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Chemical structure of Purfalcamine

GC61222

Purfalcamine

Also known as [4-[[2-[(4-aminocyclohexyl)amino]-9-(3-fluorophenyl)purin-6-yl]amino]phenyl]-piperidin-1-ylmethanone

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

ChemicalCAS1038620-68-6MW528.62FormulaC29H33FN8O
CAS number
1038620-68-6
Molecular weight
528.62
Formula
C29H33FN8O
Solubility
DMSO ： 12·5 mg/mL (23·65 mM; Need ultrasonic)
InChIKey
KRCOMOOXOZSNAJ-UHFFFAOYSA-N
Catalogue number
GC61222
Brand
GLPBIO
Computed properties PubChem CID 24762166 · XLogP 4.7 · TPSA 114 Ų · H-bond donors 3
XLogP
4.7
TPSA
114 Ų
H-bond donors
3
H-bond acceptors
8
Rotatable bonds
6
Heavy atoms
39

SMILES C1CCN(CC1)C(=O)C2=CC=C(C=C2)NC3=C4C(=NC(=N3)NC5CCC(CC5)N)N(C=N4)C6=CC(=CC=C6)F

Computed descriptors from PubChem (CID 24762166), public domain. Identity cross-checked against the supplier's molecular formula and weight — verify before use.

Ordering in Israel

Lead time
Ships from the manufacturer to your lab in 8–14 business days; customs and cold chain handled by LABO Scientific.
Pricing
Quoted in ILS, excl. VAT. Add the item to your quote and we confirm the final price, usually the same business day.
Documents
Lot certificate of analysis and manufacturer SDS are emailed with your order confirmation.
Who we serve
Universities, hospitals and biotech companies across Israel. Research use only — not for diagnostic or therapeutic use.