GNE-207 is a potent, selective and orally bioavailable inhibitor of the bromodomain of CBP, with an IC 50 of 1 nM, exhibits a selectively index of?>2500-fold against BRD4 (1). GNE-207 shows excellent CBP potency, with an EC 50 of 18 nM for MYC expression in MV-4-11 cells.
性状
Solid
IC50 & Target[1][2]
BRD4(1) 3.1 μM (IC50) CBP 1 nM (IC50
体外研究(In Vitro)
GNE-207 is a potent, selective and orally bioavailable inhibitor of the bromodomain of CBP, with an IC50 of 1 nM, a selectively index of?>2500-fold against BRD4 (1) (IC50, 3.1 μM).GNE-207 shows excellent CBP potency, with an EC50 of 18 nM for MYC expression in MV-4-11 cells. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
GNE-207 (5?mg/kg) shows moderate clearance in PK, with acceptable oral bioavailability. has not independently confirmed the accuracy of these methods. They are for reference only.
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]. Lai KW, et al. Design and synthesis of a biaryl series as inhibitors for the bromodomains of CBP/P300. ioorg Med Chem Lett. 2018 Jan 1;28(1):15-23.
溶解度数据
In Vitro: DMSO : 200 mg/mL (391.70 mM; Need ultrasonic)配制储备液