CAS NO: | 677331-12-3 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
生物活性 | iCRT 14 is a novel potent inhibitor ofβ-catenin-responsive transcription (CRT), withIC50of 40.3 nM againstWntresponsive STF16 luciferase. | ||||||||||||||||
IC50& Target | IC50: 40.3 nM (Wnt responsive STF16 luciferase)[1] | ||||||||||||||||
体外研究 (In Vitro) | iCRT14 can interfere with TCF binding to DNA in addition to its ability to influence TCF-β-cat interaction[1]. iCRT14 (10, 25, 50 μM) effectively inhibits cell proliferation in BT-549 cells in a dose- and time-dependent manner, but still less potent than iCRT3[2]. | ||||||||||||||||
体内研究 (In Vivo) | iCRT14 (50 mg/kg, i.p.) markedly decreases CycD1, proliferation of the tumors in HCT116 xenografts[1]. | ||||||||||||||||
分子量 | 375.44 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C21H17N3O2S | ||||||||||||||||
CAS 号 | 677331-12-3 | ||||||||||||||||
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 : ≥ 29 mg/mL(77.24 mM) *"≥" means soluble, but saturation unknown. 配制储备液
* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo: 请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用;
以下溶剂前显示的百
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