Identification | Back Directory | [Name]
SR 57227 HYDROCHLORIDE | [CAS]
77145-61-0 | [Synonyms]
cm57227 sr57227a CM-57277 SR57227HCl SR 57227 HYDROCHLORIDE SR 57227A HYDROCHLORIDE 1-(6-CHLORO-2-PYRIDINYL)-4-PIPERIDINAMINE HYDROCHLORIDE 4-AMINO-1-(6-CHLORO-2-PYRIDYL)-PIPERIDINE HYDROCHLORIDE 1-(6-chloropyridin-2-yl)piperidin-4-amine hydrochloride 1-(6-chloro-2-pyridinyl)-4-piperidinaminmonohydrochloride 4-amino-1-(6-chloro-2-pyridyl)piperidinemonohydrochloride 1-(6-chloro-2-pyridinyl)-4-piperidinaminemonohydrochloride | [Molecular Formula]
C10H15Cl2N3 | [MDL Number]
MFCD01756430 | [MOL File]
77145-61-0.mol | [Molecular Weight]
248.15 |
Hazard Information | Back Directory | [Uses]
SR 57227A acts as highly potent and shows high affinity for the 5-HT3 receptor agonist. | [Biological Activity]
A high affinity, selective 5-HT 3 receptor agonist, active in vivo and CNS penetrant. | [in vivo]
SR 57227A (1-30 mg/kg; i.p.) dose-dependently reduces immobility time in the forced swimming test with an ED50 value for this effect of 14.2 mg/kg[2].
In the forced swimming test, SR 57227A dose-dependently reduces the duration of immobility in rats after i.p. administration. (ED50=7.6 mg/kg i.p. in rats.) SR 57227A is also active in both species after oral administration. In a time-course study in mice, SR 57227A (20 mg/kg p.o.) produces a significant effect lasting 6 hours. SR 57227A (1 and 3 mg/kg i.p.) reduces the elevation of the escape failures in the learned helplessness model in rats by 50-60% on the last two days of the avoidance task, and reduces isolation-induced aggressivity in mice by 50 to 85%, an effect which is antagonised by Zacopride (1 mg/kg i.p.)[2]. | [storage]
Store at RT |
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Energy Chemical
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