CAS NO: | 666842-36-0 |
生物活性 | KGA-2727 is a first selective, high-affinity and orally activeSGLT1inhibitor withKis of 97.4 nM and 43.5 nM forhumanandratSGLT1, respectively. The selectivity ratios (Kifor SGLT2/KiforSGLT1) of KGA-2727 are 140 (human) and 390 (rat). KGA-2727 has antidiabetic efficacy[1]. | ||||||||||||||||
IC50& Target | Ki: 97.4 nM (human SGLT1), 43.5 nM (rat SGLT1)[1] | ||||||||||||||||
体外研究 (In Vitro) | A Dixon plot analysis for KGA-2727 displays good linearity for human SGLT1 and SGLT2. The results of the Dixon plot show that KGA-2727 inhibits these SGLTs in a competitive manner. KGA2727 dose-dependently inhibits Methyl-Dglucopyranoside (AMG) uptake by SGLT1 and SGLT2[1]. | ||||||||||||||||
体内研究 (In Vivo) | In the oral glucose tolerance test with streptozotocin-induced diabetic rats, KGA-2727 attenuates the elevation of plasma glucose after glucose loading, indicating that KGA-2727 improves postprandial hyperglycemia[1]. | ||||||||||||||||
分子量 | 536.62 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C26H40N4O8 | ||||||||||||||||
CAS 号 | 666842-36-0 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 | 4°C, protect from light *In solvent : -80°C, 6 months; -20°C, 1 month (protect from light) | ||||||||||||||||
溶解性数据 | In Vitro: DMSO : 100 mg/mL(186.35 mM;Need ultrasonic) H2O : 20 mg/mL(37.27 mM;ultrasonic and warming and heat to 60℃) 配制储备液
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以下溶剂前显示的百
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