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LY 294002-CAS 154447-36-6-Calbiochem

品牌
Sigma-Aldrich
CAS
154447-36-6
货号
440202
规格纯度
LY294002, CAS 154447-36-6, is a cell-permeable, potent, reversible, and specific inhibitor of PI 3-kinase ((IC50= 1.4 μM). Acts on the ATP-binding site.
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2741.8 *本价格含增值税费
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半岛bd体育手机客户端 名称:
154447-36-6
LY 294002-CAS 154447-36-6-Calbiochem
2-(4-Morpholinyl)-8-phenyl-4H-1-benzopyran-4-one, BRD2 Inhibitor IV, BRD3 Inhibitor III, BRD4 Inhibitor IV
半岛bd体育手机客户端 介绍:

半岛bd体育手机客户端 说明

一般描述

A cell-permeable, potent, reversible and specific phosphatidylinositol 3-kinase inhibitor (IC50= 1.4 ?M) that acts on the ATP-binding site of the enzyme. Also inhibits nonhomologous DNA end-joining (NHEJ) activity of the 460 kDa phosphatidylinositol 3-like kinase DNA-PKcs, which is the catalytic subunit of DNA-activated protein kinase. Does not affect the activities of EGF receptor kinase, MAP kinase, PKC, Pl 4-kinase, S6 kinase, and c-Src even at 50 ?M. Promotes the nuclear accumulation of active GSK-3b. Reported to suppress the proliferation of murine embryonic stem cells. Blocks the proliferation of cultured rabbit aortic smooth muscle cells without inducing apoptosis. Shown to bind to the same site as I-BET (Cat. No. 40101050~ 10 ?M). A 10 mM (1 mg/325 ?l) solution of LY 294002 (Cat. No. 440204) in DMSO is also available.
A cell-permeable, potent, reversible, and specific phosphatidylinositol 3-kinase (PI 3-kinase) inhibitor that acts on the ATP-binding site of the enzyme (IC50= 1.4 ?M). Also inhibits nonhomologous DNA end-joining (NHED) in the 460 kDa phosphatidylinositol 3-like kinase DNA-PKcs, which is the catalytic subunit of DNA-activated protein kinase. Does not affect the activity of EGF receptor kinase, MAP kinase, PKC, PI 4-kinase, S6 kinase, and c-src at 50 ?M. Promotes the nuclear accumulation of active GSK-3b. Reported to suppress the proliferation of murine embryonic stem cells. Blocks the proliferation of cultured rabbit aortic smooth muscle cells without inducing apoptosis. Reported to inhibit histamine secretion in RBL-2H3 cells (IC50= 5 ?M).

包装

5, 10, 25 mg in Plastic ampoule

生化/生理作用

Cell permeable: yes
Target IC50: 1.4 ?M against phosphatidylinositol 3-kinase
Primary Target
Phosphatidylinositol 3-kinase
Product competes with ATP.
Reversible: yes

警告

Toxicity: Standard Handling (A)

制备说明

Slight warming may be required to achieve complete solubilization.

重悬

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 6 months at -20°C.

其他说明

Dittman, A., et al. 2013.ACS Chem. Biol.9,495.
Bechard, M., and Dalton. S. 2009.Mol. Cell. Biol.29,2092.
Lianguzova, M.S. et al. 2007.Cell Biol. Int.31,330.
Baumann, P., and West, S.C. 1998.Proc. Natl. Acad. Sci. USA95,14066.
Cardone, M.H., et al. 1998.Science282,1318.
Vlahos, C.J., et al. 1995.J. Immunol.154,2413.
Yano, H., et al. 1995.Biochem. J.312,145.
Vlahos, C.J., et al. 1994.J. Biol. Chem.269,5241.



Selected Citations
Lee, J., et al. 2009. Cell Stem Cell 5,76.


法律信息

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

基本信息

经验(实验)分子式 C19H17NO3
分子量 307.34

半岛bd体育手机客户端 性质

质量水平 100
测定 ≥98% (HPLC)
形式 solid
manufacturer/tradename Calbiochem?
储存条件 OK to freeze
protect from light
颜色 off-white
溶解性 DMSO: 20 mg/mL
ethanol: soluble
运输 ambient
储存温度 ?20℃
InChI 1S/C19H17NO3/c21-17-13-18(20-9-11-22-12-10-20)23-19-15(7-4-8-16(17)19)14-5-2-1-3-6-14/h1-8,13H,9-12H2
InChI key CZQHHVNHHHRRDU-UHFFFAOYSA-N

安全信息

储存分类代码 11 - Combustible Solids
WGK WGK 2
闪点(F) 487.4 °F
闪点(C) 253.0 ℃

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