Combination histamine antagonists

Doxylamine succinate competitively inhibits histamine at H1 receptors with substantial sedative and anticholinergic effects.

Doxylamine succinate competitively inhibits histamine at H1 receptors with substantial sedative and anticholinergic effects.

Doxylamine succinate competitively inhibits histamine at H1 receptors with substantial sedative and anticholinergic effects.

Doxylamine succinate competitively inhibits histamine at H1 receptors with substantial sedative and anticholinergic effects.

Application Famotidine has been used to test its effect on the human ether-a-go-go-related gene (hERG) binding transfected in HEK293 membrane. It has also been used in polycaprolactone based drug delivery studies.

Application Famotidine has been used to test its effect on the human ether-a-go-go-related gene (hERG) binding transfected in HEK293 membrane. It has also been used in polycaprolactone based drug delivery studies.

Famotidine is a histamine H2–receptor antagonist with IC50 of 0.6 mM, commonly used to treat heartburn, GERD, ulcers, and other digestive conditions.A histamine HRH2 antagonist with IC50 of 0.6 mM.

InformationA unique collection of 439 glutamine metabolism related compounds used for high throughput screening (HTS) and high content screening (HCS).Description &amp Advantages•Glutamine metabolism is recognized as a distinctive feature in

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Histamine Diphosphate Monohydrate is potent vasodilater. Endogenous H1 and H2 histamine receptor agonist H1 activation mobilizes Ca2+ H2₂ activation stimulates adenylate cyclase activity in neurons activates nitric oxide synthetase

Histamine Diphosphate Monohydrate is potent vasodilater. Endogenous H1 and H2 histamine receptor agonist H1 activation mobilizes Ca2+ H2₂ activation stimulates adenylate cyclase activity in neurons activates nitric oxide synthetase

Histamine is a neurotransmitter produced by neurons of the posterior hypothalamus. In the brain, histamine is predominantly present in the gray matter.