Abstract
Carbocyclic and acyclic nucleosides possessing 2-fluoroadenine, such as 2-fluoronoraristeromycin (6) and 2-fluoro-9-[(2S,3R)-2,3,4-trihydroxy-butyl-1-yl]adenine (8), were synthesized and their inhibitory activities against human and Plasmodium falciparum recombinant SAH hydrolase were investigated.
Original language | English |
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Pages (from-to) | 5-6 |
Number of pages | 2 |
Journal | Nucleic acids research. Supplement (2001) |
Issue number | 3 |
DOIs | |
Publication status | Published - 2003 |
Externally published | Yes |
ASJC Scopus subject areas
- Medicine(all)