TBOPP is a selective DOCK1 inhibitor with IC50 value of 8.4μM. It dampened DOCK1-mediated invasion, macropinocytosis, and survival under the condition of glutamine deprivation. TBOPP treatment suppressed cancer metastasis and growth in vivo in mice.
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描述 | The dedicator of cytokinesis (DOCK) family is one of the two members of the RAC guanine nucleotide exchange factor (GEF) family. DOCK1 regulates phagocytosis, myoblastic fusion, cell migration and circular dorsal fold formation[2]. TBOPP is a selective inhibitor of Dock1 which inhibits Dock1-mediated Rac activation with an IC50 of 8.4 μM and binds DOCK1 DHR-2 domain with a KD of 7.1 mM[3]. TBOPP decreased RCC (renal cell carcinoma) cell viability from 10 µM in a concentration-dependent manner and significantly decreased cell proliferation at 10 and 40 µM. TBOPP (10 µM) inhibited RCC cell cisplatin resistance in RCC cells[2]. TBOPP treatment for 48 hr induced a significantly high level of cell death in JEG-3 cells[4]. |
作用机制 | TBOPP binds to the DHR-2 domain of DOCK1[2]. |
计算器 | ||||
存储液制备 | 1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
2.04mL 0.41mL 0.20mL |
10.19mL 2.04mL 1.02mL |
20.39mL 4.08mL 2.04mL |
CAS号 | 1996629-79-8 |
分子式 | C24H21F3N2O4S |
分子量 | 490.495 |
别名 | |
运输 | 蓝冰 |
存储条件 |
液体 -20°C:3-6个月-80°C:12个月 粉末 Keep in dark place,Inert atmosphere,Room temperature |
溶解度 |
DMSO: 105 mg/mL(214.07 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO |
动物实验配方 |