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

Parasite

Parasite

Related Products

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

Parasite Isoform Specific Products:

Parasite Isoform Comparison
Cat. No. Product Name Effect Purity Chemical Structure
  • HY-101715
    Panidazole
    		Inhibitor 99.74%
    Panidazole is an amoebicide.
    Panidazole
  • HY-N7082R
    D-Arabinopyranose (Standard)
    		Inhibitor
    D-Arabinopyranose (Standard) is the analytical standard of D-Arabinopyranose. This product is intended for research and analytical applications. D-Arabinopyranose, a monosaccharide, shows strong growth inhibition against the Caenorhabditis elegans with an IC50 of 7.5 mM[1].
    D-Arabinopyranose (Standard)
  • HY-N0193R
    Artesunate (Standard)
    		Inhibitor 99.84%
    Artesunate (Standard) is the analytical standard of Artesunate. This product is intended for research and analytical applications. Artesunate is an inhibitor of both STAT-3 and exported protein 1 (EXP1).
    Artesunate (Standard)
  • HY-117897
    CK-2-68
    		Inhibitor 98.91%
    CK-2-68 is an inhibitor for complex III in protozoan mitochondrial respiratory chain, by targeting the alternative NADH dehydrogenase (NDH2) of the malarial parasite Plasmodium. CK-2-68 exhibits antimalaria efficacy, that inhibits Plasmodium falciparum infected erythrocytes with an IC50 of 40 nM.
    CK-2-68
  • HY-W588212
    trans-Permethrin
    		Inhibitor 99.88%
    trans-Permethrin is a transconfiguration of Permethrin (HY-B0887). Permethrin is an insecticide and neurotoxin.
    trans-Permethrin
  • HY-126425
    NCGC00262650
    		Inhibitor 99.22%
    NCGC00262650 is a potent apical membrane antigen 1-rhoptry neck protein 2 (AMA1-RON2) interaction inhibitor. NCGC00262650 can block entry of merozoites into red blood cells with an IC50 of 9.8 μM.
    NCGC00262650
  • HY-151217
    Ipronidazole
    		Inhibitor 99.10%
    Ipronidazole (RO-71554) is an orally active antihistomonal agent, which prevents and ameliorates enterohepatitis in turkeys. Ipronidazole can promotes turkey growth when supplied in feed or drinking water.
    Ipronidazole
  • HY-16973R
    Fluralaner (Standard)
    		Inhibitor
    Fluralaner (Standard) is the analytical standard of Fluralaner. This product is intended for research and analytical applications. Fluralaner (INN) is a systemic insecticide and acaricide Fluralaner through potent blockage of GABA and L-glutamate gated chloride channels.
    Fluralaner (Standard)
  • HY-N0337R
    Eugenol (Standard)
    		Inhibitor
    Eugenol (Standard) is the analytical standard of Eugenol. This product is intended for research and analytical applications. Eugenol is an essential oil found in cloves with antibacterial, anthelmintic and antioxidant activity. Eugenol is shown to inhibit lipid peroxidation.
    Eugenol (Standard)
  • HY-156895
    Ile-AMS
    		Inhibitor
    Ile-AMS is active active in P. falciparum, with an ABS IC50 of 1.19 nM.
    Ile-AMS
  • HY-164182S
    Myristoleyl carnitine-d3
    		Inhibitor 99.93%
    Myristoleyl carnitine-d3 is the deuterium labeled Myristoleyl carnitine(HY-164182).
    Myristoleyl carnitine-d<sub>3</sub>
  • HY-W342283
    Diminazene
    Diminazene is an aromatic diamidine compound primarily utilized for the control of trypanosomiasis, a disease caused by trypanosome parasites. Diminazene primarily binds to the kinetoplast DNA (kDNA) of the trypanosomes, interfering with their replication process. Diminazene also presents avenues for novel pharmacological applications, such as acting as an activator of angiotensin-converting enzyme 2 (ACE2), and showing potential in the treatment of hypertension, rheumatoid arthritis, and as an immunomodulator.
    Diminazene
  • HY-W009213
    3-Nitrophenyl disulfide
    		Inhibitor 99.23%
    3-Nitrophenyl disulfide (Bis(3-Nitrophenyl) disulfide) is an inhibitor of mannitol-1-phosphate dehydrogenase (M1PDH) with IC50 of 3 μM. 3-Nitrophenyl disulfide has antiparasitic activity.
    3-Nitrophenyl disulfide
  • HY-N7642
    Oxysanguinarine
    		Inhibitor 98.25%
    Oxysanguinarine (Hydroxysanguinarine;8-Oxosanguinarine) is a protoberberine alkaloid from Meconopsis simplicifolia with antimalarial activity.
    Oxysanguinarine
  • HY-130402A
    Propamidine isethionate
    Propamidine (isethionate) is an agent in the diamidine class. Propamidine (isethionate) can be used in research of Acanthamoeba keratitis.
    Propamidine isethionate
  • HY-B0223R
    Albendazole (Standard)
    		Inhibitor
    Albendazole (Standard) is the analytical standard of Albendazole. This product is intended for research and analytical applications. Albendazole (SKF-62979) is an orally active and broad-spectrum parasiticide with high effectiveness and low host toxicity, is used for the research of gastrointestinal parasites in humans and animals. Albendazole induces apoptosis and autophagy in cancer cells. Albendazole also inhibits tubulin polymerization and HIF-1α, VEGF expression, has antioxidant activity, and inhibits the glycolytic process in cancer cells.
    Albendazole (Standard)
  • HY-B1160
    Bitoscanate
    		Inhibitor ≥98.0%
    Bitoscanate (p-Phenylene diisothiocyanate) is an organic chemical compound used in the treatment of hookworms.
    Bitoscanate
  • HY-113752
    MMV019313
    		Inhibitor 99.54%
    MMV019313 is a potent, non-bisphosphonate inhibitor of farnesyl/geranylgeranyl diphosphate synthase (FPPS/GGPPS) with an IC50 of 0.82 µM. MMV019313 has activity against P. falciparum (Parasite).
    MMV019313
  • HY-119649S
    Flonicamid-15N18O
    		≥98.0%
    Flonicamid-15N,18O (IKI220-15N,18O) is 15N labeled Flonicamid. Flonicamid (IKI220) is a novel systemic insecticide with selective activity against hemipterous pests. The main insecticidal mechanism of flonicamid is starvation based on the inhibition of stylet penetration to plant tissues.
    Flonicamid-<sup>15</sup>N<sup>18</sup>O
  • HY-A0163D
    trans-Clopenthixol
    		Inhibitor 99.40%
    trans-Clopenthixol ((E)-Clopenthixol) is an antibiotic, without neuroleptic effect. trans-Clopenthixol can be used to inhibit Pseudomonas aeruginosa and Plasmodium falciparum in vitro.
    trans-Clopenthixol
Parasite Isoform Comparison

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