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首页-小分子抑制剂&激动剂-Antibiotics and Antivirals-Parasite

Request The Product List ofParasite Parasite

Cat. No. Product Name Information
PC-27569

WHZ-04

Pf20S inhibitor

WHZ-04 is a potent, selective P. falciparum 20S proteasome (Pf20S) inhibitor with IC50 of 20.8 nM for Pf20S β5, has 68-fold and 4.8-fold selectivity over β5c and β5i, shows antimalarial EC50 of 8.4 nM against Pf 3D7.
PC-27443

RUPB-61

PfPKG inhibitor

RUPB-61 is a potent, selective and orally bioavailable inhibitor of Plasmodium falciparum cGMP-dependent protein kinase (PfPKG) with IC50 of 13 nM, EC50 of 50 uM against multi-drug resistant P. falciparum lab strain 3D7, blocks sporozoite infection of the liver.
PC-27209

CWHM-1008

Antimalarial

CWHM-1008 is a potent, orally efficacious antimalarial agent with EC50 values of 46 nM and 21 nM against drug sensitive Plasmodium falciparum 3D7 and drug resistant Dd2 strains, respectively.
PC-27175

UCB-9721

TgMyoA inhibitor

UCB-9721 is a potent inhibitor of T. gondii MyoA (TgMyoA) with IC50 of 31 nM, a class XIV myosin motor of apicomplexan parasites, inhibits TgMyoA actin-activated ATPase activity.
PC-26128

Cruzidione

T. cruzi inhibitor

Cruzidione is a potent anti-T. cruzi activity and anti-Chagas compound with anti-trypanosomal activity with IC50 of 3.65 uM.
PC-25293

LXE408

Kinetoplastid proteasome inhibitor

Galeflaprit (LXE408) is a potent, selective inhibitor of the kinetoplastid proteasome with IC50 of 0.04 uM (L. donovani proteasome), inhibits L. donovani amastigote proliferation within primary mouse macrophages (IC50=0.04 uM).
PC-25200

BKI-1708

CpCDPK1 inhibitor

BKI-1708 is a highly potent, specific Cryptosporidium calcium-dependent protein kinase 1 (CDPK1) inhibitor with IC50 of 0.7 nM (CpCDPK1, C. parvum CDPK1) and EC50 of 0.4 uM against C. parvum parasites in Nanoluciferase assays.
PC-25005

ZY-19489

Antimalarial

Sutidiazine (Zintrodiazine, ZY-19489, MMV 253, AZ-13721412) is a novel antimalarial triaminopyrimidine compound with IC50 of 9 nM against sexual blood stage of Plasmodium falciparum (Pf).
PC-24759

BKI-1748

CDPK1 inhibitor

BKI-1748 a small molecule bumped kinase inhibitor targeting calcium dependent protein kinase 1 (CDPK1), inhibits TgCDPK1 and NcCDPK1 enzyme activities at low nM-concentrations, inhibits proliferation of apicomplexan parasites with EC50 of 165 nM for N. caninum and 43 nM for T. gondii.
PC-23131

EDI048

Cryptosporidium PI4K inhibitor

EDI048 (EDI-048) is a specific, ATP-competitive, gastrointestinal-targeted Cryptosporidium PI(4)K (CpPI(4)K) inhibitor with IC50 of 4 nM, >300-fold with human orthologue HsPI(4)K, demonstrates in vitro anti-Cryptosporidium activity (Cp CPE, EC50=52 nM).
PC-22969

UCT594

Pf PI4K inhibitor

UCT594 is a highly potent, selective Plasmodium phosphatidylinositol 4-kinase (PI4K) inhibitor, inhibits the P. vivax PI4K enzyme with IC50 of 24 nM, >200-fold selective over human PI4Kβ ortholog.
PC-22800

SW584

Pf20Sβ5 inhibitor

SW584 is a potent, species-selective, orally active inhibitor of P. falciparum proteasome β5 active site (Pf20Sβ5) with IC50 of 5.8 nM, shows antimalarial activity with EC50 of 3 nM (Pf3D7 and PfDd2).

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