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Merck
CN

919969

Sigma-Aldrich

C5 Lenalidomide-PEG2-Butyl NH2 hydrochloride

≥95%

别名:

2-(2-((6-Aminohexyl)oxy)ethoxy)-N-(2-(2,6-dioxopiperidin-3-yl)-1-oxoisoindolin-5-yl)acetamide hydrochloride, C5 Lenalidomide conjugate, Crosslinker−E3 Ligase ligand conjugate, Protein degrader building block for PROTAC® research, Template for synthesis of targeted protein degrader

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About This Item

经验公式(希尔记法):
C23H32N4O6 · xHCl
分子量:
460.52 (free base basis)
MDL编号:
UNSPSC代码:
12352101
NACRES:
NA.22

ligand

C5 Lenalidomide

质量水平

方案

≥95%

表单

powder or crystals

反应适用性

reactivity: carboxyl reactive
reagent type: ligand-linker conjugate

官能团

amine

储存温度

2-8°C

SMILES字符串

O=C1N(C2CCC(NC2=O)=O)CC3=CC(NC(COCCOCCCCCCN)=O)=CC=C31.Cl

InChI

1S/C23H32N4O6.ClH/c24-9-3-1-2-4-10-32-11-12-33-15-21(29)25-17-5-6-18-16(13-17)14-27(23(18)31)19-7-8-20(28)26-22(19)30;/h5-6,13,19H,1-4,7-12,14-15,24H2,(H,25,29)(H,26,28,30);1H

InChI key

HDOCYCRRBNJXSG-UHFFFAOYSA-N

应用

Protein degrader building block C5 Lenalidomide-PEG2-Butyl NH2 hydrochloride enables the synthesis of molecules for targeted protein degradation and PROTAC (proteolysis-targeting chimeras) technology. This conjugate contains a Cereblon (CRBN)-recruiting ligand with alternative exit vector, a linker with both hydrophobic and hydrophilic moieties, and a pendant amine for reactivity with an acid on the target warhead. Because even slight alterations in ligands and crosslinkers can affect ternary complex formation between the target, E3 ligase, and PROTAC, many analogs are prepared to screen for optimal target degradation. When used with other protein degrader building blocks with a terminal amine, parallel synthesis can be used to more quickly generate PROTAC libraries that feature variation in crosslinker length, composition, and E3 ligase ligand.

法律信息

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

相关产品

产品编号
说明
价格

储存分类代码

11 - Combustible Solids

WGK

WGK 3

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Protein Degrader Building Blocks are a collection of crosslinker-E3 ligand conjugates with a pendant functional group for covalent linkage to a target ligand.

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