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Merck
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文件

203390

Sigma-Aldrich

(±)-Blebbistatin

≥97% (HPLC), solid, Myosin II inhibitor, Calbiochem®

别名:

(±)-博司他汀

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About This Item

经验公式(希尔记法):
C18H16N2O2
分子量:
292.33
分類程式碼代碼:
12352200
NACRES:
NA.77

product name

(±)-Blebbistatin, (±)-Blebbistatin, CAS 674289-55-5, is a cell-permeable, selective, and reversible inhibitor of nonmuscle myosin II. Blocks cell blebbing and disrupts cell migration & cytoKinesis in vertebrate cells.

品質等級

化驗

≥97% (HPLC)

形狀

solid

製造商/商標名

Calbiochem®

儲存條件

OK to freeze
protect from light

顏色

yellow

溶解度

methanol: 1.5 mg/mL
100% DMSO: 100 mg/mL
90% DMSO: 75 mg/mL

運輸包裝

wet ice

儲存溫度

−20°C

InChI

1S/C18H16N2O2/c1-12-7-8-15-14(11-12)16(21)18(22)9-10-20(17(18)19-15)13-5-3-2-4-6-13/h2-8,11,22H,9-10H2,1H3

InChI 密鑰

LZAXPYOBKSJSEX-UHFFFAOYSA-N

一般說明

一种可渗透细胞的化合物,作为非肌肉肌球蛋白Ⅱ的选择性、强效和可逆抑制剂。抑制人血小板(≤100 µM)的ATP酶和滑动运动,而不影响肌球蛋白轻链激酶(MLCK)的活性。已经显示出可以阻止细胞起泡并迅速破坏脊椎动物细胞中的定向细胞迁移和胞质分裂。不会破坏有丝分裂或影响收缩环的组装。
一种可渗透细胞的化合物,作为非肌肉肌球蛋白Ⅱ的选择性、强效和可逆抑制剂。抑制人血小板(≤100 µM)的ATP酶和滑动运动,而不影响肌球蛋白轻链激酶(MLCK)的活性。已经显示出可以阻止细胞起泡并迅速破坏脊椎动物细胞中的定向细胞迁移和胞质分裂。不会破坏有丝分裂或影响收缩环的组装。也可使用50 mM(5 mg/342 µl)(±)-Blebbistatin在90% DMSO的溶液(目录号203389)。

生化/生理作用

主要靶标
ATPase
产物不与ATP竞争。
可逆性:是
细胞可渗透性:是
靶标IC50:<100 µM 抑制人血小板的ATP酶和滑动运动

包裝

用惰性气体包装

重構

在90% DMSO中复溶后,等分并冷冻保存(-20°C)。90% DMSO中的储备液可在-20°C下稳定保存1个月。100%DMSO中的储备溶液不稳定;临用前复溶。

其他說明

Shu, S., et al. 2005.Proc.Natl.Acad.Sci. USA102, 1472.
Kovacs, M., et al. 2004.J. Biol. Chem.279, 35557.
Straight, A.F., et al. 2003.Science299, 1743.
Cheung, A., et al. 2001.Mol.Biol. Cell Suppl.12, 271a.

法律資訊

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 2

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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