SIRT2 Inhibitor, AGK2,5MG,566324-5MGCN,Sigma

销售价: ¥ 1892.70 / 件
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订货号 : 0BV9708
品牌型号 : Sigma 566324-5MGCN
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 cell-permeable quinoline compound that targets the nicotinamide-binding site and acts as a reversible sirtuin 2- (SIRT2) selective inhibitor (IC50 = 3.5 µM) with little activity against SIRT1/3 (IC50 >50 µM). Prevents cellular α-tubulin deacetylation in HeLa cells in a dose-dependent manner and with little cytotoxic effect. Shown to rescue α-Synuclein-mediated toxicity both in primary rat embryo midbrain cultures in vitro and in a Drosophila PD model in vivo. The inactive isomer AGK7 (Cat. No. 566326) can be used as a negative control.


Packaging

Packaged under inert gas


Preparation Note

Slight warming may be required for complete solubilization.


Other Notes

Outerio, T.F., et al. 2007. Science317, 516.


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
color yellow
solubilityDMSO: 2.5 mg/mL
shipped inambient
storage temp.2-8°C
SMILES stringClc1c(cc(cc1)Cl)c2[o]c(cc2)\C=C(\C(=O)Nc3c4c(nccc4)ccc3)/C#N
InChI1S/C23H13Cl2N3O2/c24-15-6-8-19(25)18(12-15)22-9-7-16(30-22)11-14(13-26)23(29)28-21-5-1-4-20-17(21)3-2-10-27-20/h1-12H,(H,28,29)/b14-11+
InChI keySVENPFFEMUOOGK-SDNWHVSQSA-N
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