CAS NO: | 78957-85-4 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | A-3 hydrochloride is a potent, cell-permeable, reversible, ATP-competitive non-selective antagonist of variouskinases. It againstPKA(Ki=4.3 μM),casein kinaseII (Ki=5.1 μM) andmyosinlight chain kinase (MLCK) (Ki=7.4 μM). A-3 hydrochloride also inhibitsPKCandcasein kinaseI withKivalues of 47 μM and 80 μM, respectively[1]. | ||||||||||||||||
IC50& Target[1] |
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体外研究 (In Vitro) | A-3 hydrochloride inhibits MLC-kinase competitively with respect to ATP and that the Kivalue is 7.4 μM. A-3 is also a competitive inhibitor of cAMP-dependent protein kinase, cGMP-dependent protein kinase, protein kinase C, casein kinase I, and casein kinase II, with respect to ATP, exhibits Kivalues of 4.3 μM, 3.8 μM, 47 μM, 80 μM, and 5.1 μM, respectively[1]. | ||||||||||||||||
分子量 | 321.22 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C12H14Cl2N2O2S | ||||||||||||||||
CAS 号 | 78957-85-4 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 | 4°C, sealed storage, away from moisture *In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture) | ||||||||||||||||
溶解性数据 | In Vitro: DMSO : 125 mg/mL(389.14 mM;Need ultrasonic) H2O : 50 mg/mL(155.66 mM;Need ultrasonic) 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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