About 7 results found for searched term "51-74-1" (0.119 seconds)
Cat.No. | Name | Target |
---|---|---|
M2006 | Safinamide Mesylate | Monoamine Oxidase |
FCE28073, PNU-151774E, NW-1015 | ||
Safinamide is a highly selective and reversible monoamine oxidase type B (MAO-B) inhibitor. | ||
M2755 | Histamine Phosphate | Histamine Receptor |
Histamine diphosphate | ||
Histamine Phosphate is an endogenous ligand for the histamine receptor that can induce allergic reactions by acting with H1 receptors, promote acid secretion by acting with H2 receptors, and inhibit histamine release and modulate immune responses by acting with H3 receptors and H4 receptors. It can be used in studies related to allergy, hyperacidity, sleep disorders, asthma and many other diseases. | ||
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. | ||
M40288 | Curculigoside C | Others |
Curculigoside C is a phenolic glucoside with potent antioxidative and neuroprotective activities. Curculigoside C shows IC50 values of 0.25 mM and 0.88 mM for hydroxyl radicals and superoxide anion radicals, respectively. | ||
M7539 | AS1517499 | STAT |
AS1517499 is a novel and potent STAT6 inhibitor with an IC50 value of 21 nM. | ||
M8758 | GW806742X | Necroptosis |
GW806742X is an ATP site-targeing kinase inhibitor (IC50 in nM = 2/VEGFR2, 15/SRC, 47/C-FMS, 851/GSK3, 9016/ERBB2, 9120/FGFR) with potent antiproliferation activity against cancer cultures (IC50 in nM = 5/HUVEC-v, 424/HUVEC-b, 81/HEF, 453/MDA468, 470/A375P, 693/HT29, 734/PC3), GW806742X is now better known as Compound 1 for its anti-necroptosis activity via affinity interaction with ML | ||
M56181 | Sonepiprazole | Dopamine Receptor |
Sonepiprazole (PNU-101387G) is a selective D4 dopamine antagonist with Kis of 3.6, 10.1, 5147, and 7430 nM for rD4-Dopamine, hD4.2-Dopamine, rD2-Dopamine, and Histamine-H1 receptors, respectively. |
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