ChemicalBook--->CAS DataBase List--->209746-59-8

209746-59-8

209746-59-8 Structure

209746-59-8 Structure
IdentificationBack Directory
[Name]

T-1095
[CAS]

209746-59-8
[Synonyms]

T-1095
CS-2245
T 1095; T1095
T1095, T 1095, T1095
1-Propanone, 3-(5-benzofuranyl)-1-[2-hydroxy-6-[[6-O-(methoxycarbonyl)-β-D-glucopyranosyl]oxy]-4-methylphenyl]-
[(2R,3S,4S,5R,6S)-6-{2-[3-(1-benzofuran-5-yl)propanoyl]-3-hydroxy-5-methylphenoxy}-3,4,5-trihydroxyoxan-2-yl]methyl methyl carbonate
[Molecular Formula]

C26H28O11
[MDL Number]

MFCD28404653
[MOL File]

209746-59-8.mol
[Molecular Weight]

516.49
Chemical PropertiesBack Directory
[Boiling point ]

732.3±60.0 °C(Predicted)
[density ]

1.425±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMF: 5 mg/ml,DMSO: 2 mg/ml,Ethanol: 1 mg/ml,PBS (pH 7.2): insol
[form ]

A crystalline solid
[pka]

7.47±0.40(Predicted)
[Appearance]

light yellow solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319
[Precautionary statements ]

P264-P270-P280-P301+P312-P330-P302+P352-P321-P305+P351+P338-P332+P313-P362+P364-P337+P313-P501
Hazard InformationBack Directory
[Uses]

T-1095 is a selective and orally active Na+-glucose cotransporter (SGLT) inhibitor with IC50s of 22.8 μM and 2.3 μM for human SGLT1 and SGLT2, respectively. T-1095 can be used for diabetes research[1].
[in vivo]

T-1095 is absorbed into the circulation via oral administration, is metabolized to the active form, T-1095A, and suppresses the activity of SGLTs in the kidney[1].
Orally administered T-1095 (3-30 mg/kg) increases urinary glucose excretion in diabetic animals, thereby decreasing blood glucose levels[1].
With long-term T-1095 (0.01% or 0.1% T-1095 mixed diet; for 28 days) treatment, both blood glucose and HbA1c levels were reduced in streptozotocin (STZ)-induced diabetic rats and yellow KK mice. In addition, there was amelioration of abnormal carbohydrate metabolism, i.e., hyperinsulinemia and hypertriglyceridemia, and of the development of microalbuminuria, in yellow KK mice[1].

[IC 50]

hSGLT1: 22.8 μM (IC50); hSGLT2: 2.3 μM (IC50)
[References]

[1] A Oku, et al. T-1095, an inhibitor of renal Na+-glucose cotransporters, may provide a novel approach to treating diabetes. Diabetes. 1999 Sep;48(9):1794-800. DOI:10.2337/diabetes.48.9.1794
Spectrum DetailBack Directory
[Spectrum Detail]

T-1095(209746-59-8)1HNMR
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