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Chem Biodivers ; 21(5): e202400491, 2024 May.
Article in English | MEDLINE | ID: mdl-38470945

ABSTRACT

We have evaluated eight p-coumaric acid prenylated derivatives in vitro for their antileishmanial activity against Leishmania amazonensis promastigotes and their antischistosomal activity against Schistosoma mansoni adult worms. Compound 7 ((E)-3,4-diprenyl-4-isoprenyloxycinnamic alcohol) was the most active against L. amazonensis (IC50=45.92 µM) and S. mansoni (IC50=64.25 µM). Data indicated that the number of prenyl groups, the presence of hydroxyl at C9, and a single bond between C7 and C8 are important structural features for the antileishmanial activity of p-coumaric acid prenylated derivatives.


Subject(s)
Antiprotozoal Agents , Coumaric Acids , Leishmania , Parasitic Sensitivity Tests , Schistosoma mansoni , Animals , Schistosoma mansoni/drug effects , Coumaric Acids/pharmacology , Coumaric Acids/chemistry , Leishmania/drug effects , Antiprotozoal Agents/pharmacology , Antiprotozoal Agents/chemistry , Antiprotozoal Agents/chemical synthesis , Structure-Activity Relationship , Prenylation , Propionates/pharmacology , Propionates/chemistry , Molecular Structure , Schistosomicides/pharmacology , Schistosomicides/chemistry , Schistosomicides/chemical synthesis , Dose-Response Relationship, Drug
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