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-153732
    Insecticidal agent 2
    		Inhibitor
    Insecticidal agent 2 (example 2) is a pesticide that exhibits potent growth-retarding activity against pests.
    Insecticidal agent 2
  • HY-N0059S6
    D-Arabinose-d6
    		Inhibitor
    D-Arabinose-d6 is the deuterium labeled D-Arabinose (HY-N0059). D-Arabinose is is an orally active antidepressant and a growth inhibitor of C. elegans (IC50 is 7.5 mM). D-Arabinose can penetrate the blood-brain barrier, selectively interfere with the metabolism of D-ribose and D-fructose, and inhibit the growth of nematodes. D-Arabinose can also inhibit the synthesis of cell biofilm and exert antibacterial activity. D-Arabinose activates the ACSS2-PPARγ/TFEB-CRTC1 axis through the lysosomal AXIN-LKB1-AMPK pathway, inducing CRTC1 transcription, exerts antidepressant-like activity. D-Arabinose is the ring-opened form of the aldopentose D-?Arabinose (HY-N7082).
    D-Arabinose-d<sub>6</sub>
  • HY-121817R
    Sulfiram (Standard)
    Sulfiram (Standard) is the analytical standard of Sulfiram (HY-121817). This product is intended for research and analytical applications. Sulfiram, an ectoparasiticide, is a weak aldehyde dehydrogenase (ALDH) inhibitor. Sulfiram can be used for the study of scabies.
    Sulfiram (Standard)
  • HY-108387
    Morantel citrate
    		Inhibitor
    Morantel citrate is a veterinary anthelmintic agent that inhibits parasitic infections in cattle, sheep and goats. Morantel citrate paralyzes the nervous system of the parasite, helping the animal expel the dead parasite from the body.
    Morantel citrate
  • HY-117419
    (-)-Lavandulyl acetate
    		Inhibitor
    (-)-Lavandulyl acetate is a nature product that can be found in Lavandula angustifolia. (-)-Lavandulyl acetate shows toxicity for mosquito vectors. (-)-Lavandulyl acetate can be used as mosquito larvicide.
    (-)-Lavandulyl acetate
  • HY-147535
    Antileishmanial agent-7
    		Inhibitor
    Antileishmanial agent-7 (compound 23) is a potent antileishmanial agent. Antileishmanial agent-7 shows antileishmanial activity against Leishmania donovani and L-6, with IC50 values of 6.89 and 259 μM, respectively.
    Antileishmanial agent-7
  • HY-143322
    CRK12-IN-2
    		Inhibitor
    CRK12-IN-2 (compound 2) is an inhibitor of CRK12. CRK12-IN-2 shows potency against Trypanosoma congolense and Trypanosoma vivax with EC50 values of 3.2 and 0.08 nM. CRK12-IN-2 can be used for the research of animal trypanosomiasis.
    CRK12-IN-2
  • HY-123686
    Ivermectin B1a monosaccharide
    		Inhibitor
    Ivermectin B1a monosaccharide is a modified Ivermectin B1a (HY-126937). Ivermectin B1a monosaccharide is an antiparasite agent with a minimum concentration for full activity in Haemonchus contortus larval development of 0.001 μg/mL.
    Ivermectin B1a monosaccharide
  • HY-119893
    Diamfenetide
    		Inhibitor 99.72%
    Diamfenetide is used for the study of Fasciola hepatica infections in vitro. Diamfenetide leads to irreversible paralysis in vitro of immature and adult Fasciola hepatica.
    Diamfenetide
  • HY-N8338
    Pancixanthone A
    		Inhibitor
    Pancixanthone A is a xanthone that can be isolated from Garcinia vieillardii. Pancixanthone A has antimalarial activity against chloroquino-resistant strains of Plasmodium falciparum with an IC50 of 1.6 μg/mL.
    Pancixanthone A
  • HY-132908
    Anti-ToCV agent 1
    		Inhibitor
    Anti-ToCV agent 1 can be used as a potential anti-ToCV agent.
    Anti-ToCV agent 1
  • HY-N2970
    Burchellin
    		Inhibitor
    Burchellin is a neolignan that can inhibit Trypanosoma cruzi.
    Burchellin
  • HY-N0769R
    Isopimpinellin (Standard)
    		Inhibitor
    Isopimpinellin (Standard) is the analytical standard of Isopimpinellin. This product is intended for research and analytical applications. Isopimpinellin, an orally active compound isolated from Glomerella cingulata. Isopimpinellin blocks DNA adduct formation and skin tumor initiation by 7,12-dimethylbenz[a]anthracene. Isopimpinellin possesses anti-leishmania effect.
    Isopimpinellin (Standard)
  • HY-147534
    Antileishmanial agent-6
    		Inhibitor
    Antileishmanial agent-6 (compound 8m) is a potent antileishmanial agent. Antileishmanial agent-6 shows antileishmanial and cytotoxic activity against Leishmania donovani and L-6, with IC50 values of 0.54 and 10.2 μM, respectively.
    Antileishmanial agent-6
  • HY-123897
    Chamaejasmenin C
    		Inhibitor
    Chamaejasmenin C, a biflavanone, shows nematicidal activity against second-stage juveniles (J2s) of B. xylophilus and B. mucronatus.
    Chamaejasmenin C
  • HY-126869
    Pseudomonic acid D
    		Inhibitor
    Pseudomonic acid D is a microbial inhibitor. Pseudomonic acid D potently inhibits mycoplasmas and bacterial pathogens. Pseudomonic acid D can be produced by fermentation with Pseudomonas fluorescens.
    Pseudomonic acid D
  • HY-B1322AS1
    Amodiaquine-d10 hydrochloride
    		Inhibitor
    Amodiaquine-d10 hydrochloride is deuterated labeled Amodiaquine (HY-B1322A). Amodiaquine (Amodiaquin), a 4-aminoquinoline class of antimalarial agent, is a potent and orally active histamine N-methyltransferase inhibitor. Amodiaquine is also a Nurr1 agonist and specifically binds to Nurr1-LBD (ligand binding domain) with an EC50 of ~20 μM. Anti-inflammatory effect.
    Amodiaquine-d<sub>10</sub> hydrochloride
  • HY-W011239
    Fenbendazole sulfone
    		Inhibitor
    Fenbendazole sulfone (Oxfendazole sulfone;FBZ-SO2) is a minor metabolite of Fenbendazole in plasma and is a benzimidazole anthelmintic agent.
    Fenbendazole sulfone
  • HY-157840
    Anti-infective agent 9
    		Inhibitor
    Anti-infective agent 9 (compound 1) is a Plasmodium falciparum inhibitor (IC50=600 nM), can downregulate pyruvate levels and TCA cycle in Plasmodium. Anti-infective agent 9It has good metabolic stability and low toxicity to human liver cells. The study found, Anti-infective agent 9Potential targets for inhibiting Plasmodium falciparum are not 1-deoxidation-d-xylulose-5-Phosphate synthase (DXPS).
    Anti-infective agent 9
  • HY-122382
    Levofuraltadone
    		Inhibitor
    Levofuraltadone (NF-602) is an antibacterial and antiparasitic agent. Levofuraltadone has anti-trypanosomiasis activity and can be used in the study of human african trypanosomiasis as well as bacterial infections.
    Levofuraltadone
Parasite Isoform Comparison

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