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Cat. No. Product Name Information
PC-38663

MMV665916

PfFT inhibitor

MMV665916 is potential antimalarial agent targeting the P. falciparum farnesyltransferase (PfFT), shows remarkable growth inhibition with EC50 value of 0.4 uM.
PC-38540

Soporidine

Soporidine is a small-molecule antagonist of germination of the parasitic plant Striga hermonthica, specifically inhibits S. hermonthica strigolactone receptor and inhibits the parasite germination, disrupting the Striga lifecycle.
PC-38537

NCGC00262650

AMA1-RON2 inhibitor

NCGC00262650 is a small molecule merozoite invasion inhibitor inhibitor of parasite AMA1-RON2 interaction, blocks entry of merozoites into RBCs with IC50 of 9.8 uM.
PC-38416

MMV688533

Antimalarial

MMV688533 is a potent antimalarial compound that displays fast parasite clearance in vitro and is not cross-resistant with known antimalarials, MMV688533 is highly potent against multiple P. falciparum strains with IC50 values in low nanomolar range (P. falciparum 3D7, IC50=1.9 nM).
PC-38402

Mivorilaner

Parasiticidal agent

Mivorilaner is a parasiticidal dihydroisoxazole compound.
PC-38367

Modoflaner

Antiparasitic agent

Modoflaner is an antiparasitic agent.
PC-38359

Fanotaprim

TgDHFR inhibitor

Fanotaprim (VYR-006) is a potent, selective Toxoplasma gondii DHFR (TgDHFR) inhibitor with IC50 of 1.6 nM, 200-fold selectivity over human DHFR (hDHFR), shows anti-parasiticidal activity in vitro and in vivo.
PC-73100

MMV675968

Antifungal agent

MMV675968 is a potent, small molecule inhibitor of Toxoplasma gondii (T. gondii) with IC50 of 0.02 uM, via the pathogen box.
PC-72859

PDE-I2

Anti-malaria

PDE-I2 is a potent and selective inhibitor of malaria proliferation with Pf IC50 of 18 nM.
PC-72540

MMV084978

PfAcAS inhibitor

MMV084978 (MMV 084978) is an antiplasmodial drug-like compound tageting Plasmodium falciparum acetyl-coenzyme A synthetase (PfAcAS), directly and selectively inhibit PfAcAS activity in vitro with IC50 of 370 nM.
PC-72539

MMV019721

PfAcAS inhibitor

MMV019721 (MMV019721) is an antiplasmodial drug-like compound tageting Plasmodium falciparum acetyl-coenzyme A synthetase (PfAcAS), directly and selectively inhibit PfAcAS activity in vitro with IC50 of 73 nM.
PC-72407

CTN1122

L-CK1.2 inhibitor

CTN1122 (CTN-1122) is a potent, selective Leishmaniacasein kinase 1 isoform 2 (CK1.2, L-CK1.2) with IC50 of 0.72 uM (LmCK1) and 0.8 uM (amastigotes L. major), antileishmanial compound.

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