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1438071-12-5

1438071-12-5 Structure

1438071-12-5 Structure
IdentificationBack Directory
[Name]

N-[(4-chloro-2-methylphenyl)methyl]-1-(4-chlorophenyl)-N-[(5-nitrothiophen-2-yl)methyl]methanamine
[CAS]

1438071-12-5
[Synonyms]

GSK-2945
GSK-2945 (GSK2945 )
GSK 2945 DISCONTINUED. Please see G797405
2-Thiophenemethanamine, N-[(4-chloro-2-methylphenyl)methyl]-N-[(4-chlorophenyl)methyl]-5-nitro-
N-[(4-chloro-2-methylphenyl)methyl]-1-(4-chlorophenyl)-N-[(5-nitrothiophen-2-yl)methyl]methanamine
[Molecular Formula]

C20H18Cl2N2O2S
[MDL Number]

MFCD32204617
[MOL File]

1438071-12-5.mol
[Molecular Weight]

421.34
Chemical PropertiesBack Directory
[Boiling point ]

525.0±45.0 °C(Predicted)
[density ]

1.363±0.06 g/cm3(Predicted)
[solubility ]

Acetonitrile (Slightly), DMSO (Slightly, Heated), Methanol (Slightly, Sonicated)
[form ]

Solid
[pka]

5.23±0.50(Predicted)
[color ]

Off-White to Light Beige
[Stability:]

Hygroscopic
Hazard InformationBack Directory
[Uses]

GSK 2945 is an antagonist with high specificity for REV-ERBα, Nuclear heme receptor reverse erythroblastosis virus, which is known to regulate circadian rhythm and more specifically, regulation of cholesterol 7α-hydroxylase (CYP7A1) and bile acid synthesis.
[in vivo]

GSK2945 (0-10 mg/kg; intraperitoneal injection; twice every day; for 7 days; male C57BL/6 mice) treatment increases hepatic mouse cholesterol 7α-hydroxylase (Cyp7a1) level and lowers plasma cholesterol in wild-type mice[1].

Animal Model:Male C57BL/6 mice (8-10 weeks of age)[1]
Dosage: 0 mg/kg or 10 mg/kg
Administration:Intraperitoneal injection; twice every day; for 7 days
Result:Increased hepatic mouse cholesterol 7α-hydroxylase (Cyp7a1) level and lowered plasma cholesterol in wild-type mice.
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