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Merck
CN

916587

Sigma-Aldrich

3-(1-(tert-Butoxycarbonyl)piperidin-4-yl)benzoic acid

≥95%

别名:

Semi-flexible linker for PROTAC® development

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About This Item

经验公式(希尔记法):
C17H23NO4
分子量:
305.37
MDL编号:
UNSPSC代码:
12352106

质量水平

方案

≥95%

表单

powder

反应适用性

reagent type: linker

官能团

Boc
carboxylic acid

储存温度

2-8°C

SMILES字符串

O=C(OC(C)(C)C)N1CCC(C2=CC(C(O)=O)=CC=C2)CC1

InChI

1S/C17H23NO4/c1-17(2,3)22-16(21)18-9-7-12(8-10-18)13-5-4-6-14(11-13)15(19)20/h4-6,11-12H,7-10H2,1-3H3,(H,19,20)

InChI key

PDPYHAXCPUSEMT-UHFFFAOYSA-N

应用

3-(1-(tert-Butoxycarbonyl)piperidin-4-yl)benzoic acid is a 4-aryl piperidine useful as a semi-flexible linker in PROTAC development for targeted protein degradation. Incorporation of rigidity into the linker region of bifunctional protein degraders may impact the 3D orientation of the degrader and thus ternary complex formation as well as optimization of drug-like properties.

法律信息

PROTAC is a registered trademark of Arvinas Operations, Inc., and is used under license

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Warning

危险分类

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

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历史批次信息供参考:

分析证书(COA)

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Haifeng Tang et al.
Bioorganic & medicinal chemistry letters, 20(20), 6088-6092 (2010-09-14)
A new series of thiazole-substituted 1,1,1,3,3,3-hexafluoro-2-propanols were prepared and evaluated as malonyl-CoA decarboxylase (MCD) inhibitors. Key analogs caused dose-dependent decreases in food intake and body weight in obese mice. Acute treatment with these compounds also led to a drop in

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