Abstract
The repertory of drugs to fight protozoal diseases such as malaria, Chagas' disease, leishmaniasis, and African trypanosomiasis is woefully inadequate. Now, genome sequencing and structural genomics projects are quickly elucidating new drug targets, providing incredible opportunities for medicinal chemists. Here, we illustrate the power of structure-based drug design in this process by our efforts to selectively block trypanosomal glycolysis.
Original language | English |
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Pages (from-to) | 843-848 |
Number of pages | 6 |
Journal | Journal of the Brazilian Chemical Society |
Volume | 13 |
Issue number | 6 |
DOIs | |
State | Published - 2002 |
Keywords
- African trypanosomiasis
- Chagas' disease
- Drug design
- GAPDH
- Leishmaniasis
- Malaria