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Histamine receptor ligand
BML-NH100-0005 5 mg 86.00 USD
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Highly selective histamine H2 agonist, devoid of stimulatory activity at H1 and H3 receptors. It induces a dose-dependent increase in gastric acid secretion and is a superior alternative to other H2 agonists for the study of gastric acid secretion.

Product Specification

Alternative Name:2-Amino-5-(2-aminoethyl)-4-methylthiazole . 2HBr
Purity:≥99% (HPLC)
Appearance:Cream crystalline solid
Solubility:Soluble in water.
Long Term Storage:-20°C
BML-NH100 structure
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BML-NH100 structure

Product Literature References

In vitro cardiac pharmacology of the new histamine H2-receptor agonist amthamine: comparisons with histamine and dimaprit: E. Poli, et al.; Agents Actions 40, 44 (1993), Abstract;
The new potent and selective histamine H2 receptor agonist amthamine as a tool to study gastric secretion: G. Coruzzi, et al.; Nauyn Schmeidebergs Arch. Pharmacol. 348, 77 (1993), Abstract;
Histamine H2-receptor agonists. Synthesis, in vitro pharmacology, and qualitative structure-activity relationships of substituted 4- and 5-(2-aminoethyl)thiazoles: J. C. Eriks, et al.; J. Med. Chem 35, 3239 (1992), Abstract;

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