CAS NO: | 1783816-74-9 |
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 |
500mg | 电议 |
生物活性 |
NVS-PAK1-1 is a potent and selective allostericPAK1inhibitor with anIC50of 5 nM. |
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IC50& Target |
IC50: 5 nM (PAK1)[1] |
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体外研究 (In Vitro) |
NVS-PAK1-1 demonstrates high selectivity for inhibition of PAK1 over other PAK isoforms and the kinome in general. NVS-PAK1-1 has a biochemical PAK1 Kdof 7 nM and a PAK2 Kdof 400 nM. NVS-PAK1-1 shows excellent activity in biochemical assays and an exceptional selectivity profile against other known kinases. NVS-PAK1-1 at 6-20 μM inhibits the phosphorylation of the downstream substrate MEK1 Ser289. Consistent with the observation, NVS-PAK1-1 inhibits proliferation of Su86.86 cell line only above a concentration of 2 μM. In contrast, by applying a mixture of NVS-PAK1-1 and PAK2 shRNA, inhibition of downstream signaling and cell proliferation at a significantly lower 0.21 μM concentration are achieved[1].
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体内研究 (In Vivo) |
NVS-PAK1-1 shows a relatively poor stability in rat liver microsomes (RLM) and this would limit its application forin vivostudies (t1/2in RLM 3.5 min)[1].
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分子量 |
479.93 |
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性状 |
Solid |
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Formula |
C23H25ClF3N5O |
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CAS 号 |
1783816-74-9 |
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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 : ≥ 125 mg/mL(260.45 mM) *"≥" means soluble, but saturation unknown.
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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