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PfDHFR inhibitor P218

Chemical Structure : PfDHFR inhibitor P218

CAS No.: 1142407-81-5

PfDHFR inhibitor P218

Catalog No.: PC-26679Not For Human Use, Lab Use Only.

PfDHFR inhibitor P218 is a highly potent inhibitor of Plasmodium falciparum dihydrofolate reductase (PfDHFR) with Ki of 0.54 nM for quadruple mutant P. falciparum DHFR, inhibits wild-type P. falciparum (TM4) and quadruple mutant P. falciparum (V1/S) with IC50 of 4.6 nM and 56 nM.

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Purity & Documentation Purity: >98% (HPLC)

Biological Activity

PfDHFR inhibitor P218 is a highly potent inhibitor of Plasmodium falciparum dihydrofolate reductase (PfDHFR) with Ki of 0.54 nM for quadruple mutant P. falciparum DHFR, inhibits wild-type P. falciparum (TM4) and quadruple mutant P. falciparum (V1/S) with IC50 of 4.6 nM and 56 nM.

Physicochemical Properties

M.Wt 360.41
Formula C18H24N4O4
Appearance Solid
CAS No.
Storage
Solide Powder
-20°C 12 Months; 4°C 6 Months
In Solvent
-80°C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

3-(2-(3-((2,4-diamino-6-ethylpyrimidin-5-yl)oxy)propoxy)phenyl)propanoic acid

References

1. Decharuangsilp S, et al. Eur J Med Chem. 2026 Apr 19;313:118863.

2. Yuthavong Y, et al. Proc Natl Acad Sci U S A. 2012 Oct 16;109(42):16823-8.

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