GLUT inhibitor-1 is a potent and orally active inhibitor of glucose transporters, targeting both GLUT1 and GLUT3, with IC 50 s of 242 nM and 179 nM, respectively. GLUT inhibitor-1 has the potential for the reaesrch of cancers and autoimmune diseases.
性状
Solid
IC50 & Target[1][2]
GLUT1 242 nM (IC50) GLUT3 179 nM (IC5
体内研究(In Vivo)
Summary of the pharmacokinetic parameters of GLUT inhibitor-1 (compound 15b; 30 mg/kg) in mouse and rat.
Parameter
Mouse
Rat
oral C max (ng/mL)
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
参考文献
[1]. Liu KG, et al. Discovery and Optimization of Glucose Uptake Inhibitors. J Med Chem. 2020;63(10):5201-5211.
溶解度数据
In Vitro: DMSO : 100 mg/mL (181.93 mM; ultrasonic and warming and heat to 60°C)配制储备液