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Cat. No. Product Name Information
PC-21553

TDI-8304

Pf20S inhibitor

TDI-8304 is a highly selective, macrocyclic peptide inhibitor of malaria parasite Plasmodium falciparum proteasome (Pf20S) with IC50 of 0.06 uM, shows high potency against P. falciparum strain Pf 3D7 (EC50=0.009 uM).
PC-21022

OSM-S-106

PfAsnRS inhibitor

OSM-S-106 is a reaction hijacking inhibitor of Plasmodium falciparum asparagine tRNA synthetase (PfAsnRS), inhibits the 3D7 line of P. falciparum with IC50 of 58 nM.
PC-20446

Nemacol-1

VAChT inhibitor

Nemacol-1 is a small molecule inhibitor of C. elegans vesicular acetylcholine transporter (VAChT), demonstrates nematode-selective activity (C. elegans, EC50=7.1 uM).
PC-20297

P4Q-391

P.f Cyt bc1 inhibitor

P4Q-391 is an antimalarial agent with selective inhibition of the parasite's coenzyme Q cycle, inhibits mitochondrial cytochrome bc1 complex (Cyt bc1).
PC-20296

ELQ-300

P.f Cyt bc1 inhibitor

ELQ-300 (ELQ300) is a potent, selective inhibitor of P. falciparummitochondrial cytochrome bc1 complex with IC50 of 0.56 nM.
PC-20295

ELQ-331

P.f Cyt bc1 inhibitor

ELQ-331 (ELQ331) is an alkoxycarbonate prodrug of antimalarial compound ELQ-300 (P. falciparum cytochrome bc1 complex inhibitor), shows P. falciparum IC50 of 6 nM.
PC-20294

GSK932121

P.f Cyt bc1 inhibitor

GSK932121 is a potent, selective inhibitor of P. falciparum cytochrome bc1 with IC50 of 7 nM, binds to Qi site of cytochrome bc1 and shows potent antimalarial activity in vitro and in vivo.
PC-20293

GW844520

P.f Cyt bc1 inhibitor

GW844520 is a potent, selective inhibitor of P. falciparum cytochrome bc1 with IC50 of 2 nM, binds to Qi site of cytochrome bc1 and shows potent antimalarial activity.
PC-20289

WJM228

P.f Cyt bc1 inhibitor

WJM228 (WJM-228) is a potent selective inhibitor of P. falciparum cytochrome bc1, targets the Qo site of cytochrome b (cyt b), shows potent parasite activity against P. falciparum 3D7 with EC50 of 19 nM.
PC-20266

Genz-667348

Pf DHODH inhibitor

Genz-667348 (Genz667348) is a potent, selective P. falciparum DHODH inhibitor with IC50 of 22, 14 and 42 nM for PfDHODH, PbDHODH and PvDHODH, respectively.
PC-20265

DSM502

Pf DHODH inhibitor

DSM502 (DSM 502) is a potent, selective inhibitor of P. falciparum and P. vivax DHODH with IC50 of 20 and 14 nM, respectively.
PC-20262

DSM267

DHODH inhibitor

DSM267 (DSM 267) is a potent, highly selective, long-duration and orally bioavailable malaria DHODH inhibitor.

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