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| Product | Description | |
|---|---|---|
| Amthamine dihydrobromide | ?98% (HPLC), solid. Group: Fluorescence/luminescence spectroscopy. |  |
| Amthamine dihydrobromide | Amthamine dihydrobromide. Group: Biochemicals. Grades: Purified. CAS No. 142457-00-9. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. |  Worldwide |
| Amthamine dihydrobromide | Amthamine dihydrobromide is the dihydrobromide salt of amthamine, which is a highly selective histamine H2 receptor agonist. It is a weak antagonist at H3 and has no activity at H1 receptors. It decreases myogenic tone and induces vasodilation of cerebral arteries in vitro. It can be used in the suppression of the release of serotonin and H2 receptor-mediated eosinophil peroxidase (EPO). It has been used to study the effect of mast cells on T regulatory cell function. Synonyms: 5-(2-Aminoethyl)-4-methylthiazol-2-amine Dihydrobromide; A 4730 Dihydrobromide; 2-Amino-4-methyl-5-thiazoleethanamine dihydrobromide; 2-Amino-5-(2-aminoethyl)-4-methylthiazole dihydrobromide. Grades: ≥99% by HPLC. CAS No. 142457-00-9. Molecular formula: C6H13N3SBr2. Mole weight: 319.06. |  |
| Amthamine dihydrobromide | Amthamine is a histamine receptor (H1R-H4R) agonist. Amthamine can produce liver congestion and necrosis of liver cells. Amthamine can be used to study the induction effect of H1R-H4 agonist on hepatotoxicity [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 142457-00-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-101063. |  |
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