GNF2133 is a potent, selective and orally active DYRK1A inhibitor with IC 50 s of 0.0062, >50 μM for DYRK1A and GSK3β, respectively. GNF2133 shows good proliferation potency and efficacy on rat and human primary β-cell. GNF2133 significantly improves glucose disposal capacity and increases insulin secretion. GNF2133 has the potential for the research of type 1 diabetes.
性状
Solid
IC50 & Target[1][2]
DYRK1 DYRK1A 0.0062 μM (IC50)
体内研究(In Vivo)
GNF2133 (30 mg/kg; p.o.) shows good oral absorption with oral bioavailability of 22.3%.
GNF2133 (30 mg/kg; p.o.; once a day for 5 days) shows the ability to proliferate β-cells in vivo.
GNF2133 (3, 10, 30 mg/kg) significantly improves glucose disposal capacity and increased insulin secretion in RIP-DTA mice.
Pharmacokinetic Parameters of GNF2133 in CD-1 mice.
plasma (iv)
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 YA, et al. Selective DYRK1A Inhibitor for the Treatment of Type 1 Diabetes: Discovery of 6-Azaindole Derivative GNF2133. J Med Chem. 2020 Mar 26;63(6):2958-2973.
溶解度数据
In Vitro: DMSO : 4 mg/mL (9.21 mM; ultrasonic and warming and heat to 60°C)配制储备液