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- W2594312336 abstract "ABSTRACT Schistosomiasis, a major neglected tropical disease, affects more than 250 million people worldwide. Treatment of schistosomiasis has relied on the anthelmintic drug praziquantel (PZQ) for more than a generation. PZQ is the drug of choice for the treatment of schistosomiasis; it is effective against all major forms of schistosomiasis, although it is less active against juvenile than mature parasites. A pyrazino-isoquinoline derivative, PZQ is not considered to be toxic and generally causes few or transient, mild side effects. Increasingly, mass drug administration targeting populations in sub-Saharan Africa where schistosomiasis is endemic has led to the appearance of reduced efficacy of PZQ, which portends the selection of drug-resistant forms of these pathogens. The synthesis of improved derivatives of PZQ is attracting attention, e.g., in the (i) synthesis of drug analogues, (ii) rational design of pharmacophores, and (iii) discovery of new compounds from large-scale screening programs. This article reviews reports from the 1970s to the present on the metabolism and mechanism of action of PZQ and its derivatives against schistosomes." @default.
- W2594312336 created "2017-03-16" @default.
- W2594312336 creator A5007882171 @default.
- W2594312336 creator A5028251855 @default.
- W2594312336 creator A5030729996 @default.
- W2594312336 creator A5049513875 @default.
- W2594312336 creator A5054091339 @default.
- W2594312336 creator A5058709882 @default.
- W2594312336 date "2017-05-01" @default.
- W2594312336 modified "2023-10-16" @default.
- W2594312336 title "Praziquantel for Schistosomiasis: Single-Drug Metabolism Revisited, Mode of Action, and Resistance" @default.
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