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Dicyclic and Tricyclic Diaminopyrimidine Derivatives as Potent Inhibitors of Cryptosporidium parvum Dihydrofolate Reductase: Structure-Activity and Structure-Selectivity Correlations

A structurally diverse library of 93 lipophilic di- and tricyclic diaminopyrimidine derivatives was tested for the ability to inhibit recombinant dihydrofolate reductase (DHFR) cloned from human and bovine isolates of Cryptosporidium parvum (J. R. Vásquez et al., Mol. Biochem. Parasitol. 79:153–165,...

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Detaylı Bibliyografya
Asıl Yazarlar: Nelson, Richard G., Rosowsky, Andre
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Society for Microbiology 2001
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC90829/
https://ncbi.nlm.nih.gov/pubmed/11709300
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1128/AAC.45.12.3293-3303.2001
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