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1639895-85-4

中文名称 1639895-85-4
英文名称 tBID
CAS 1639895-85-4
分子式 C11H3Br4N3O2
分子量 528.78
MOL 文件 1639895-85-4.mol
更新日期 2024/06/20 21:07:20
1639895-85-4 结构式 1639895-85-4 结构式

基本信息

中文别名
HIPK2抑制剂(TBID)
英文别名
tBID
1H-Isoindole-1,3(2H)-dione, 4,5,6,7-tetrabromo-2-(1H-imidazol-2-yl)-

物理化学性质

沸点724.9±70.0 °C(Predicted)
密度2.604±0.06 g/cm3(Predicted)
储存条件-20°C储存
溶解度DMSO: 26 mg/mL (49.17 mM and warming)
酸度系数(pKa)12.01±0.10(Predicted)
形态Solid
颜色Light yellow to yellow

安全数据

危险性符号(GHS)
GHS07
警示词警告
危险性描述H302-H315-H319-H335
1639895-85-4价格(试剂级)
报价日期产品编号产品名称CAS号包装价格
2024/08/19HY-1004641639895-85-4
tBID
1639895-85-41mg1100元
2024/08/19HY-1004641639895-85-4
tBID
1639895-85-45mg2850元
2024/08/19HY-1004641639895-85-4
tBID
1639895-85-410mM * 1mLin DMSO3315元

常见问题列表

生物活性
tBID 是同源结构域相互作用蛋白激酶2 (HIPK2) 的选择性抑制剂,IC50值为 0.33 μM。
靶点

IC50: 0.33 µM (HIPK2)

体外研究

Homeodomain-interacting protein kinase 2 (HIPK2) is a Ser/Thr kinase controlling cell proliferation and survival. TBID, displays toward HIPK2 unprecedented efficacy (IC 50 =0.33 µM) and selectivity (Gini coefficient 0.592 out of a panel of 76 kinases). The two other members of the HIPK family, HIPK1 and HIPK3, are also inhibited by TBID albeit less efficiently than HIPK2. The mode of action of TBID is competitive with respect to ATP, consistent with modelling. TBID interacts with the hinge region through hydrophobic interactions between Val 213, Val 261, Phe 277, Leu 280, Met 331, Ile 345, and the tetrabromine moiety, while the symmetric nitrogen atom at position 3 interacts with the catalytic Lys 228, thus playing a crucial role in the binding architecture.

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