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Bioorg Med Chem ; 25(5): 1672-1680, 2017 03 01.
Article in English | MEDLINE | ID: mdl-28162900

ABSTRACT

FIKKs are parasite-specific protein kinases with distinctive sequence motifs and their biological roles have not been completely elucidated. Here, we report the first potent Cryptosporidium FIKK (CpFIKK) inhibitor. We identified 4b as a potent (IC50=0.2nM) inhibitor of CpFIKK catalytic activity. In addition, we identified both CpCDPK1 selective as well as dually acting CpFIKK-CDPK1 inhibitors from the same structural class of compounds. We evaluated these CpFIKK inhibitors for inhibition of parasite growth in vitro. The observed effects on parasite growth did not correlate with CpFIKK inhibition, suggesting that CpFIKK may not be involved in parasite growth.


Subject(s)
Cryptosporidium/enzymology , Protein Kinase Inhibitors/chemistry , Protein Kinase Inhibitors/pharmacology , Protein Kinases/chemistry , Amino Acid Sequence , Cryptosporidium/growth & development , Drug Discovery , Humans , Sequence Homology, Amino Acid , Spectrum Analysis/methods , Structure-Activity Relationship
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