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Sotagliflozin(LX4211)
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Sotagliflozin(LX4211)图片
CAS NO:1018899-04-1
规格:≥98%
包装与价格:
包装价格(元)
5mg电议
10mg电议
25mg电议
50mg电议
100mg电议
250mg电议
500mg电议

产品介绍
理化性质和储存条件
Molecular Weight (MW)424.94
FormulaC21H25ClO5S
CAS No.1018899-04-1
Storage-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)DMSO: 84 mg/mL (197.7 mM)
Water: <1 mg/mL
Ethanol: 17 mg/mL (40.0 mM)
Other infoChemical Name: (2S,3R,4R,5S,6R)-2-(4-chloro-3-(4-ethoxybenzyl)phenyl)-6-(methylthio)tetrahydro-2H-pyran-3,4,5-triol
InChi Key: QKDRXGFQVGOQKS-CRSSMBPESA-N
InChi Code: InChI=1S/C21H25ClO5S/c1-3-26-15-7-4-12(5-8-15)10-14-11-13(6-9-16(14)22)20-18(24)17(23)19(25)21(27-20)28-2/h4-9,11,17-21,23-25H,3,10H2,1-2H3/t17-,18-,19+,20+,21-/m1/s1
SMILES Code: O[C@@H]([C@@H]([C@H]([C@H](C1=CC=C(Cl)C(CC2=CC=C(OCC)C=C2)=C1)O3)O)O)[C@H]3SC
SynonymsZynquista; LP-80203; LX4211; LP 80203; LX-4211; LP80203; LX 4211
实验参考方法
In Vitro

In vitro activity: LX4211 inhibits [14C]AMG uptake with IC50 of 62.0 nM for mouse SGLT1 and 0.6 nM for mouse SGLT2, respectively.

In VivoIn mice, LX4211 (60 mg/kg, p.o.) reduces intestinal glucose absorption by inhibiting SGLT1, resulting in net increases in GLP-1 and PYY release and decreases in GIP release and blood glucose excursions. In nonobese diabetes-prone mice with type 1 diabetes, Sotagliflozin (30 mg/kg) significantly improves glycemic control, without increasing the rate of hypoglycemia measurements.
Animal modelMale albino C57BL/6-Tyrc-Brd mice
Formulation & DosageDissolved in aqueous 0.1% v/v Tween 80; 60 mg/kg; oral administration.
ReferencesJ Pharmacol Exp Ther. 2013 May;345(2):250-9; Diabetes Metab Syndr Obes. 2015 Feb 26;8:121-7.