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MSDC-0602
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。
MSDC-0602图片
CAS NO:1133819-87-0
包装与价格:
包装价格(元)
Free Sample (0.1-0.5mg)电议
10mM (in 1mL DMSO)电议
5mg电议
10mg电议
50mg电议
100mg电议
200mg电议
500mg电议

产品介绍
MSDC-0602 (MSDC-0602),一种 PPARγ;-保留噻唑烷二酮 (TZD),与线粒体丙酮酸载体 (MPC) 相互作用并抑制其活性,并具有降低 PPARγ 风险的 2 型糖尿病研究的潜力;-介导的一侧效果。
Cas No.1133819-87-0
别名MSDC-0602
Canonical SMILESO=C1C(SC(N1)=O)CC2=CC=C(OCC(C3=CC(OC)=CC=C3)=O)C=C2
分子式C19H17NO5S
分子量371.41
溶解度DMSO: 125 mg/mL (336.56 mM); Water:< 0.1 mg/mL (insoluble)
储存条件Store at -20°C
General tipsFor obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.
Shipping ConditionEvaluation sample solution : ship with blue ice
All other available size: ship with RT , or blue ice upon request
产品描述

MSDC-0602, a PPARγ-sparing thiazolidinedione (TZD), interacts with the mitochondrial pyruvate carrier (MPC) and inhibits its activity and are effective for treatment of type 2 diabetes with reducing risk of PPARγ-mediated side effects[1][2].

[1]. Chen Z, et al. Resistance and metabolic derangements in obese mice are ameliorated by a novel peroxisome proliferator-activated receptor γ-sparing thiazolidinedione. J Biol Chem. 2012 Jul 6;287(28):23537-48. [2]. Vigueira PA, et al. The beneficial metabolic effects of sensitizers are not attenuated by mitochondrial pyruvate carrier 2 hypomorphism. Exp Physiol. 2017 Aug 1;102(8):985-999.