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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DC28424 | Dehydroemetine |
Dehydroemetine, a synthetic analogue of emetine dihydrochloride, is used for visceral leishmaniasis. Dehydroemetine used for anti-parasites.
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| DC8930 | Rafoxanide |
Rafoxanide is a salicylanilide used as an antiparasitic agent.
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| 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
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| DC7791 | NITD 609 |
NITD 609 is a novel and potent drug
candidate for the treatment of
uncomplicated malaria
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| 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
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| DC9360 | Buparvaquone |
Buparvaquone(Butalex) is a hydroxynaphthoquinone antiprotozoal drug related to parvaquone and atovaquone; it is a promising compound for the therapy and prophylaxis of all forms of theileriosis.
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| DC11738 | SCYX-7158 |
An orally-active, CNS permeable benzoxaborole antiprotozoal agent.
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| DC10303 | Allopurinol riboside |
Allopurinol riboside, a metabolite of allopurinol, shows potent activities against parasites.
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| DC11737 | GNF-6702 |
A selective, non-competitive inhibitor of the kinetoplastid proteasome, inhibits the chymotrypsin-like activity of the T. cruzi proteasome with IC50 of 35 nM.
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| DC11849 | DSM421 |
A potent, selective P. falciparum dihydroorotate dehydrogenase (PfDHODH) with IC50 of 53 nM.
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