| Cat. No. |
Product Name |
Information |
| PC-22542 |
MMV006833
PfSTART1 inhibitor
|
MMV006833 (M-833) is a small molecule inhibitor of PfSTART1 with EC50 of 1.1 uM for Pf 3D7, binds to PfSTART1(WT) with KD of 42 nM, inhibits ring-stage development of Plasmodium falciparum, prevents PfSTART1 from expanding the vacuole membrane encasing the parasite after red blood cell invasion, thereby blocking parasite growth. |
| PC-22515 |
ELQ-672
Antiparasite
|
ELQ-672 is a endochin-like quinolone compound with potent antibabesial activity with IC50 of 57 nM against B. duncani in human erythrocytes. |
| PC-22514 |
ELQ-598
Antiparasite
|
ELQ-598 is a endochin-like quinolone compound with potent antibabesial activity with IC50 of 37 nM against B. duncani in human erythrocytes, the prodrug of ELQ-596. |
| PC-22513 |
ELQ-596
Antiparasite
|
ELQ-596 is a endochin-like quinolone compound with potent antibabesial activity with IC50 of 32 nM against B. duncani in human erythrocytes. |
| PC-22374 |
DDD00057570
Aminopeptidase M17 inhibitor
|
DDD00057570 is a selective inhibitor of Leishmania major M17 leucyl-aminopeptidase (LAP) with IC50 of 3.3 uM, exhibits in vitro antileishmanial activity. |
| PC-22373 |
MMV1557817
Aminopeptidase M1/M17 inhibitor
|
MMV1557817 is a selective, nanomolar inhibitor of both Plasmodium falciparum and Plasmodium vivax aminopeptidases M1 (Ki=308/19 nM) and M17 (Ki=112/208 nM), demonstrates potent activity against asexual and sexual stage parasites. |
| PC-22334 |
NPD8790
Complex I inhibitor
|
NPD8790 is a species-selective inhibitor of mitochondrial respiratory complex I with IC50 of 1.6, 2.1 and 1.1 uM for C. briggsae, P. pacificus and P. hermaphrodita complex I, respectively, does not inhibit human mitochondria with IC50 of >75 uM. |
| PC-21997 |
mCMY416
PheRS inhibitor
|
mCMY416 is a potent and selective inhibitor of Toxoplasma gondii phenylalanine tRNA synthetase (PheRS), potently inhibits T. gondii growth with EC90 of 0.38 uM. |
| PC-21960 |
NF2839
SmHDAC8 inhibitor
|
NF2839 is a quinolone-based HDAC inhibitor with IC50 of 0.1 uM for S. mansoni HDAC8 (SmHDAC8), inhibits S. mansoni larval stage with LD50 of 10.6 uM. |
| PC-21811 |
AWZ1066S
Wolbachia inhibitor
|
AWZ1066S is a potent, highly specific anti-Wolbachia inhibitor with EC50 of 2.5 nM against Wolbachia in cell-based assays, and IC50 of 121 nM in microfilaria assays. |
| PC-21802 |
MMV019266
Antibabesial inhibitor
|
MMV019266 is a potent antibabesial inhibitor with IC50 of 0.278 uM and 0.909 uM for Babesia spp. (B. bovis and B. divergens), respectively. |
| PC-21591 |
T. cruzi bc1 inhibitor compound 4
T. cruzi bc1 inhibitor
|
T. cruzi bc1 inhibitor compound 4 is a highly selective and efficacious T. cruzi cytochrome b inhibitor with IC50 of 6 nM, exhibits potent activity against intracellular amastigotes with EC50 of 0.08 uM. |
