CAS NO: | 1380672-07-0 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
2mg | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | G007-LK is a potent and selective inhibitor ofTNKS1andTNKS2, withIC50s of 46 nM and 25 nM, respectively. | ||||||||||||||||
IC50& Target[1] |
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体外研究 (In Vitro) | G007-LK is a potent inhibitor of TNKS1 and TNKS2, with IC50s of 46 nM and 25 nM, respectively, and a cellular IC50of 50 nM. G007-LK shows no inhibition of PARP1 at doses up to 20 μM, and has a high CYP3A4 inhibition IC50value (>25 μM)[1]. G007-LK (0-20 μM) dose-dependently inhibits hepatocellular carcinoma (HCC) cell growth. G007-LK also downregulates the levels of YAP by upregulating AMOTL1 and AMOTL2 in HCC cell lines. In addition, G007-LK (0-20 μM) synergizes with MEK and AKT inhibitors to suppress HCC cell proliferation[3]. | ||||||||||||||||
体内研究 (In Vivo) | G007-LK displays great pharmacokinetic profile in ICR mice[1]. G007-LK (100 mg/kg chow, p.o.) significantly reduces lineage tracing from LGR5+intestinal stem cells in mice. G007-LK (100 mg/kg chow, p.o.) specifically targets LGR5+WNT-dependent intestinal stem cells in Lgr5-EGFP-CreERT2;R26R-tdTomato mice. G007-LK (10, 50 mg/kg, p.o.) also suppressses canonical WNT signalling. Furthermore, G007-LK (100, 1000 mg/kg chow, p.o) shows no effect on the alteration of duodenal morphology[2]. | ||||||||||||||||
分子量 | 529.96 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C25H16ClN7O3S | ||||||||||||||||
CAS 号 | 1380672-07-0 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : ≥ 30 mg/mL(56.61 mM) *"≥" means soluble, but saturation unknown. 配制储备液
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以下溶剂前显示的百
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