Purfalcamine is an orally active, selective Plasmodium falciparum calcium-dependent protein kinase 1 (PfCDPK1) inhibitor with an IC50 of 17 nM and an EC50 of 230 nM, exhibiting antimalarial activity by inducing developmental arrest of malaria parasites at the schizont stage[1][2].
Molecular Weight:
528.62
CAS Number:
[1038620-68-6]
Formula:
C29H33FN8O
Target:
Parasite|||Others
T38269
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