Parasite

Parasite

Parasite

Related Products

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

Parasite Related Products (1991)
Related Compound Screening Libraries (1)
Parasite Isoform Comparison

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By Effects:	Controls (10) Inhibitors (1660) Agonist (1) Antagonist (1) Activators (2) Modulators (3)

Cat. No.	Product Name	Effect	Purity	Chemical Structure

HY-W743562

Crotamiton-d₅	Inhibitor
Crotamiton-d₅ is deuterium-labeled Crotamiton (HY-B1177).

HY-118412

Terallethrin	Inhibitor
Terallethrin (M108) is a synthetic pyrethroid widely used as an insecticide in agricultural and household Settings.

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.

HY-N12700

Puberulic acid Ⅰ	Inhibitor
Puberulic acid Ⅰ possesses anti-malarial activity with an IC₅₀ value of 0.050 µM against Plasmodium falciparum K1 (chloroquine-resistant).

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.

HY-W015818R

2-Benzoxazolinone (Standard)	Inhibitor
2-Benzoxazolinone (Standard) is the analytical standard of 2-Benzoxazolinone. This product is intended for research and analytical applications. 2-Benzoxazolinone is an anti-leishmanial agent with an LC50 of 40 μg/mL against L. donovani. A building block in chemical synthesis. 1,3-Benzoxazol-2(3H)-one derivatives have antimicrobial activity against a selection of Gram-positive, Gram-negative bacteria and yeasts. Derivatives as anti-quorum sensing agent[4].

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.

HY-B2029R

Phosalone (Standard)	Inhibitor
Phosalone (Standard) is the analytical standard of Phosalone. This product is intended for research and analytical applications.

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.

HY-169790

Phomarin	Inhibitor
Phomarin is an inhibitor for dihydrofolate reductase (DHFR), and exhibits potential antimalarial activity.

HY-126392

Isonardoperoxide	Inhibitor
Isonardoperoxide is a potent antimalaria agent with an EC₅₀ of 0.6 μM for Plasnwdium fulciparum malaria.

HY-137034

(+)-Secolongifolene-diol
(+)-Secolongifolene-diol is a sesquiterpene, that can be isolated from the marine fungal Drechslera sp. (+)-Secolongifolene-diol exhibits slightly weak effectiveness in antioxidation, antimicrobial and antifouling aspects.

HY-130752

VNI	Inhibitor
VNI is an effective inhibitor of CYP51. VNI can inhibit sterol synthesis in Trypanosoma cruzi, exhibiting anti-Trypanosoma cruzi activity.

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).

HY-169339

Villalstonine	Inhibitor
Villalstonine is a bisindole alkaloid with various biological activities including anticancer, antimalarial, and antiamoebic activities. Villalstonine exhibits potent antiplasmodial activity against the multidrug-resistant K1 strain of P. falciparum with an IC₅₀ value of 0.27 μM.

HY-N1584AR

Halofuginone (hydrobromide) (Standard)	Inhibitor
Halofuginone (hydrobromide) (Standard) is the analytical standard of Halofuginone (hydrobromide). This product is intended for research and analytical applications. Halofuginone (RU-19110) hydrobromid, a Febrifugine derivative, is a competitive prolyl-tRNA synthetase inhibitor with a K_i of 18.3 nM. Halofuginone hydrobromid is a specific inhibitor of type-I collagen synthesis and attenuates osteoarthritis (OA) by inhibition of TGF-β activity. Halofuginone hydrobromid is also a potent pulmonary vasodilator by activating Kv channels and blocking voltage-gated, receptor-operated and store-operated Ca²⁺ channels. Halofuginone hydrobromid has anti-malaria, anti-inflammatory, anti-cancer, anti-fibrosis effects.

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.

HY-13735AR

Quinacrine (dihydrochloride) (Standard)	Inhibitor
Quinacrine (dihydrochloride) (Standard) is the analytical standard of Quinacrine (dihydrochloride). This product is intended for research and analytical applications. Quinacrine (Mepacrine) dihydrochloride is an orally bioavailable antimalarial agent, which possess anticancer effect both in vitro and vivo. Quinacrine dihydrochloride suppresses NF-κB and activate p53 signaling, which results in the induction of the apoptosis.

HY-W774926

Permethrin-d₆	Inhibitor
Permethrin-d₆ (NRDC-143-d₆) is deuterium labeled Permethrin. Permethrin (NRDC-143) is an insecticide, acaricide and a high selectively inhibitor of the Mitochondrial complex I, found in sediment and water samples. Permethrin shows estrogenic in vivo and anti-estrogenic activity in vitro. Permethrin also acts as a neurotoxin affecting neuron membranes by prolonging Sodium channel activation. Permethrin decreases resistance to bacterial infections in medaka (Oryzias latipes).

HY-N7236

Pervicoside B	Inhibitor
Pervicoside B is a glycoside C isolated from Neothyone gibbosa sea cucumber. In vitro studies have shown that Pervicoside B has a potent antiparasitic effect against Leishmania mexicana, inhibiting 100% of promastigotes at 5-10 μg/mL. Pervicoside B also exhibits strong antifungal activity against Aspergillus niger, with MIC values ranging from 4.65 to 16.7 μg/mL. Pervicoside B has potential applications in the inhibition of parasitic infections and fungal diseases.

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Antiparasitic Compound library

Compound library containing all kinds of molecules with anti-parasite activity.

550compounds HY-L082

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