Cat.No. | Name | Information |
---|---|---|
M3209 | Oxfendazole | Oxfendazole is the sulfoxide form of fenbendazole which is a broad spectrum benzimidazole anthelmintic. |
M5841 | Oxibendazole | Obendazole is a class of benzimidazole compounds that interfere with metabolic pathways and are used to protect horses and some domestic pets from infections with roundworms, strongyworms, pinworms and lungworms. |
M5819 | Nitromide | Nitromide is an anti-parasitic agent. |
M5790 | Milbemycin oxime | Milbemycin oxime is a veterinary drug from the group of milbemycins, used as a broad spectrum antiparasitic. |
M5691 | Hexylresorcinol | Hexylresorcinol is an organic compound with local anaesthetic, antiseptic and anthelmintic properties, is a potent inhibitor of mushroom tyrosinase. The IC50 values of hexylresorcinol for monophenolase is 1.24 μM and for diphenolase is 0.85 μM. |
M5606 | Eflornithine hydrochloride hydrate | Eflornithine (DFMO; Difluoromethylornithine) hydrochloride hydrate inhibits polyamine biosynthesis by the selective, irreversible inhibition of ornithine decarboxylase (ODC). A chemoprotective agent that blocks angiogenesis. Its biological half-life is 8 hours. |
M5582 | Dinitolmide | Dinitolmide is a fodder additive for poultry, used to prevent coccidiosis infections. |
M5573 | Diethylcarbamazine citrate | Diethylcarbamazine citrate is an inhibitor of arachidonic acid metabolism in filarial microfilaria; is highly specific for several parasites and does not contain any toxic metallic elements. |
M5571 | Diclazuril | Diclazuril is an anti-coccidial drug. |
M5556 | DEET | DEET is the most common active ingredient in insect repellents. It is intended to provide protection against mosquitoes, ticks, fleas, chiggers, leeches, and many other biting insects. |
M5539 | Crotamiton | Crotamiton is a drug that is used both as a scabicidal (for treating scabies) and as a general antipruritic. It is a prescription lotion based medicine that is applied to the whole body to get rid of the scabies parasite. |
M5529 | Clofentezine | Clofentezine, a growth inhibitor, has sublethal effects on life-table parameters of Tetranychus urticae Koch females. |
M5452 | Bephenium hydroxynaphthoate | Bephenium hydroxynaphthoate is an anthelmintic agent formerly used in the treatment of hookworm infections and ascariasis; B-type AChR activator. |
M5451 | Benzyl benzoate | Benzyl benzoate is an orally active anti-scabies agent, acaricide (EC50= 0.06 g/m2) and fungicide. Benzyl benzoate is an angiotensin II (Ang II) inhibitor with antihypertensive effects. |
M5421 | Artemotil | Artemotil (β-Arteether) has antimalarial activity for the treatment of chloroquine-resistant Plasmodium falciparum malaria with an IC50 of 1.61 nM. Artemotil also has central nervous system (CNS) neurotoxicity and anorectic toxicity in rats, dogs and monkeys. |
M5132 | Quinacrine Dihydrochloride Dihydrate | Quinacrine Hydrochloride Hydrate (Mepacrine Hydrochloride) is an antimalarial that has anti-tumor effects in vivo and in vitro. Quinacrine hydrochloride hydrate inhibits NF-κB, activates p53 signal transduction and induces apoptosis in tumor cells. |
M5021 | Dinotefuran | Dinotefuran is an insecticide of the neonicotinoid class, its mechanism of action involves disruption of the insect's nervous system by inhibiting nicotinic acetylcholine receptors. |
M4991 | Dihydroartemisinin | Dihydroartemisinin is a potent anti-malaria agent. Dihydroartemisinin, a derivative of artemisinin in which the C-10 lactone group is replaced by hemiacetals and active metabolites of all artemisinin compounds, is a widely used antimalarial compound that effectively induces iron death in acute myeloid leukemia cells (HL60, KG1, and THP-1) by regulating iron metabolism. |
M4910 | Secnidazole | Secnidazole (flagellate) is a nitroimidazoles anti - infective compound. |
M4892 | GNF179 | GNF179 is an optimized 8,8-dimethyl IP analog that exhibited the potency(4.8 nM against the multidrug resistant strain W2). |
M4886 | Selamectin | Selamectin is an antiparasitic agent and insect repellent that activates glutamate-gated chloride channels in neurons and pharyngeal muscles to prevent filariasis, lymphatic filariasis and nematode infection. Selamectin is also an effective p-glycoprotein substrate and inhibitor with IC50 of 120 nM. |
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