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1330003-04-7

1330003-04-7 Structure

1330003-04-7 Structure
IdentificationBack Directory
[Name]

CZC-25146 hydrochloride
[CAS]

1330003-04-7
[Synonyms]

CS-1206
CS-1074
CZC-25146.HCl
CZC-25146 hydrochL
CZC-25146 hydrochloride
CZC-25146 hydrochloride >=98% (HPLC)
CZC-25146; CZC 25146; CZC25146;CZC25146 HYDROCHLORIDE;CZC 25146 HYDROCHLORIDE
N-[2-[[5-Fluoro-2-[[2-Methoxy-4-(4-Morpholinyl)phenyl]aMino]-4-pyriMidinyl]aMino]phenyl]-MethanesulfonaMide hydrochloride
CZC-25146.HCL;N-[2-[[5-FLUORO-2-[[2-METHOXY-4-(4-MORPHOLINYL)PHENYL]AMINO]-4-PYRIMIDINYL]AMINO]PHENYL]-METHANESULFONAMIDE HYDROCHLORIDE
[EINECS(EC#)]

604-604-1
[Molecular Formula]

C22H26ClFN6O4S
[MDL Number]

MFCD22417347
[MOL File]

1330003-04-7.mol
[Molecular Weight]

524.996
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C
[solubility ]

DMSO: >15mg/mL (warmed)
[form ]

powder
[color ]

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


GHS06
[Signal word ]

Danger
[Hazard statements ]

H301-H319
[Precautionary statements ]

P301+P310-P305+P351+P338
[Hazard Codes ]

T,Xi
[Risk Statements ]

25-36
[Safety Statements ]

26-45
[RIDADR ]

UN 2811 6.1 / PGIII
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

N-(2-(2-(2-Methoxy-4-morpholinophenylamino)-5-fluoropyrimidin-4-ylamino)phenyl)methanesulfonamide is a compound that acts as an inhibitor of LRRK2, a factor in the expression of Parkinsons’s disease, and is ATP-competitive.
[in vivo]

CZC-25146 (1 mg/kg for i.v.; 5 mg/kg for p.o.; single dosage) exhibits relatively good pharmacokinetic properties and an extensive distribution throughout animal body following intravenous injection into mice[1].
CZC-25146 (250 mg/kg; p.o.; 14 days) reduces the ATZ polymer levels in over expressing human polymeric ATZ mice[3].

Animal Model:Male CD-1 mice[1]
Dosage:1 mg/kg for i.v.; 5 mg/kg for p.o.
Administration:i.v. and p.o.; single dosage
Result:Pharmacokinetic Parameters of CZC-25146 in male CD-1 mice[1].
i.v. (1 mg/kg)p.o. (5 mg/kg)
CL (L/h/kg)2.3
Vss (L/kg)5.4
t1/2 (h)1.61
tmax (h)00.25
Cmax (ng/mL)1541357
AUClast (ng/mL·h)4192878
AUCinf (ng/mL·h)4342894
F (%)133
Animal Model:Genetically modified male mice (6 weeks; over expressing human polymeric ATZ)[3]
Dosage:250 mg/kg
Administration:p.o.; 14 days
Result:Dramatically and reproducibly reduced the ATZ polymer levels with an overall reduction from 60% in the control group to 37%
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