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ChemicalBook--->CAS DataBase List--->126411-39-0

126411-39-0

126411-39-0 Structure

126411-39-0 Structure
IdentificationBack Directory
[Name]

SR 12813
[CAS]

126411-39-0
[Synonyms]

GW485801
GW-485801
GW 485801
SR12813;SR 12813
SR-12813(GW 485801)
SR-12813;SR12813;SR 12813;GW 485801;GW-485801;GW485801
[[3,5-Bis(1,1-dimethylethyl)-4-hydroxyphenyl]ethenylidene]bis-phosphonicacidtetraethylester
Phosphonic acid, P,P'-[[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]ethenylidene]bis-, P,P,P',P'-tetraethyl ester
[Molecular Formula]

C24H42O7P2
[MDL Number]

MFCD00888473
[MOL File]

126411-39-0.mol
[Molecular Weight]

504.53
Chemical PropertiesBack Directory
[Melting point ]

119-121℃
[Boiling point ]

552.6±50.0 °C(Predicted)
[density ]

1.117±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

DMSO: ≥10 mg/mL
[form ]

solid
[pka]

9.95±0.70(Predicted)
[color ]

White to off-white
Safety DataBack Directory
[WGK Germany ]

3
[HS Code ]

29319090
Hazard InformationBack Directory
[Uses]

SR 12813 is a pregnane X receptor (PXR, NR 112) agonist.
[Definition]

ChEBI: An organic phosphonate that is the tetraethyl ester of [2-(3,5-di-tert-butyl-4-hydroxyphenyl)ethene-1,1-diyl]bis(phosphonic acid).
[Biological Activity]

Pregnane X receptor (PXR) agonist (EC 50 values are 200 and 700 nM for human and rabbit PXR respectively). Activates the farnesoid X receptor (FXR) at μ M concentrations. Displays hypocholesterolaemic activity via enchanced degradation of HMG-CoA reductase.
[Biochem/physiol Actions]

SR-12813 is a 1,1-bisphosphonate ester that exhibits hypocholesterolemic activity. It decreases the biosynthesis of cholesterol by enhancing the degradation of HMG-CoA reductase.
[storage]

Store at +4°C
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