| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DC11849 | DSM421 | A potent, selective P. falciparum dihydroorotate dehydrogenase (PfDHODH) with IC50 of 53 nM. |
|
| DC11738 | SCYX-7158 | An orally-active, CNS permeable benzoxaborole antiprotozoal agent. |
|
| DC11409 | DSM265 Featured | DSM265 is a PfDHODH inhibitor with an IC50 of 8.9 nM. DSM265 can also inhibit the growth of P. falciparum 3D7 parasites with an EC50 of 4.3 nM. |
|
| DC10301 | Emodepside Featured | Emodepside (PF 1022-221) is a cyclooctadepsipeptide with broad-spectrum anthelmintic activity. |
|
| DC10258 | Mebendazole | Mebendazole is a synthetic benzimidazole derivate and anthelmintic agent. Mebendazole interferes with the reproduction and survival of helminths by inhibiting the formation of their cytoplasmic microtubules, thereby selectively and irreversibly blocking g |
|
| DC7791 | NITD 609 | NITD 609 is a novel and potent drug candidate for the treatment of uncomplicated malaria |
|
| DCAPI1553 | Pyrimethamine | Pyrimethamine is a potent inhibitor of multi-drug and toxin extrusion transporters. This compound inhibits Mdr-1(Pgp) and thus allows for active drugs to stay within the cell for longer periods of time, increasing their effectiveness by preventing efflux |
|
| DC8930 | Rafoxanide | Rafoxanide is a salicylanilide used as an antiparasitic agent. |
|
| DC8336 | Tizoxanide Featured | Tizoxanide is a potent inhibitor of hepatitis B virus and hepatitis C virus. |
|
