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InSolution PD 98059 - CAS 167869-21-8 - Calbiochem

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InSolution PD 98059 - CAS 167869-21-8 - Calbiochem

产品详情

中文名称 InSolution PD 98059 - CAS 167869-21-8 - Calbiochem 别名
CasNo 167869-21-8 产品类别
产品编号513000
品牌Sigma
形式solid
警告Toxicity: Standard Handling (A)
测定≥98% (HPLC)
颜色pale yellow
运输ambient
分子量267.28
溶解性methanol: 0.7?mg/mL
DMSO: 20?mg/mL
储存温度?20°C
质量水平100
储存条件OK to freeze
protect from light
MDL编号MFCD00671789

别名

PD 98059 - CAS 167869-21-8 - Calbiochem,2ʹ-Amino-3ʹ-methoxyflavone, MEK Inhibitor V

一般描述

Selective, reversible, and cell-permeable inhibitor of MAP kinase kinase (MEK) that acts by inhibiting the activation of MAP kinase and subsequent phosphorylation of MAP kinase substrates (noncompetitive with respect to ATP). Pretreatment of PC-12 cells with PD 98059 completely blocks the 4-fold increase of MAP kinase activity produced by nerve growth factor (NGF; IC50 = 2 μM); however, it has no effect on NGF-dependent tyrosine phosphorylation of the pp140trk receptor or its substrate Shc and does not block NGF-dependent activation of PI 3-kinase. Inhibits cell growth and reverses the phenotype of ras-transformed BALB 3T3 mouse fibroblasts and rat kidney cells. Selective, reversible, and cell-permeable inhibitor of MAP kinase kinase (MEK) that acts by inhibiting the activation of MAP kinase and subsequent phosphorylation of MAP kinase substrates. Pretreatment of PC-12 cells with PD 98059 completely blocks the 4-fold increase in MAP kinase activity produced by nerve growth factor (NGF; IC50 = 2 μM); however, it has no effect on NGF-dependent tyrosine phosphorylation of the p140trk receptor or its substrate Shc and does not block NGF-dependent activation of PI 3-kinase. Blocks LPS-induced activation of TNF-α gene expression. Inhibits cell growth and reverses the phenotype of ras-transformed BALB3T3 mouse fibroblasts and rat kidney cells. A 5 mg/ml solution of PD 98059 (Cat. No. 513001) in anhydrous DMSO is also available.

生化/生理作用

Cell permeable: yes Primary Target
MAP kinase kinase (MEK) Product does not compete with ATP. Reversible: yes Target IC50: 2 μM against NGF-induced increase in MAP kinase activity

重悬

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 4 months at -20°C.

其他说明

Means, T.K., et al. 2000. J. Leukoc. Biol. 67, 885.
Kültz, D., et al. 1998. J. Biol. Chem. 273, 13645.
Dudley, D.T., et al. 1995. Proc. Natl. Acad. Sci. USA92, 7686.
Langlois, W.J., et al. 1995. J. Biol. Chem. 270, 25320.
Pang, L., et al. 1995. J. Biol. Chem.270, 13585.
Waters, S.B., et al. 1995. J. Biol. Chem.270, 20883.

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