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-B0565S
    Ronidazole-d3
    		Inhibitor
    Ronidazole-d3 is the deuterium labeled Ronidazole (HY-B0565). Ronidazole is a potent and orally active antiprotozoal and anti-microbial agent. Ronidazole acts as a veterinary agent against Tritrichomonas foetus?in cats models. Ronidazole can be used the research of forhistomoniasis?and?swine?dysentery.
    Ronidazole-d<sub>3</sub>
  • HY-145704
    Antimalarial agent 8
    		Inhibitor
    Antimalarial agent 8 (Compound 7e) is a novel orally active class of antimalarials. Antimalarial agent 8 is potent in vitro against P. falciparum and is orally efficacious (40 mg/kg) in an in vivo mouse model of malaria.
    Antimalarial agent 8
  • HY-115584S
    Lufenuron-13C6
    		Inhibitor
    Lufenuron-13C6 is a 13C-labeled Lufenuron. Lufenuron is a lipophilic benzoylurea insecticide and a chitin synthesis inhibitor that can used for flea and fish lice control. Lufenuron inhibits moulting of arthropods[1][2].
    Lufenuron-<sup>13</sup>C<sub>6</sub>
  • HY-B1851R
    Hexythiazox (Standard)
    		Inhibitor
    Hexythiazox (Standard) is the analytical standard of Hexythiazox. This product is intended for research and analytical applications. Hexythiazox is a selective acaricide with ovicidal, larvicidal and nymphicidal activities. Hexythiazox is widely used for chemical control of mites on cotton, fruits and vegetables. Hexythiazox is harmless to mammals and has no effect on beneficial insects and predators of mites.
    Hexythiazox (Standard)
  • HY-B1073R
    Morantel tartrate (Standard)
    		Inhibitor
    Morantel (tartrate) (Standard) is the analytical standard of Morantel (tartrate). This product is intended for research and analytical applications.
    Morantel tartrate (Standard)
  • HY-155693
    Topoisomerase II inhibitor 16
    		Inhibitor
    Topoisomerase II inhibitor 16 (compound CT3) is a selective, orally active, brain-penetrant and irreversible trypanosomal topoisomerase II inhibitor by stabilizing double-stranded DNA:enzyme cleavage complexes. Topoisomerase II inhibitor 16 has the potential for Chagas disease research.
    Topoisomerase II inhibitor 16
  • HY-Q40175
    Antitrypanosomal agent 9
    		Inhibitor
    Antitrypanosomal agent 9 (compound 1) is a potent antitrypanosomal agent. Antitrypanosomal agent 9 shows inhibitory activity against T. b. brucei, with an IC50 of 1.15 μM. Antitrypanosomal agent 9 can be used for human African trypanosomiasis (HAT) research.
    Antitrypanosomal agent 9
  • HY-125729
    Ivermectin B1b
    		Inhibitor 98.66%
    Ivermectin B1b is the minor component of Ivermectin. Ivermectin, a potent anti-parasitic agent, inhibits the replication of SARS-CoV-2 in cell culture.
    Ivermectin B1b
  • HY-116713
    PfDHODH-IN-3
    PfDHODH-IN-3 (compound 2) is an orally active PfDHODH inhibitor with strong antimalarial activity (IC50=47 nM). PfDHODH-IN-3 can inhibit the growth of Plasmodium in animals.
    PfDHODH-IN-3
  • HY-17506R
    Azithromycin (Standard)
    Azithromycin (Standard) is the analytical standard of Azithromycin. This product is intended for research and analytical applications. Azithromycin is a macrolide antibiotic useful for the treatment of a number of bacterial infections.
    Azithromycin (Standard)
  • HY-B2186R
    Piperazine adipate (Standard)
    		Inhibitor
    Piperazine adipate (Standard) is the analytical standard of Piperazine adipate. This product is intended for research and analytical applications. Piperazine adipate is a potent broad spectrum anthelmintic against many common worm infections in mammals.
    Piperazine adipate (Standard)
  • HY-17596S
    Closantel-13C6
    		Inhibitor
    Closantel-13C6 is the 13C6 labeled Closantel. Closantel is a halogenated salicylanilide with a potent anti-parasitic activity. Closantel is a potent and highly specific Onchocerca volvulus chitinase (OvCHT1) inhibitor with an IC50 of 1.6 μM and a Ki of 468 nM. Closantel inhibits the O. volvulus L3 to L4 molt of developing.
    Closantel-<sup>13</sup>C<sub>6</sub>
  • HY-B0826R
    Spirodiclofen (Standard)
    		Inhibitor
    Spirodiclofen (Standard) is the analytical standard of Spirodiclofen. This product is intended for research and analytical applications.
    Spirodiclofen (Standard)
  • HY-B1953S
    Thiacloprid-d4
    Thiacloprid-d4 is the deuterium labeled Thiacloprid[1]. Thiacloprid, a chloronicotinyl insecticide, is targeted chiefly to control aphid pest species in orchards and vegetables[1]. Thiacloprid destabilizes DNA. Thiacloprid changes the structure and stability of DNA through binding into the minor groove by hydrophobic or hydrogen interactions[2].
    Thiacloprid-d<sub>4</sub>
  • HY-108640
    HLI373
    		Inhibitor
    HLI373 is an efficacious Hdm2 inhibitor. HLI373 inhibits the ubiquitin ligase activity of Hdm2. HLI373 is effective in inducing apoptosis of several tumor cells that are sensitive to DNA-damaging agents. Antimalarial activity.
    HLI373
  • HY-149937
    Antimalarial agent 24
    		Inhibitor
    Antimalarial agent 24 (Compound 7) is an antimalarial agent in vitro. Antimalarial agent 24 inhibits P. falciparum W2 strain with an IC50 of 0.81 μM. Antimalarial agent 24 displays a CC50 higher than 200 μM against HepG2 cells.
    Antimalarial agent 24
  • HY-B1315S
    Carbaryl-d3
    Carbaryl-d3 is the deuterium labeled N6-(carboxymethyl)-L-lysine[1].
    Carbaryl-d<sub>3</sub>
  • HY-P4757
    N1-Glutathionyl-spermidine disulfide
    		Inhibitor
    N1-Glutathionyl-spermidine disulfide is a substrate of trypanothione reductase.
    N1-Glutathionyl-spermidine disulfide
  • HY-B1751A
    Quinidine sulfate
    		Inhibitor
    Quinidine Monosulfate is an antiarrhythmic agent. Quinidine Monosulfate is a potent, orally active, selective cytochrome P450db inhibitor. Quinidine Monosulfate is also a K+ channel blocker with an IC50 of 19.9 μM, and can induce apoptosis. Quinidine Monosulfate can be used for malaria research.
    Quinidine sulfate
  • HY-125159
    Derquantel
    		Inhibitor
    Derquantel is a potent anthelmintic. Derquantel causes flaccid paralysis and expulsion of nematodes.
    Derquantel
Parasite Isoform Comparison

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