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1632118-70-7

1632118-70-7 Structure

1632118-70-7 Structure
IdentificationBack Directory
[Name]

BAR 501 impurity
[CAS]

1632118-70-7
[Synonyms]

BAR 501 impurity
(3alpha,5beta,6beta,7alpha)-6-Ethylcholane-3,7,24-triol
(3R,5S,6S,7R,8S,9S,10S,13R,14S,17R)-6-ethyl-17-[(2R)-5-hydroxypentan-2-yl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-3,7-diol
[Molecular Formula]

C26H46O3
[MDL Number]

MFCD30747751
[MOL File]

1632118-70-7.mol
[Molecular Weight]

406.64
Chemical PropertiesBack Directory
[Boiling point ]

527.6±25.0 °C(Predicted)
[density ]

1.047±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMF: 20 mg/mL; DMSO: 100μg/ml; Ethanol: 2 mg/mL; Ethanol:PBS (pH 7.2)(1:2): 500μg/ml
[form ]

A crystalline solid
[pka]

14.82±0.70(Predicted)
Hazard InformationBack Directory
[Description]

BAR501 impurity is an impurity found in the preparation of BAR501 that acts as an agonist of the G protein-coupled bile acid-activated receptor (GP-BAR1). BAR501 impurity (10 μM) induces a 150% increase in luciferase activity in a GP-BAR1 reporter gene assay.1
[Uses]

(3α, 5β, 6β, 7α)-BAR501 (BAR504-6b) is a compound having cholane scaffolds of formula. (3α, 5β, 6β, 7α)-BAR501 can be used for the research of FXR and TGR5/GPBAR1 mediated diseases[1].
[References]

1. Festa, C., Renga, B., D'Amore, C., et al. Exploitation of cholane scaffold for the discovery of potent and selective farnesoid X receptor (FXR) and G-protein coupled bile acid receptor 1 (GP-BAR1) ligands J. Med. Chem. 57(20),8477-8495(2014).
Spectrum DetailBack Directory
[Spectrum Detail]

BAR 501 impurity(1632118-70-7)1HNMR
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