ChemicalBook--->CAS DataBase List--->1103500-20-4

1103500-20-4

1103500-20-4 Structure

1103500-20-4 Structure
IdentificationBack Directory
[Name]

LY-2562175
[CAS]

1103500-20-4
[Synonyms]

CS-2847
LY-2562175
1H-Indole-3-carboxylic acid, 6-[4-[[5-cyclopropyl-3-(2,6-dichlorophenyl)-4-isoxazolyl]methoxy]-1-piperidinyl]-1-methyl-
[Molecular Formula]

C28H27Cl2N3O4
[MDL Number]

MFCD30738721
[MOL File]

1103500-20-4.mol
[Molecular Weight]

540.44
Chemical PropertiesBack Directory
[Boiling point ]

740.1±60.0 °C(Predicted)
[density ]

1.48±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMF: 20 mg/ml; DMSO: 30 mg/ml; DMSO:PBS (pH 7.2) (1:3): 0.25 mg/ml
[form ]

A crystalline solid
[pka]

3.43±0.10(Predicted)
Hazard InformationBack Directory
[Description]

LY2562175 is a farnesoid X receptor (FXR) agonist (EC50 = 193 nM in a reporter assay). It is selective for FXR over the glucocorticoid, androgen, mineralocorticoid, and progesterone receptors in HEK293 cells overexpressing the human receptors (EC50s = >10 μM for all in a radioligand binding assay). LY2562175 increases the interaction between FXR and steroid receptor coactivator 1 (SRC-1) with an EC50 value of 121 nM in a cell-free assay. It reduces plasma triglyceride and total cholesterol levels in LDL receptor-null mice (ED50s = 3.4 and 2 mg/kg, respectively). LY2562175 also decreases plasma LDL and increases HDL levels in Zucker diabetic fatty (ZDF) rats when administered at doses of 3, 10, and 30 mg/kg for nine days.
[Uses]

LY2562175, is a potent and selective FXR agonist with an EC50 of 193 nM.
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