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Merck
所有图片(1)

文件

688001

Sigma-Aldrich

Y-27632

≥95% (HPLC), liquid, Rho kinase inhibitor, Calbiochem®

别名:

InSolution Y-27632, Rho激酶抑制剂VI

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About This Item

经验公式(希尔记法):
C14H21N3O · 2HCl · xH2O
分子量:
320.26 (anhydrous basis)
分類程式碼代碼:
12352200
NACRES:
NA.77

product name

Y-27632, InSolution, ≥95%, reversible, inhibitor of Rho kinases

品質等級

化驗

≥95% (HPLC)

形狀

liquid

製造商/商標名

Calbiochem®

儲存條件

OK to freeze
protect from light

運輸包裝

wet ice

儲存溫度

−20°C

一般說明

Rho相关蛋白激酶的一种高效、细胞可渗透性、选择性抑制剂(针对p160ROCK(ROCK-I)的Ki= 140 nM)。还可几乎同等高效的抑制ROCK-II。抑制是通过与ATP竞争结合催化亚基而实现的。比p160ROCKε有10至50倍更低的PKC亲和力。即使在高浓度(~100 M)下也不影响p21激活蛋白激酶(PAK)的活性。还可作为肌球蛋白磷酸化和平滑肌收缩的激动剂诱导的Ca2+敏化的一种有效抑制剂(在主动脉环上针对苯肾上腺素诱导的收缩IC50 = 700 nM)。
可提供5 mM (500 µg/296 µl)的Y-27963(目录号 688000)的水溶液。Rho相关蛋白激酶的一种高效、细胞可渗透性、选择性抑制剂(针对p160ROCK(ROCK-I)的Ki= 140 nM)。还可几乎同等高效的抑制ROCK-II。抑制是通过与ATP竞争结合催化亚基而实现的。比p160ROCKε有10至50倍更低的PKC亲和力。即使在高浓度(~100 M)下也不影响p21激活蛋白激酶(PAK)的活性。还可作为肌球蛋白磷酸化和平滑肌收缩的激动剂诱导的Ca2+敏化的一种有效抑制剂(在主动脉环上针对苯肾上腺素诱导的收缩IC50 = 700 nM)。

生化/生理作用

主要靶标
p160ROCK
产物与ATP竞争。
可逆:否
细胞渗透性:是
靶标IC50:针对苯肾上腺素诱导的主动脉条收缩为700 nM
靶标Ki:对于p160ROCK (ROCK-I)为140 nM

包裝

用惰性气体包装

警告

毒性:有害(C)

外觀

5 mM (500 µg/296 µl)Y-27632(目录号688000)的H₂O溶液。

重構

初次融化后,等分并冷冻(-20°C)。

其他說明

Chitaley, K., et al. 2001.Nat. Med.7, 119.
Davies, S.P., et al. 2000.Biochem.J. 351, 95.
Narumiya, S., et al. 2000.Methods Enzymol.325, 273.
Hirose, M., et al. 1999.J. Cell Biol.141, 1625.
Maekawa, M., et al. 1999.Science285, 895.
Uehata, M., et al. 1997.Nature389, 990.

法律資訊

在PCT Application W098/06,433A1的许可和三菱制药田边分公司的许可下进行销售。
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

儲存類別代碼

12 - Non Combustible Liquids

水污染物質分類(WGK)

WGK 2

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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