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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,...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Nelson, Richard G., Rosowsky, Andre
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: American Society for Microbiology 2001
Gaiak:
Sarrera elektronikoa: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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