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2319790-07-1

2319790-07-1 Structure

2319790-07-1 Structure
IdentificationBack Directory
[Name]

H3R antagonist 1 hydrochloride
[CAS]

2319790-07-1
[Synonyms]

H3R antagonist 1 hydrochloride
[Molecular Formula]

C19H23N3O3.ClH
[MOL File]

2319790-07-1.mol
[Molecular Weight]

377.87
Chemical PropertiesBack Directory
[form ]

Solid
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

H3R antagonist 1 hydrochloride is a histamine receptor 3 (H3R) inverse agonist extracted from patent WO2013107336A1, compound example 2.
[in vivo]

The ability of H3R antagonist 1 hydrochloride-1 to enhance in vivo remyelination is determined with the Cuprizone/Rapamycin-induced demyelination model. Mice are treated with Cuprizone diet combined with intraperitoneal injections of Rapamycin for 5 weeks followed by 9 days of compound administration. Cuprizone diet plus intraperitoneal injections of Rapamycin induced severe demyelination in both corpus callosum and cortex and treatment with H3R antagonist 1 hydrochloride (30 mg/kg, 9 days) significantly increases density of myelin specific Black-gold II staining in the lesion of corpus callosum and cortex in forebrain, compared to vehicle control group[1].

[IC 50]

H3 receptor
[References]

[1] WANG, Rong, et al. THERAPEUTIC USES. WO2013107336A1.
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