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487051-12-7

487051-12-7 Structure

487051-12-7 Structure
IdentificationBack Directory
[Name]

N-[3-[1-[[4-(3,4-Difluorophenoxy)phenyl]methyl]-4-piperidinyl]-4-methylphenyl]-2-methylpropanamidehydrochloride
[CAS]

487051-12-7
[Synonyms]

SNAP-94847
SNAP-94847 >=98% (HPLC)
SNAP 94847 hydrochloride
N-[3-[1-[[4-(3,4-Difluorophenoxy)phenyl]methyl]-4-piperidinyl]-4-methylphenyl]-2-methyl-propanamide
Propanamide, N-[3-[1-[[4-(3,4-difluorophenoxy)phenyl]methyl]-4-piperidinyl]-4-methylphenyl]-2-methyl-
N-[3-[1-[[4-(3,4-Difluorophenoxy)phenyl]methyl]-4-piperidinyl]-4-methylphenyl]-2-methylpropanamidehydrochloride
[Molecular Formula]

C29H32F2N2O2
[MOL File]

487051-12-7.mol
[Molecular Weight]

478.57
Chemical PropertiesBack Directory
[storage temp. ]

Desiccate at RT
[solubility ]

DMSO: soluble20mg/mL, clear
[form ]

powder
[color ]

white to beige
Safety DataBack Directory
[Symbol(GHS) ]


GHS09
[Signal word ]

Warning
[Hazard statements ]

H410
[Precautionary statements ]

P273-P501
[Hazard Codes ]

N
[Risk Statements ]

50/53
[Safety Statements ]

60-61
[RIDADR ]

UN 3077 9 / PGIII
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

SNAP 94847 Hydrochloride is an MCH1 antagonist.
[Biological Activity]

SNAP-94847 is a potent antagonist of the melanin-concentrating hormone receptor MCHR-1. SNAP-94847 displays anxiolytic and antidepressant activityand reduces food intake in mice.
[in vivo]

SNAP 94847 (oral gavage; 20 mg/kg; 14 days) shows an exaggerated locomotor response to acute quinpirole [treatment: F(2,19)=11.31, treatment × time: F(34,323) = 4.061], the effect of SNAP 94847 on quinpirole-evoked ambulations over the entire observation period is significant compared to the untreated animals[2]. SNAP 94847 (oral administration; 20 mg/kg; 21 days) in drink water, produces a significant increase in ambulation relative to untreated animals [treatment: F(3,28) = 8.971; treatment × time: F(51,476)=11.50]. shows a marked increase in locomotion is apparent after 40 min in the SNAP 94847-treated group,this effect is significant over 180 min[2]. SNAP 94847 (oral administration; 10 mg/kg), has a good bioavailability (59%), low plasma and blood clearances of 4.2 L/hr/kg and 3.3 L/hr/kg, respectively, and the half-life was shown to be 5.2 h in rats in a PK study[3].

Animal Model:Rat[2]
Dosage:20?mg/kg
Administration:Oral administration; 20?mg/kg; 14 days
Result:Exhibited a exaggerated locomotor response to acute quinpirole.
Animal Model:Rat (PK study)[3]
Dosage:10 mg/kg
Administration:oral gavage; 10 mg/kg
Result:Exhibited good physicochemical properties in rats.
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