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Purfalcamine

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. Purfalcamine has antimalarial activity and causes malaria parasites developmental arrest at the schizont stage[1][2].

Product Specifications

CAS Number

[1038620-68-6]

Product Name Alternative

Y-39992

UNSPSC

12352005

Target

Parasite

Type

Reference compound

Related Pathways

Anti-infection

Applications

COVID-19-immunoregulation

Field of Research

Infection

Assay Protocol

https://www.medchemexpress.com/purfalcamine.html

Purity

99.44

Solubility

DMSO : 12.5 mg/mL (ultrasonic)

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

Molecular Formula

C29H33FN8O

Molecular Weight

528.62

References & Citations

Plasmodium falciparumToxoplasma gondii

Shipping Conditions

Room Temperature

Storage Conditions

-20°C, 3 years; 4°C, 2 years (Powder)

Scientific Category

Reference compound1

Clinical Information

No Development Reported

Isoform

Plasmodium; Toxoplasma

Available Sizes

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