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- W4294990744 endingPage "1045" @default.
- W4294990744 startingPage "1029" @default.
- W4294990744 abstract "Trypanosomatidic parasitic infections in humans and animals caused by Trypanosoma brucei, Trypanosoma cruzi, and Leishmania species pose a significant health and economic burden in developing countries. There are few effective and accessible treatments for these diseases, and the existing therapies suffer from problems, such as parasite resistance and side effects. Structure-based drug design (SBDD) is one of the strategies that has been applied to discover new compounds targeting trypanosomatid-borne diseases.We review the current literature (mostly over the last 5 years, searched in the PubMed database on 11 November 2021) on the application of structure-based drug design approaches to identify new anti-trypanosomatidic compounds that interfere with a validated target biochemical pathway, the trypanosomatid folate pathway.The application of structure-based drug design approaches to perturb the trypanosomatid folate pathway has successfully provided many new inhibitors with good selectivity profiles, most of which are natural products or their derivatives or have scaffolds of known drugs. However, the inhibitory effect against the target protein(s) often does not translate to anti-parasitic activity. Further progress is hampered by our incomplete understanding of parasite biology and biochemistry, which is necessary to complement SBDD in a multiparameter optimization approach to discovering selective anti-parasitic drugs." @default.
- W4294990744 created "2022-09-09" @default.
- W4294990744 creator A5000858314 @default.
- W4294990744 creator A5011813974 @default.
- W4294990744 creator A5062698572 @default.
- W4294990744 date "2022-09-02" @default.
- W4294990744 modified "2023-09-30" @default.
- W4294990744 title "Anti-trypanosomatid structure-based drug design – lessons learned from targeting the folate pathway" @default.
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