| Cat. No. |
Product Name |
Information |
| PC-45379 |
Mebendazole
|
Mebendazole is a highly effective, broad-spectrum antihelmintic by selectively inhibiting the synthesis of microtubules in parasitic worms, and by destroying extant cytoplasmic microtubes in their intestinal cells.. |
| PC-23658 |
SAL-0010042
P. falciparum PDEβ inhibitor
|
SAL-0010042 is a fast-acting and potent Plasmodium falciparum PDEβ inhibitor with IC50 of 10.8 nM for cGMP hydrolysis in crude gametocyte membrane preparations, and EC50 of 142 nM for 3D7 blood stage. |
| PC-23657 |
SAL-0010003
P. falciparum PDEβ inhibitor
|
SAL-0010003 is a fast-acting and potent Plasmodium falciparum PDEβ inhibitor with IC50 of 17.3 nM for cGMP hydrolysis in crude gametocyte membrane preparations, and EC50 of 327 nM for 3D7 blood stage. |
| PC-23626 |
TCDMC-143160
TcTDH inhibitor
|
TCDMC-143160 is a specific inhibitor of T. cruzi L-threonine dehydrogrenase (TcTDH) with IC50 of 3.5 uM, inhibits the threonine degradation pathway and interferes with parasite growth and viability. |
| PC-23600 |
ML901
PfYRS inhibitor
|
ML901 is a potent, specific inhibitor of P. falciparum tyrosine tRNA synthetase (PfYRS, PfTyrRS), shows potent activity against P. falciparum with IC50 of 2.0 nM. |
| PC-23599 |
ML471
PfYRS inhibitor
|
ML471 is a potent, selective reaction hijacking inhibitor of P.falciparum tyrosine tRNA synthetase (PfTyrRS, PfYRS), inhibits growth of asexual blood stage P. falciparum (3D7 strain) in a 72-h exposure assay with IC50 of 2.8 nM. |
| PC-23461 |
VCC234718
Mtb GuaB2 inhibitor
|
VCC234718 isa potent, specific small molecule inhibitor of Mtb inosine-5′-monophosphate dehydrogenase (IMPDH) GuaB2 with Ki of 100 nM, shows growth inhibitory activity against Mycobacterium tuberculosis (Mtb H37Rv, MIC90=2 uM). |
| PC-23310 |
Jaspamycin
TbPKA inhibitor, MTA3 inhibitor
|
Jaspamycin (7-CN-7-C-Ino) is a potent activator of Trypanosoma brucei PKA (TbPKA), binding to the R site (PKAR) with EC50 of 6.5 nM and Kd of 8 nM in Trypanosoma brucei, also inhibits hepatocellular carcinoma progression via trageting metastasis-associated protein 3 (MTA3). |
| PC-23296 |
JCP174
TgPPT1 inhibitor
|
JCP174 is a small molecule inhibitor of Toxoplasma gondii palmitoyl-protein thioesterase-1 (TgPPT1), enhances Toxoplasma host-cell invasion, triggers secretion of invasion-associated organelles, increases motility and enhances the invasive capacity of tachyzoites. |
| PC-23278 |
Artemisinin
PfPI3K inhibitor
|
Artemisinin (Qinghaosu) is a sesquiterpene lactone, an anti-malarial agent isolated from the aerial parts of Artemisia annua L., potently inhibits PfPI3K. |
| PC-23277 |
PfCLK3 inhibitor 4
PfCLK3 inhibitor
|
PfCLK3 inhibitor 4 is a potent, covalent inhibitor of Plasmodium falciparum CLK3 kinase (PfCLK3) with pIC50 of 8.02, covalently targets of PfCLK3 cys368, exhibits parasiticidal activity in P. falciparum 3D7 cell line with pEC50 of 7.1. |
| PC-23268 |
DDD508
CpKRS inhibitor
|
DDD508 is a potent, selective Cryptosporidium lysyl-tRNA synthetase (CpKRS) inhibitor with IC50 of 1.7 uM, and C. parvum EC50 of 0.13 uM, shows anti-cryptosporidials activity. |
