CAS NO: | 1219728-20-7 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
25mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
生物活性 |
SR7826 is a class of bis-aryl urea derived potent, selective and orally activeLIM kinase (LIMK)inhibitor with anIC50of 43 nM forLIMK1. SR7826 is >100-fold more selective forLIMK1thanROCKandJNKkinases[1]. |
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IC50& Target |
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体外研究 (In Vitro) |
In the profiling against a panel of 61 kinases, SR7826 (compound 18b) at 1 μM inhibits only Limk1 and STK16 with ≥80% inhibition. SR7826 is highly efficient in inhibiting cell-invasion/migration in PC-3 cells. SR7826 (compound 18b) inhibits cofilin phosphorylation in A7r5 (IC50= 470 nM) and PC-3 cells (IC50< 1 μM)[1].
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体内研究 (In Vivo) |
SR7826 (10 mg/kg; oral gavage; once daily; for 11 days; hAPPJ20 mice) treatment significantly reduces the phosphorylation of cofilin at Ser3. SR7826 also increases both apical and basal thin spine density significantly in hAPPJ20 mice over mock-treated animals[2].
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分子量 |
387.43 |
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性状 |
Solid |
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Formula |
C22H21N5O2 |
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CAS 号 |
1219728-20-7 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
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溶解性数据 |
In Vitro:
DMSO : 100 mg/mL(258.11 mM;Need ultrasonic)
配制储备液
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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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