Fig. 1 · Structure

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Purfalcamine

PfCDPK1 Inhibitor

Purfalcamine is a selective inhibitor of Plasmodium falciparum calcium-dependent protein kinase 1 (PfCDPK1), exhibiting an IC50 of 17 nM and an EC50 of 230 nM. It demonstrates potent antimalarial activity by inducing developmental arrest of malaria parasites at the schizont stage. This compound serves as a valuable tool for investigating the role of PfCDPK1 in malaria pathogenesis and development, offering insights into potential therapeutic strategies against malaria.

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Specifications

Manufacturer Adooq Bioscience
Actions Inhibitor
CAS Number 1038620-68-6
Applications PfCDPK1 Inhibitor
Formula C29H33FN8O
Molecular Weight 528.62
SMILES
O=C(C1=CC=C(NC2=C3N=CN(C4=CC=CC(F)=C4)C3=NC(N[C@H]5CC[C@H](N)CC5)=N2)C=C1)N6CCCCC6

Storage & Solubility

In Vitro Solubility

Reported Solubility

No reported solubility data are available for this product.

Preparing Stock Solutions

Stock preparation is unavailable for this product molecular weight.

Calculated stock concentrations do not establish solvent solubility. Refer to the reported solubility data for experimental guidance.

Storage

Store powder at -20°C, keep desiccated.
In powder form, the chemical is stable for 36 months.
In solution, store at -20°C and use within 1 month to prevent loss of potency. Aliquot to avoid multiple freeze/thaw cycles.

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