Chemical Structure : 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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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.
| M.Wt | 360.41 | |
| Formula | C18H24N4O4 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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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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