About 10 results found for searched term "51-41-2" (0.062 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M2038 | Rosiglitazone maleate | PPAR |
| Avandia | ||
| Rosiglitazone maleate (Avandia) is a potent and selective PPARγ ligand that binds to the PPARγ ligand-binding domain with a Kd value of 43 nM. | ||
| M3764 | DY131 | Estrogen Receptor |
| GSK 9089 | ||
| DY131(GSK 9089) is a novel selective agonist of ERRβ and ERRγ which displays minimal activity at ERRα, ERα and ERβ at concentrations up to 30 μM. | ||
| M9264 | Norepinephrine | Adrenergic Receptor |
| Levarterenol; Levophed; Arterenol | ||
| Norepinephrine is generally considered to be a β1-selective adrenergic receptor agonist with EC50 of 5.37 μM. | ||
| M10754 | Avermectin B1 | Anti-infection |
| Abamectin | ||
| Avermectin B1 (Abamectin) is an orally anti-infection agent, which can be used in the research of parasitic worms, insect pests, agriculture and animal husbandry. Avermectin B1 can also induce the production of ROS and induces cytotoxicity, apoptosis and autophagy. | ||
| M14988 | Chikusetsusaponin Iva | Others |
| Calenduloside F | ||
| Chikusetsusaponin IVa a major active ingredient of triterpenoid saponins, exerts antithrombotic effects, including minor hemorrhagic events. | ||
| M20540 | Alrestatin | Others |
| Alrestatin is an inhibitor of aldose reductase which is involved in the pathogenesis of complications of diabetes mellitus, including diabetic neuropathy. | ||
| M24549 | Crenezumab | Amyloid |
| MABT 5102A; RG 7412 | ||
| Crenezumab (MABT 5102A; RG 7412) is a fully humanized anti-Aβ monoclonal antibody that binds multiple forms of Aβ, such as soluble, oligomeric and fibrillar, for use in Alzheimer's disease research. | ||
| M27721 | Nevirapine-d3 | HIV Protease |
| d3 | ||
| Nevirapine-d3 (BI-RG 587-d3) is the deuterium labeled Nevirapine. Nevirapine is a non-nucleoside inhibitor of HIV-1 reverse transcriptase used to treat and prevent HIV/AIDS; with a Ki of 270 μM. | ||
| M56257 | GW-803430 | Others |
| GW-803430 (GW-3430) is a potent and selective melanin-concentrating hormone receptor 1 (MCH R1) antagonist with a pIC50 of 9.3. | ||
| M56052 | Zavondemstat | Histone demethylase |
| Zavondemstat (QC8222; TACH 101) is an inhibitor of histone lysine demethylase 4D (KDM4D) with antineoplastic activity. | ||
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