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-119714
    Ambelline
    Inhibitor
    Ambelline is an alkaloid that can be isolated from the Amaryllidaceae family. Ambelline shows antimalarial activity against Dd2 P. falciparum strain, with an IC50 of 7.3 ± 0.3 μM.
    Ambelline
  • HY-W079315
    5-Phenylthieno[2,3-d]pyrimidin-4-amine
    5-Phenylthieno[2,3-d]pyrimidin-4-amine (Compound 3b) is a heterocyclic compound with antiviral and antiprotozoal activities.
    5-Phenylthieno[2,3-d]pyrimidin-4-amine
  • HY-155401
    Antitrypanosomal agent 18
    Inhibitor
    Antitrypanosomal agent 18 (compound 8b) is a nitrofuran derivative has strong trypanocidal activity in vitro with an IC50 value of 0.03 μM.
    Antitrypanosomal agent 18
  • HY-N12232
    Carbazomycin D
    Inhibitor
    Carbazomycin D exhibits antituberculosis and antimalarial activities, that inhibits Plasmodium falciparum with an IC50 > 10 μg/mL, inhibits Mycobacterium tuberculosis with MIC of 25 μg/mL. Carbazomycin D exhibits cytotoxicity in cell MCF-7, KB, NCI-H187 and Vero, with IC50s of 21.3, 33.2, 12.9, and 34.3 μg/mL, respectively.
    Carbazomycin D
  • HY-W780803
    (Z,E)-9,12-Tetradecadienol
    Inhibitor
    (Z,E)-9,12-Tetradecadienol is a synthetic enhancer of male Ephestia cautella attraction.
    (Z,E)-9,12-Tetradecadienol
  • HY-163780
    AChE-IN-66
    Inhibitor
    Nematicidal agent 1 is a potent nematicidal agent. Nematicidal agent 1 binds to the pocket of acetylcholine esterase (AChE).
    AChE-IN-66
  • HY-13832R
    Atovaquone (Standard)
    Inhibitor
    Atovaquone (Standard) is the analytical standard of Atovaquone. This product is intended for research and analytical applications. Atovaquone (Atavaquone) is a potent, selective and orally active inhibitor of the parasite’s mitochondrial cytochrome bc1 complex. Atovaquone is against human and  P. falciparum cytochrome bc1 activity with IC50 values of 460 nM and 2.0 nM, respectively. Atovaquone is an antimalarial agent and has the potential for the investigation of neumocystis pneumonia, toxoplasmosis, malaria, and babesia.
    Atovaquone (Standard)
  • HY-N8484
    Eprinomectin B1b
    Eprinomectin B1b is a minor component and belongs to the avermectin family of insecticides and anthelmintics.
    Eprinomectin B1b
  • HY-W018025R
    5,6-Dihydroxyindole (Standard)
    Inhibitor
    5,6-Dihydroxyindole (Standard) is the analytical standard of 5,6-Dihydroxyindole. This product is intended for research and analytical applications. 5,6-Dihydroxyindole, a melanin precursor, has a broad-spectrum antibacterial, antifungal, antiviral, antiparasitic activity. 5,6-Dihydroxyindole has cytotoxic effects and is strongly toxic against various pathogens.
    5,6-Dihydroxyindole (Standard)
  • HY-N13288
    Cordysinin C/D
    Inhibitor
    Cordysinin C/D (compound 9) is a potential anti-plasmodial compound that can effectively inhibit Plasmodium falciparum 3D7 strain.
    Cordysinin C/D
  • HY-N15187
    Acronycidine
    Inhibitor
    Acronycidine is a quinoline alkaloid with antimalarial activity and can be extracted from Acronychia baueri Schott. Acronycidine can be utilized in malari research.
    Acronycidine
  • HY-B1953R
    Thiacloprid (Standard)
    Inhibitor
    Thiacloprid (Standard) is the analytical standard of Thiacloprid. This product is intended for research and analytical applications. Thiacloprid, a chloronicotinyl insecticide, is targeted chiefly to control aphid pest species in orchards and vegetables. Thiacloprid destabilizes DNA. Thiacloprid changes the structure and stability of DNA through binding into the minor groove by hydrophobic or hydrogen interactions.
    Thiacloprid (Standard)
  • HY-W357413
    Chinifur
    Inhibitor
    Chinifur (Quinifuryl), a Nitrofuran derivative, is a selective inhibitor of trypanothione reductase and also a radical-generating substrate for trypanothione reductase (Ki = 4.5 μM).
    Chinifur
  • HY-168069
    DHFR-IN-20
    Inhibitor
    DHFR-IN-20 (Compound LA1) is a Plasmodium falciparum dihydrofolate reductase (DHFR) inhibitor, with Kis of 0.16, 0.30, 6.6 nM for PfDHFR-WT, PfDHFR-QM, HsDHFR. DHFR-IN-20 has antimalarial activities (IC50: 1.4 nM and 1.6 μM for P. falciparum carrying the wild-type (TM4/8.2) and the quadruple mutant (V1/S) PfDHFR enzyme.
    DHFR-IN-20
  • HY-N14068
    Cytosaminomycin B
    Inhibitor
    Cytosaminomycin B has anti-Eimeria Tenella activity.
    Cytosaminomycin B
  • HY-N8374
    Pheanthine
    Inhibitor
    Pheanthine (Compound 2) is an antiplasmodial agent, that inhibits chloroquine-resistant Plasmodium falciparum K-1 (IC50 is 0.8 μM) and chloroquine-sensitive P. falciparum strain NF54 A19A (IC50 of 0.03 μM). Pheanthine exhibits low cytotoxicity in human lung fibrosblast (MRC-5, IC50 is 11.2 μM) and macrophages (PMM, IC50 is 8 μM).
    Pheanthine
  • HY-B0840R
    Chlorfenapyr (Standard)
    Chlorfenapyr (Standard) is the analytical standard of Chlorfenapyr. This product is intended for research and analytical applications. Chlorfenapyr is a pyrrole insecticide. Chlorfenapyr has a mode of action: the mixed function oxidase oxidizes and removes the Nethoxymethyl group to form the active metabolite, CL 303268. Chlorfenapyr is used for termite control and crop protection against a variety of insect and mite pests.
    Chlorfenapyr (Standard)
  • HY-N14069
    Cytosaminomycin C
    Inhibitor
    Cytosaminomycin C has anti-Eimeria Tenella activity.
    Cytosaminomycin C
  • HY-B0433AR
    Quinine (hydrochloride dihydrate) (Standard)
    Inhibitor
    Quinine (hydrochloride dihydrate) (Standard) is the analytical standard of Quinine (hydrochloride dihydrate). This product is intended for research and analytical applications. Quinine hydrochloride dihydrate (Qualaquin) is an orally active and can be used in anti-malarial studies. Quinine hydrochloride dihydrate is a potassium channel inhibitor that inhibits WT mouse Slo3 (KCa5.1) channel currents evoked by voltage pulses to +100?mV with an IC50 of 169 μM.
    Quinine (hydrochloride dihydrate) (Standard)
  • HY-N0565AS
    Doxycycline-d3 hydrochloride
    Doxycycline-d3 hydrochloride is deuterium labeled Doxycycline (hydrochloride). Doxycycline hydrochloride, an antibiotic, is an orally active and broad-spectrum metalloproteinase (MMP) inhibitor. Doxycycline hydrochloride shows antibacterial activity and anti-cancer cell proliferation activity.
    Doxycycline-d<sub>3</sub> hydrochloride

Your Search Returned No Results.

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

Please try each isoform separately.