Tofogliflozin (hydrate)

(Synonyms: CSG-452 hydrate)
目录号: PL10921 纯度: ≥98%
Tofogliflozin hydrate (CSG-452 hydrate) 是一种有效的,高度特异性的和选择性的 SGLT2 抑制剂,其 IC50 值为 2.9 nM,对人、大鼠和小鼠 SGLT2 的 Ki 值分别为 2.9 nM,14.9 nM 和 6.4 nM。Tofogliflozin hydrate 部分抑制肾小管细胞中高葡萄糖诱导的 ROS 生成。
CAS No. :1201913-82-7
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中文名称
Tofogliflozin (hydrate)
中文别名
奥卡西平N-硫酸盐;托格列净;托格列净一水合物;托格列净一水合物(1:1);Tofogliflozin (hydrate)
英文名称
Tofogliflozin (hydrate)
英文别名
CSG452;Tofogliflozin (USAN);UNII-P8DD8KX4O4;Tofogliflozin [USAN:INN];Tofogliflozin hydrate (JAN);CHEMBL2105711;D09978;(1S,3'R,4'S,5'S,6'R)-6-((4-Ethylphenyl)methyl)-3',4',5',6'-tetrahydro-6'-(hydroxymethyl)- spiro(isobenzofuran-1(3H),2'-(2H)pyran)-3',4',5'-triol monohydrate;(1S,3'R,4'S,5'S,6'R)-6-((4-Ethylphenyl)methyl)-6'-(hydroxymethyl)-3',4',5',6'-tetrahydro- 3H-spiro(2-benzofuran-1,2'-pyran)-3',4',5'-triol monohydrate;(3S,3'R,4'S,5'S,6'R)-5-[(4-ethylphenyl)methyl]-6'-(hydroxymethyl)spiro[1H-2-benzofuran-3,2'-oxane]-3',4',5'-triol;(3S,3'R,4'S,5'S,6'R)-5-[(4-ethylphenyl)methyl]-6'-(hydroxymethyl)spiro[1H-2-benzofuran-3,2'-oxane]-3',4',5'-triol,hydrate;TOFOGLIFLOZIN;Tofogliflozin Hydrate;Tofogliflozin hydrate (1:1);CSG452 hydrate;CSG-452 hydrate;hydrate;(1S,3'R,4'S,5'S,6'R)-6-[(4-Ethylphenyl)methyl]-3',4',5',6'-tetrahydro-6'-(hydroxymethyl)spiro[isobenzofuran-1(3H),2'-[2H]pyran]-3',4',5'-triol hydrate (1:1);Tofogliflozin (hydrate)
Cas No.
1201913-82-7
分子式
C22H26O6.H2O
分子量
404.45
包装储存
Powder -20°C 3 years;4°C 2 years
详情描述
Tofogliflozin hydrate (CSG-452 hydrate) 是一种有效的,高度特异性的和选择性的 SGLT2 抑制剂,其 IC50 值为 2.9 nM,对人、大鼠和小鼠 SGLT2 的 Ki 值分别为 2.9 nM,14.9 nM 和 6.4 nM。Tofogliflozin hydrate 部分抑制肾小管细胞中高葡萄糖诱导的 ROS 生成。
产品详情
Tofogliflozin hydrate (CSG-452 hydrate) 是一种有效的,高度特异性的和选择性的 SGLT2 抑制剂,其 IC50 值为 2.9 nM,对人、大鼠和小鼠 SGLT2 的 Ki 值分别为 2.9 nM,14.9 nM 和 6.4 nM。Tofogliflozin hydrate 部分抑制肾小管细胞中高葡萄糖诱导的 ROS 生成。
生物活性
Tofogliflozin hydrate (CSG-452 hydrate) is a potent and highly specific sodium/glucose cotransporter 2 (SGLT2) inhibitor with an IC 50 of 2.9 nM and K i values of 2.9 nM, 14.9 nM, and 6.4 nM for human, rat, and mouse SGLT2. Tofogliflozin partially inhibits high glucose-induced reactive oxyen species (ROS) generation in tubular cells.
性状
Solid
IC50 & Target[1][2]
IC50: 2.9 nM (SGLT2); Ki: 2.9 nM ( human SGLT2), 14.9 nM (rat SGLT2), and 6.4 nM (mouse SGLT2)
体外研究(In Vitro)
Tofofloxacin (3-30 nM; 24 hours; tubular epithelial cells) treatment inhibits the oxidative stress generation and monocyte chemoattractant protein-1 (MCP-1) gene expression in tubular cells induced by high glucose.
Tofofloxacin (3-30 nM; 8 days; tubular epithelial cells) treatment inhibits the apoptotic cell death induced by high glucose. has not independently confirmed the accuracy of these methods. They are for reference only.RT-PCR
体内研究(In Vivo)
Tofogliflozin (0.1-10 mg/kg; oral administration; once daily; for 4 weeks; db/db mice) treatment improves hyperglycemia and thereby ameliorated glucose intolerance of the obese diabetic mice. has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model:
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
ClinicalTrial
参考文献
[1]. Suzuki M, et al. Tofogliflozin, a potent and highly specific sodium/glucose cotransporter 2 inhibitor, improves glycemic control in diabetic rats and mice. J Pharmacol Exp Ther. 2012 Jun;341(3):692-701.
[2]. Ishibashi Y, et al. Tofogliflozin, A Highly Selective Inhibitor of SGLT2 Blocks Proinflammatory and Proapoptotic Effects of Glucose Overload on Proximal Tubular Cells Partly by Suppressing Oxidative Stress Generation. Horm Metab Res. 2016 Mar;48(3):191-5.
溶解度数据
In Vitro: DMSO : ≥ 100 mg/mL (247.25 mM)H2O : 0.33 mg/mL (0.82 mM; Need ultrasonic)
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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