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.

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-163776
    Insecticidal agent 13
    Inhibitor
    Insecticidal agent 13 (compound A15) is a phenylpyrazole derivative with insecticidal and acaricidal activities, which can be used in the research of agricultural pest control.
    Insecticidal agent 13
  • HY-B0291R
    Oxfendazole (Standard)
    Inhibitor
    Oxfendazole (Standard) is the analytical standard of Oxfendazole. This product is intended for research and analytical applications. Oxfendazole is the sulfoxide form of fenbendazole, which fights parasites.
    Oxfendazole (Standard)
  • HY-14749AR
    Pyronaridine tetraphosphate (Standard)
    Inhibitor
    Pyronaridine (tetraphosphate) (Standard) is the analytical standard of Pyronaridine (tetraphosphate). This product is intended for research and analytical applications. Pyronaridine tetraphosphate is an orally active Mannich base anti-malarial agent. Pyronaridine tetraphosphate is active against P. falciparum and Echinococcus granulosus infection.
    Pyronaridine tetraphosphate (Standard)
  • HY-17532R
    Haloxon (Standard)
    Inhibitor
    Haloxon (Standard) is the analytical standard of Haloxon. This product is intended for research and analytical applications. Haloxon is an anti-parasitic agent. Haloxon can be used for the research of infections of Parascaris equorum, Oxyuris equi and Strongylus vulgaris. Haloxon also can be used in control of ascarids and hookworms in domesticated animals in combination with Bidimazium.
    Haloxon (Standard)
  • HY-175517
    PEX5-PEX14 PPI-IN-3
    Inhibitor
    PEX5-PEX14 PPI-IN-3 (Compound 7) is an inhibitor of the PEX5-PEX14 protein-protein interaction (PPI) with an EC50 of 95 μM. PEX5-PEX14 PPI-IN-3 has an EC50 of 7.2 μM against Trypanosoma brucei (T. brucei). PEX5-PEX14 PPI-IN-3 exhibits low cytotoxicity towards HepG2 cells and possesses antiparasitic activity.
    PEX5-PEX14 PPI-IN-3
  • HY-118412
    Terallethrin
    Inhibitor
    Terallethrin (M108) is a synthetic pyrethroid widely used as an insecticide in agricultural and household Settings.
    Terallethrin
  • HY-N2876
    Anisofolin A
    Inhibitor
    Anisofolin A is a flavonoid that can be isolated from Anisomeles indica. Anisofolin A has antimalarial activity (IC50: 4.39 μM), and antimycobacterium activity (IC50: 4.50 μM) against M. tuberculosis H37Ra.
    Anisofolin A
  • HY-136783
    G6PD-IN-2
    Inhibitor
    G6PD-IN-2 is a Plasmodium falciparum glucose-6-phosphate dehydrogenase (G6PD) inhibitor with an IC50 value of 0.2 μM. G6PD-IN-2 exerts weak inhibitory activity on Plasmodium falciparum glucose-6-phosphate dehydrogenase-6-phosphogluconolactonase (PfGluPho) with an IC50 value of 22.0 μM. G6PD-IN-2 inhibits growth of Plasmodium falciparum 3D7 strain and exhibits low cytotoxicity in hepatocytes. G6PD-IN-2 can be used for the research of malaria.
    G6PD-IN-2
  • HY-N1667R
    2',4'-Dihydroxy-6'-Methoxyacetophenone (Standard)
    Inhibitor
    2',4'-Dihydroxy-6'-Methoxyacetophenone is a phenolic acetophenone from Artemisia annua. Artemisia annua is an analog of Artemisinin that is effective in the research of malaria.
    2',4'-Dihydroxy-6'-Methoxyacetophenone (Standard)
  • HY-177441
    Apicidin C
    Inhibitor
    Apicidin C (Compound 5a) is a cyclic tetrapeptide. Apicidin C has an antiprotozoal and antimalarial activity against Eimeria tenella (IC50: 6 nM) by reversibly inhibiting HDAC acyivity. Apicidin C can be used for malaria infections research.
    Apicidin C
  • HY-B0529R
    Azlocillin (Standard)
    Inhibitor
    Azlocillin (Standard) is the analytical standard of Azlocillin. This product is intended for research and analytical applications. Azlocillin, an antibiotic, is a semisynthetic penicillin, and has broad-spectrum antibacterial activity. Azlocillin is active against drug-tolerant B. burgdorferi sensu stricto JLB31 infection.
    Azlocillin (Standard)
  • HY-182621
    MB4253
    Inhibitor
    MB4253 is an orally active aliphatic amide and schistosomicidal agent. MB4253 acts against Schistosoma mansoni. MB4253 can be used for the research of schistosomiasis.
    MB4253
  • HY-A0106R
    Levamisole (Standard)
    Inhibitor
    Levamisole (Standard) is the analytical standard of Levamisole. This product is intended for research and analytical applications. Levamisole ((-)-Levamisole), an anthelmintic agent with immunomodulatory properties. Levamisole acts as a positive allosteric modulator (PAM) for the α3β2 (EC50=300 μM) and α3β4 (EC50=100 μM) subtype of nAChRs. Orally active.
    Levamisole (Standard)
  • HY-B2029R
    Phosalone (Standard)
    Inhibitor
    Phosalone (Standard) is the analytical standard of Phosalone. This product is intended for research and analytical applications.
    Phosalone (Standard)
  • HY-171190
    ELQ-316
    Inhibitor
    ELQ-316 is an endochinlike quinolone compound and an anti-parasite agent. ELQ-316 demonstrates a great efficacy against acute and chronic experimental toxoplasmosis.
    ELQ-316
  • HY-126392
    Isonardoperoxide
    Inhibitor
    Isonardoperoxide is a potent antimalaria agent with an EC50 of 0.6 μM for Plasnwdium fulciparum malaria.
    Isonardoperoxide
  • HY-130752
    VNI
    Inhibitor
    VNI is an effective inhibitor of CYP51. VNI can inhibit sterol synthesis in Trypanosoma cruzi, exhibiting anti-Trypanosoma cruzi activity.
    VNI
  • HY-B1344R
    Oxantel pamoate (Standard)
    Inhibitor
    Oxantel pamoate (Standard) (Oxantel embonate (Standard)) is the analytical standard of Oxantel pamoate (HY-B1344). This product is intended for research and analytical applications. Oxantel pamoate (Oxantel embonate) is an anthelmintic agent that potently against Trichuris muris. Oxantel pamoate inhibits fumarate reductase (Frd) activity in some pathogenic bacteria and inhibits P. gingivalis homotypic biofilm formation (IC50 of 2.2 μM).
    Oxantel pamoate (Standard)
  • HY-134220
    Doramectin monosaccharide
    Doramectin monosaccharide is an acid degradation product of Doramectin (HY-17035), a disaccharide-containing anthelmintic that potentiates glutamate- and GABA-gated chloride channel opening in nematodes. Doramectin undergoes acid-catalyzed hydrolysis to form doramectin monosaccharide.
    Doramectin monosaccharide
  • HY-180158
    Antitrypanosomal agent 28
    Inhibitor
    Antitrypanosomal agent 28 (Compound 2a) is a trypanocidal agent. Antitrypanosomal agent 28 effectively inhibits Trypanosoma cruzi by inducing the generation of ROS and mitochondrial damage, with an IC₅₀ of 49.4 μM. Antitrypanosomal agent 28 exhibits broad-spectrum anti-tumor activity against various tumor cell lines, especially being sensitive to leukemia, colon cancer, and breast cancer. Antitrypanosomal agent 28 can be used for research on anti-cancer and anti-trypanosome activities.
    Antitrypanosomal agent 28

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