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EZ-482 Sale

目录号 : GC60158

EZ-482 是载脂蛋白 (apoE) 的新型配体,与 apoE 的 C-末端域上的位点结合,对于 apoE3 和 apoE4 的 Kd 值为 5-10 μM。EZ-482 通过独特的 N 末端变构作用与 apoE4 结合。EZ482 有用于阿尔茨海默氏病的潜力。

EZ-482 Chemical Structure

Cas No.:1016456-76-0

规格 价格 库存 购买数量
5mg
¥1,620.00
现货
10mg
¥2,700.00
现货
25mg
¥5,400.00
现货
50mg
¥8,550.00
现货
100mg
¥14,400.00
现货

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Sample solution is provided at 25 µL, 10mM.

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产品描述

EZ-482, a novel ligand of apolipoprotein (apoE), binds to sites on apoE in the C-terminal domain with Kds of 5-10 μM for apoE3 and apoE4. EZ-482 binds to apoE4 by a unique N-terminal allosteric effect. EZ482 has the potential for Alzheimer's diseas[1].

EZ-482 binds to sites on apoE in the C-terminal domain encompassing residues 229-243 and 258-265[1]. EZ-482 (0.5, 1, 5, 10 μM; 1 hour) blocks heparin binding in a concentration-dependent manner[1].

[1]. Tridib Mondal, et al. ApoE: In Vitro Studies of a Small Molecule Effector. Biochemistry. 2016 May 10;55(18):2613-21.

Chemical Properties

Cas No. 1016456-76-0 SDF
Canonical SMILES O=C(NC1=CC(S(=O)(NC2=CC=CC(Cl)=C2)=O)=CC=C1O)CC3=NN(C)C(C4=C3C=CC=C4)=O
分子式 C23H19ClN4O5S 分子量 498.94
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1 mM 2.0042 mL 10.0212 mL 20.0425 mL
5 mM 0.4008 mL 2.0042 mL 4.0085 mL
10 mM 0.2004 mL 1.0021 mL 2.0042 mL
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Research Update

ApoE: In Vitro Studies of a Small Molecule Effector

Biochemistry 2016 May 10;55(18):2613-21.PMID:27065061DOI:PMC4976638

Apolipoprotein E4 (apoE4), one of three isoforms of apoE, is the major risk factor for developing late onset Alzheimer's disease. The only differences among these isoforms (apoE2, apoE3, and apoE4) are single amino acid changes. Yet these proteins are functionally very different. One approach to ameliorating the effect of apoE4 with respect to Alzheimer's disease would be to find small molecular weight compounds that affect the behavior of apoE4. Few studies of this approach have been carried out in part because there was no complete structure of any full-length apoE isoform until 2011. Here, we focus on one small molecular weight compound, EZ-482, and explore the effects of its binding to apoE. Using hydrogen-deuterium exchange, we determined that EZ-482 binds to the C-terminal domains of both apoE3 and apoE4. The binding to apoE4, however, is accompanied by a unique N-terminal allosteric effect. Using fluorescence methods, we determined an apparent dissociation constant of approximately 8 μM. Although EZ-482 binds to the C-terminal domain, it blocks heparin binding to the N-terminal domain. The residues of apoE that bind heparin are the same as those involved in apoE binding to LDL and LRP-1 receptors. The methods and the data presented here may serve as a template for future studies using small molecular weight compounds to modulate the behavior of apoE.