| Cat. No. |
Product Name |
Information |
| PC-45158 |
Doramectin
Antibiotic
|
Doramectin is a derivative of ivermectin that approved for the treatment of parasites, is an active compound against S.mansoni in an NMRI mouse infection model. |
| PC-25082 |
Piperaquine tetraphosphate tetrahydrate
Antimalarial
|
Piperaquine tetraphosphate tetrahydrate is a bisquinoline antimalarial agent. |
| PC-25081 |
Piperaquine phosphate
Antimalarial
|
Piperaquine phosphate is a bisquinoline antimalarial agent. |
| PC-25080 |
Piperaquine
Antimalarial
|
Piperaquine is a bisquinoline antimalarial agent. |
| 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-24979 |
DMU759
TcKRS1 inhibitor
|
DMU759 is a specific inhibitor of T. cruzi lysyl-tRNA synthetase 1 (TcKRS1) with IC50 of 15 nM, demonstrates potent activity against T. cruzi (Sylvio X10/7A1strain) with EC50 of 14 nM. |
| PC-24978 |
DMU371
TcKRS1 inhibitor
|
DMU371 is a specific inhibitor of T. cruzi lysyl-tRNA synthetase 1 (TcKRS1) with IC50 of 185 nM, demonstrates potent activity against T. cruzi (Sylvio X10/7A1strain) with EC50 of 63 nM. |
| PC-24976 |
PfPK6 inhibitor compound 12
PfPK6 inhibitor
|
PfPK6 inhibitor Compound 12 is a potent, selective type II kinase inhibitor of Plasmodium protein kinase 6 (PfPK6) with IC50 of 301 nM, displays nanomolar activity against P. falciparum asexual blood stages with EC50 of 0.1 uM (P. falciparum Dd2 strain). |
| PC-24890 |
AN3661
PfCPSF3 inhibitor
|
AN3661 is a specific small molecule inhibitor of Toxoplasma gondii CPSF3 (TgCPSF3), demonstrates potent activity against Toxoplasma gondii in vitro with IC50 of 0.9 uM. |
| PC-24812 |
Ivermectin
CAS 70288-86-7
|
Ivermectin (MK-933) is a broad-spectrum anti-parasite agent, is a specific inhibitor ofimportin α/β-mediated nuclear import with potent antiviral activity towards both HIV-1 and DENV, also is a positive allosteric effector of P2X4 and α7 neuronal nicotinic acetylcholine receptor (nAChRs), also inhibits bovine herpesvirus1 (BoHV-1) replication and inhibits BoHV-1 DNA polymerase nuclear import. |
| PC-24762 |
Endochin
T. gondii bc1 inhibitor
|
Endochin is an antimalarial agent, inhibits T. gondii growth in vitro (IC50=0.003 nM), inhibits inhibited T.gondii cytochrome c reduction with IC50 of 8.2 nM. |
| PC-24761 |
ELQ-271
T. gondii bc1 inhibitor
|
ELQ-271 is a potent, orally bioavailable inhibitor of T. gondii growth in vitro (IC50=0.1 nM) and is effective against acute and latent toxoplasmosis in mice, inhibits cytochrome c reduction by the T. gondii cytochrome bc(1) complex. |
