ChemicalBook--->CAS DataBase List--->120635-25-8

120635-25-8

120635-25-8 Structure

120635-25-8 Structure
IdentificationBack Directory
[Name]

Mofegiline hydrochloride
[CAS]

120635-25-8
[Synonyms]

CS-1216
MDL72974A
Mofegiline HCl
Mofegiline hydrochloride
Mofegiline-hydrochloride, MDL72974A
[Molecular Formula]

C11H13F2N.ClH
[MDL Number]

MFCD00890215
[MOL File]

120635-25-8.mol
[Molecular Weight]

233.688
Chemical PropertiesBack Directory
[Melting point ]

131°
[storage temp. ]

Inert atmosphere,2-8°C
[solubility ]

Water: 30 mg/ml
[form ]

Powder
[color ]

White to off-white
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Uses]

Antiparkinsonian.
[in vivo]

Mofegiline hydrochloride (MDL72974A) (0.1-2.5 mg/kg; p.o.; single dose) inhibits MAO-B activity external vivo in rat model and (1.25 mg/kg; i.p.; 18 hours prior to MPTP treatment) exerts its ability to block MPTP neurotoxicity in mice model[1].

Animal Model:Male Sprague-Dawley rats (150-400 g)[1]
Dosage:Group 1: 0.1-2.5 mg/kg; Group 2: 0.05-5 mg/kg
Administration:Oral gavage; single dose for group 1, as for group 2, once daily for 14 days
Result:Showed the inhibition effect on rat brain MAO-A and MAO-B with EC50s of 8 mg/kg and 0.18 mg/kg, respectively, in group 1.
Resulted more potent efficacy on MAO-A inhibition in a daily dosed-manner (group 2) than single dose (group 1) manner, indicating a long half-life of Mofegiline hydrochloride.
Animal Model:Mate SwissWebster (CF-W) mice (25-30 g)[1]
Dosage:1.25 mg/kg
Administration:Intraperitoneal injection; 18 hours prior to administration of MPTP (20 mg/kg; i.p.; 4 times for two-hourly intervals, for 8 days)
Result:Rescued MPTP-induced decreases in striatal levels of dopamine (DA), dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA) in mice.
Animal Model:Male Sprague-Dawley rats (150-400 g) injected with Tyramine (HY-W007606) (1.25-80 μg/kg; i.v.)[1]
Dosage:Group 1: 1.8, 9 mg/kg; Group 2: 0.1, 1 mg/kg
Administration:Oral gavage; single dose for group 1, as for group 2, once daily for 14 days
Result:Did not significantly potentiate the cardiovascular effects of intraduodenally administered Tyramine (HY-W007606) in anaesthetised rats.
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