ChemicalBook--->CAS DataBase List--->2095432-55-4

2095432-55-4

2095432-55-4 Structure

2095432-55-4 Structure
IdentificationBack Directory
[Name]

SR-18292
[CAS]

2095432-55-4
[Synonyms]

SR-18292
SR 18292;SR18292
SR-18292; SR 18292; SR18292
2-Propanol, 1-[(1,1-dimethylethyl)[(4-methylphenyl)methyl]amino]-3-(1H-indol-4-yloxy)-
[Molecular Formula]

C23H30N2O2
[MOL File]

2095432-55-4.mol
[Molecular Weight]

366.5
Chemical PropertiesBack Directory
[Boiling point ]

553.6±50.0 °C(Predicted)
[density ]

1.132±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[solubility ]

DMF: 25 mg/ml; DMSO: 25 mg/ml; DMSO:PBS (pH 7.2) (1:2): 0.33 mg/ml; Ethanol: 10 mg/ml
[form ]

A crystalline solid
[pka]

13.90±0.20(Predicted)
[color ]

White to light brown
[InChIKey]

CMTOYDGVFTZNSM-BTJKTKAUSA-N
[SMILES]

CC(C)(C)N(CC(O)COC1=CC=CC2=C1C=CN2)CC3=CC=C(C)C=C3.O=C(O)/C=C\C(O)=O
Safety DataBack Directory
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

SR 18292 is a novel selective inhibitor of PGC-1alpha Gluconeogenic Activity.
[Biological Activity]

SR-18292 is a potent and specific inhibitor of hepatic gluconeogenesis via increased acetylation of PGC-1α and suppression of gluconeogenic gene expression. SR-18292 reduces blood glucose and increases hepatic insulin sensitivity in mouse models of T2D.
[in vivo]

SR-18292 reduces fasting blood glucose, increases hepatic insulin sensitivity and improves glucose homeostasis in diabetic mice. The high fat diet (HFD) fed mice, a dietary model of obesity and T2D, are treated with SR-18292 (45mg/kg) via I.P. injection for 3 consecutive days and again on day 4 before measuring fasting blood glucose. Strikingly, mice that are treated with SR-18292 have significantly lower levels of fasting blood glucose concentrations compared to matched vehicle-treated control mice. The induction of gluconeogenic gene expression is a regulatory component of the response to fasting. Importantly, gluconeogenic gene expression, specifically that of Pck1, is inhibited in livers isolated from mice treated with SR-18292[1].

Spectrum DetailBack Directory
[Spectrum Detail]

SR-18292(2095432-55-4)1HNMR
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