1. Signaling Pathways
  2. Anti-infection
  3. Parasite

Parasite

Antiparasitics are a class of medications which are indicated for the treatment of parasitic diseases such as nematodes, cestodes, trematodes, and infectious protozoa.

Parasite Related Products (192):

Cat. No. Product Name Effect Purity
  • HY-B1370
    Hydroxychloroquine sulfate Inhibitor 99.99%
    Hydroxychloroquine sulfate is a synthetic antimalarial drug which can also inhibit Toll-like receptor 7/9 (TLR7/9) signaling.
  • HY-B1479B
    Emetine dihydrochloride hydrate Inhibitor 99.81%
    Emetine dihydrochloride hydrate is an anti-protozoal drug previously used for intestinal and tissue amoebiasis.
  • HY-B0318
    Metronidazole Inhibitor
    Metronidazole is a nitroimidazole antibiotic medication used particularly for anaerobic bacteria and protozoa.
  • HY-N0176
    Dihydroartemisinin Inhibitor 99.03%
    Dihydroartemisinin is a potent anti-malaria agent.
  • HY-16973
    Fluralaner Inhibitor 99.87%
    Fluralaner (INN) is a systemic insecticide and acaricide Fluralaner through potent blockage of GABA and L-glutamate gated chloride channels.
  • HY-B1479A
    Emetine dihydrochloride Inhibitor >99.0%
    Emetine (dihydrochloride) is an anti-protozoal drug previously used for intestinal and tissue amoebiasis.
  • HY-13836
    ELQ-300 Inhibitor 98.59%
    ELQ-300 is a potent and orally bioavailable antimalarial agent, acts as an inhibitor of the reductive (Qi) site of the cytochrome bc1 complex (cyt bc1).
  • HY-16762
    Artefenomel 99.41%
    Artefenomel (OZ439) is a synthetic antimalarial agent with the artemisinin pharmacophore. Artefenomel (OZ439) is a long-acting artemisinin-related agent.
  • HY-15310
    Ivermectin Activator >98.0%
    Ivermectin (MK-933) is a broad-spectrum anti-parasite medication used in humans most commonly to treat nematode infections such as onchocerciasis, as well as scabies and lice. Ivermectin (MK-933) is a specific inhibitor of Impα/β1-mediated nuclear import and has potent antiviral activity towards both HIV-1 and dengue virus. It is a positive allosteric effector of P2X4 and the α7 neuronal nicotinic acetylcholine receptor (nAChRs).
  • HY-B0094
    Artemisinin Inhibitor >98.0%
    Artemisinin (Qinghaosu), a sesquiterpene lactone, is an anti-malarial drug isolated from the aerial parts of Artemisia annua L. plants. Artemisinin inhibits AKT signaling pathway by decreasing pAKT in a dose-dependent manner. Artemisinin reduces cancer cell proliferation, migration, invasion, tumorigenesis and metastasis and has neuroprotective effects.
  • HY-16438
    RRx-001 Inhibitor 99.82%
    RRx-001, a hypoxia-selective epigenetic agent and studied as a radio- and chem-sensitizer, triggers apoptosis and overcomes drug resistance in myeloma. RRx-001 exhibits potent anti-tumor activity with minimal toxicity. RRx-001 is a dual small molecule checkpoint inhibitor by downregulating CD47 and SIRP-α. RRx-001 is a potent inhibitor of G6PD and shows potent antimalarial activity.
  • HY-13666
    Levamisole hydrochloride Inhibitor 99.96%
    Levamisole hydrochloride is an anthelmintic and immunomodulator belonging to a class of synthetic imidazothiazole derivatives.
  • HY-17592
    Bithionol Inhibitor >99.0%
    Bithionol is a clinically approved anti-parasitic drug; has been shown to inhibit solid tumor growth in several preclinical cancer models.
  • HY-17595
    Mebendazole Inhibitor 99.88%
    Mebendazole is a highly effective, broad-spectrum antihelmintic indicated for the treatment of nematode infestations; has been found as a hedgehog inhibitor.
  • HY-B1751
    Quinidine Inhibitor >98.0%
    Quinidine is an antiarrhythmic agent for the treatment of abnormal heart rhythms and also malaria.
  • HY-15311
    Avermectin B1 Inhibitor
    Avermectin B1 (Abamectin) is a widely used insecticide and anthelmintic.
  • HY-17596
    Closantel Inhibitor >98.0%
    Closantel is a salicylanilide anthelmintic compound; exhibits different anthelmintic spectra and apparent toxicity in mammals.
  • HY-14989
    SQ109 Inhibitor >98.0%
    SQ109 is a potent inhibitor of the trypomastigote form of the parasite, with IC50 for cell killing of 50±8 nM. SQ109, targets MmpL3, is an antitubercular agent.
  • HY-14430
    Cipargamin Inhibitor >98.0%
    Cipargamin (NITD609) is an potent antimalarial compound, with IC50 of appr 1 nM against P. falciparum.
  • HY-100184
    DSM265 Inhibitor 99.59%
    DSM265 is a long-duration inhibitor of P. falciparum dihydroorotate dehydrogenase (PfDHODH) with an IC50 of 8.9 nM. DSM265 can also inhibit the growth of Pf3D7 parasites with an EC50 of 4.3 nM.
Isoform Specific Products

Your Search Returned No Results.

Sorry. There is currently no product that acts on isoform together.

Please try each isoform separately.