MK-8245

    
≥98%

MK-8245

源叶(MedMol)
S80036 一键复制产品信息
1030612-90-8
C17H16BrFN6O4
467.26
5-[3-[4-(2-溴-5-氟苯氧基)-1-哌啶基]-5-异恶唑基]-2H-四氮唑-2-乙酸;CS-0410; (5-{3-[4-(2-bromo-5-fluorophenoxy)piperidin-1-yl]isoxazol-5-yl}-2H-tetrazol-2-yl)acetic acid; (5-{3-[4-(2-bromo-5-fluorophenoxy)piperidin-1-yl]
货号 规格 价格 上海 北京 武汉 南京 购买数量
S80036-5mg ≥98% ¥452.00 >10 - - -
S80036-10mg ≥98% ¥650.00 >10 - - -
S80036-50mg ≥98% ¥2104.00 >10 - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品

产品介绍

MK-8245 is a potent, liver-targeted stearoyl-CoA desaturase (SCD) inhibitor, with IC50s of 1 nM for human SCD1 and 3 nM for both rat SCD1 and mouse SCD1, with antidiabetic and antidyslipidemic efficacy

产品描述: MK-8245 is a potent, liver-targeted stearoyl-CoA desaturase (SCD) inhibitor, with IC50s of 1 nM for human SCD1 and 3 nM for both rat SCD1 and mouse SCD1, with antidiabetic and antidyslipidemic efficacy
靶点: IC50: 1 nM (human SCD1), 3 nM (rat SCD1), 3 nM (mouse SCD1);Dehydrogenase;Stearoyl-CoADesaturase(SCD)
体内研究: MK-8245 (10mg/kg; p.o.) exhibits a tissue distribution profile concentrated in the liver, with low exposure in tissues associated with potential adverse events in rats, dogs, and rhesus monkeys. MK-8245 improves glucose clearance in a dose-dependent manner in eDIO mice administrated before the glucose challenge
参考文献: 1. Oballa RM, et al. Development of a liver-targeted stearoyl-CoA desaturase (SCD) inhibitor (MK-8245) to establish a therapeutic window for the treatment of diabetes and dyslipidemia.J Med Chem. 2011 Jul 28;54(14):5082-96. Epub 2011 Jun 28.
溶解性: Soluble  in  DMSO
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.14 ml 10.701 ml 21.401 ml
5 mM 0.428 ml 2.14 ml 4.28 ml
10 mM 0.214 ml 1.07 ml 2.14 ml
50 mM 0.043 ml 0.214 ml 0.428 ml
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参考文献

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