MK2a Inhibitor,5MG,475863-5MGCN,Sigma

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订货号 0BV5996
品牌型号 Sigma 475863-5MGCN
货期 询货期
最小订货量 1件
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产品介绍 Product Description

General description

A non-ATP-competitive, reversible, selective inhibitor of p38α-mediated MK2a (mitogen-activated protein kinase-activated protein kinase 2a) phosphorylation (Kiapp = 330 nM). Does not inhibit p38α-mediated phosphorylation of the the other two known p38 substrates, MBP and ATF-2.
A reversible p-amidophenolic compound that selectively inhibits the phosphorylation of MK2a (mitogen-activated protein kinase-activated protein kinase 2a; Kiapp = 330 nM) by p38α in a non-ATP-competitive manner. Does not block the kinase activity of p38α towards the other two known p38 substrates, MBP and ATF-2.


Biochem/physiol Actions

Cell permeable: no
Kiapp = 330 nM against mitogen-activated protein kinase-activated protein kinase 2a (MK2a)
Primary Target
Mk2α
Product does not compete with ATP.
Reversible: yes


Packaging

Packaged under inert gas


Preparation Note

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.


Other Notes

Davidson, W., et al. 2004. Biochemistry43, 11658.
Lukas, S.M., et al. 2004. Biochemistry43, 9950.


Legal Information

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


Disclaimer

Toxicity: Standard Handling (A)


技术参数 Specifications
Quality Segment100
assay≥95% (HPLC)
formsolid
manufacturer/tradenameCalbiochem®
storage conditionOK to freeze,protect from light
colorpale yellow
solubilityDMSO: 5 mg/mL,ethanol: 5 mg/mL
shipped inambient
storage temp.2-8°C
SMILES stringFc1c(cccc1)c2ccc(cc2)CCCC(=O)Nc3ccc(cc3)O
InChI1S/C22H20FNO2/c23-21-6-2-1-5-20(21)17-10-8-16(9-11-17)4-3-7-22(26)24-18-12-14-19(25)15-13-18/h1-2,5-6,8-15,25H,3-4,7H2,(H,24,26)
InChI keyODYAQBDIXCVKAE-UHFFFAOYSA-N
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