ChemicalBook--->CAS DataBase List--->149654-41-1

149654-41-1

149654-41-1 Structure

149654-41-1 Structure
IdentificationBack Directory
[Name]

U 92016A
[CAS]

149654-41-1
[Synonyms]

U92016A hydrochloride
[Molecular Formula]

C19H26ClN3
[MDL Number]

MFCD00920890
[MOL File]

149654-41-1.mol
[Molecular Weight]

331.89
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

DMF: 5 mg/ml; DMSO: 20 mg/ml; Ethanol: 1 mg/ml; PBS (pH 7.2): 0.1 mg/ml
[form ]

A crystalline solid
Hazard InformationBack Directory
[Uses]

U 92016A is a selective SR-1A agonist.
[Biological Activity]

Selective 5-HT 1A receptor agonist that displays high intrinsic activity (K i values are 0.4, 7.7 and 36 nM for 5-HT 1A , 5-HT 1D and D 2 receptors respectively and > 1000 nM for 5-HT 2 , D 1 , α 1 and α 2 receptors). Produces hypothermia, hypotension and 5-HT behavioral syndrome following p.o. administration.
[in vivo]

U92016A (U-92016A) potently decreases rectal temperature in mice. U92016A also elicits the 5-HT-mediated syndrome in rats and results in a dose-related decrease in 5-hydroxytryptophan accumulation. U92016A also decreases arterial blood pressure in spontaneously hypertensive rats and inhibits sympathetic nerve activity in cats. U92016A displays excellent potency and a long duration of action. U92016A also inhibits the firing of dorsal raphe 5-HT neurons and is active in two social interaction assays. The p.o. bioavailability of U92016A is 45%[2].

[IC 50]

5-HT1A Receptor: 0.2 nM (Ki)
[storage]

Store at -20°C
149654-41-1 suppliers list
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