| Literature DB >> 28162900 |
Khan T Osman1, Juntao Ye2, Zhihao Shi3, Christina Toker2, Diogo Lovato4, Rajiv S Jumani5, William Zuercher6, Christopher D Huston5, Aled M Edwards4, Mark Lautens2, Vijayaratnam Santhakumar7, Raymond Hui4.
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.Keywords: Cryptosporidium; FIKK Kinase inhibitor; Kinase inhibitor
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Year: 2017 PMID: 28162900 DOI: 10.1016/j.bmc.2017.01.036
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641