Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/197471
Type: Artigo de periódico
Title: Structure-activity Relationship Of Antileishmanials Neolignan Analogues.
Author: Aveniente, Mário
Pinto, Eduardo F
Santos, Lourivaldo S
Rossi-Bergmann, Bartira
Barata, Lauro E S
Abstract: Twenty-two synthetic analogues of neolignans comprising beta-ketoethers and beta-ketosulfides were obtained from condensation reactions among beta-bromoketones and phenols or thiophenols, respectively, in basic solutions, and assayed in vitro for activity against intracellular Leishmania amazonensis and Leishmania donovani amastigotes, the causative agents of cutaneous and visceral leishmaniasis. The highest selective activity was found for compounds with sulfur bridges, whereas beta-ketosulphoxides and beta-ketosulphones had significantly less growth inhibitory activity. Compounds 2-[(4-chlorophenyl)thio]propan-1-one and 1-(3,4-dimethoxy)-2-[(4-methylphenyl)thio]propan-1-one were the most potent, inhibiting the growth parasite species by over 90% at microgram/mL, but only compound 1-(3,4-dimethoxy)-2-[(4-methylphenyl)thio]propan-1-one was selectively toxic to the parasites.
Subject: Animals
Antiprotozoal Agents
Cells, Cultured
Disease Models, Animal
Leishmania
Leishmaniasis
Lignans
Macrophages, Peritoneal
Mice
Mice, Inbred Balb C
Molecular Structure
Parasitic Sensitivity Tests
Species Specificity
Stereoisomerism
Structure-activity Relationship
Rights: fechado
Identifier DOI: 10.1016/j.bmc.2007.08.016
Address: http://www.ncbi.nlm.nih.gov/pubmed/17888668
Date Issue: 2007
Appears in Collections:Artigos e Materiais de Revistas Científicas - Unicamp

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