinal Chemistry . Elsevier France-editions Scientifiques Medicales Elsevier, v. 126, p. 929 - 936, 2017.
Rights: fechado
Identifier DOI: 10.1016/j.ejmech.2016.12.024
Address: http://www-sciencedirect-com.ez88.periodicos.capes.gov.br/science/article/pii/S0223523416310303?via%3Dihub
Date Issue: 2017
Appears in Collections:Unicamp - Artigos e Outros Documentos

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