ChemicalBook--->CAS DataBase List--->1345982-69-5

1345982-69-5

1345982-69-5 Structure

1345982-69-5 Structure
IdentificationBack Directory
[Name]

GSK 2330672
[CAS]

1345982-69-5
[Synonyms]

CS-2639
Iinerixibat
linerixibat
GSK 2330672
GSK 2330672; GSK-2330672
Pentanedioic acid, 3-((((3R,5R)-3-butyl-3-ethyl-2,3,4,5-tetrahydro-7-methoxy-1,1-dioxido-5-phenyl-1,4-benzothiazepin-8-yl)methyl)amino)-
3-[[(3R,5R)-3-butyl-3-ethyl-7-methoxy-1,1-dioxo-5-phenyl-4,5-dihydro-2H-1λ6,4-benzothiazepin-8-yl]methylamino]pentanedioic acid
[EINECS(EC#)]

604-604-1
[Molecular Formula]

C28H38N2O7S
[MDL Number]

MFCD28386358
[MOL File]

1345982-69-5.mol
[Molecular Weight]

546.68
Chemical PropertiesBack Directory
[Boiling point ]

730.8±60.0 °C(Predicted)
[density ]

1.218±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMF: 5 mg/ml; DMSO: 2 mg/ml; PBS (pH 7.2): 0.2 mg/ml
[form ]

A crystalline solid
[pka]

3.27±0.10(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07,GHS09
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335-H401-H411
[Precautionary statements ]

P261-P264-P270-P271-P273-P280-P301+P312-P330-P302+P352-P321-P304+P340-P305+P351+P338-P332+P313-P362+P364-P337+P313-P391-P403+P233-P405-P501
Hazard InformationBack Directory
[Description]

GSK2330672 is an inhibitor of the apical sodium-dependent bile acid transporter (ASBT; IC50s = 42, 2.1, and 1.9 nM for human, mouse, and rat ASBT, respectively). In vivo, GSK2330672 (0.05 mg/kg) stimulates fecal bile acid secretion, reduces hemoglobin A1c (HbA1c) and plasma glucose levels, and increases total GLP-1 (Item No. 24460) and plasma insulin in Zucker diabetic fatty (ZDF) rats.
[storage]

Store at -20°C
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