ABSTRACT
The nematocidal in vitro activity of three natural perotetins (phenolic bisbibenzyiethers) and eleven diphenyl ethers used as synthetic precursors has been assayed using two different experimental models, Caenorhabditis elegans and Nippostrongylus brasiliensis. Nine compounds showed some activity against C. elegans and nine against N. brasiliensis. For the former model, three compounds displayed an activity similar to that of the standards, whereas for N. brasiliensis none of the tested compounds was as active as the standards. From the in vitro results, five compounds (3, 4, 8, 9, 13) could be selected as lead compounds to continue the search for improved activity.
Subject(s)
Antinematodal Agents/pharmacology , Bryopsida/chemistry , Phenols/pharmacology , Animals , Anthelmintics/chemical synthesis , Anthelmintics/pharmacology , Antinematodal Agents/chemical synthesis , Antinematodal Agents/isolation & purification , Caenorhabditis elegans/drug effects , Lethal Dose 50 , Nippostrongylus/drug effects , Phenols/chemical synthesis , Phenols/isolation & purification , Structure-Activity RelationshipABSTRACT
A series of compounds bearing an endocyclic -N-O- moiety with potential antimalarial activity based on simple derivatives of the tropolone purpurogallin was prepared by means of a hetero Diels-Alder reaction using nitrosobenzene as a dienophile. The rationale behind the design of these compounds is presented, together with the synthetic route to derivatives bearing aromatic and aliphatic esters of the C4'-position hydroxyl group of the purpurogallin framework, as well as biological data obtained from in vitro assays against Plasmodium falciparum and Trypanosoma cruzi. Several of the new compounds have activities in the 3-9 microM range, and provide leads for the development of a novel class of antiparasitic drugs with improved biological and pharmacological properties.
