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Merck
CN

919489

Sigma-Aldrich

CCW16-C6-PEG3-butyl-BocNH

别名:

tert-butyl (6-(2-(2-((6-(4-(4-(N-Benzyl-2-chloroacetamido)phenoxy)phenoxy)hexyl)oxy)ethoxy)ethoxy)hexyl)carbamate, Crosslinker-E3 Ligase ligand conjugate, Protein degrader building block for PROTAC® research, RNF4-targeting building block, Template for synthesis of targeted protein degrader

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About This Item

经验公式(希尔记法):
C42H59ClN2O8
分子量:
755.38
MDL编号:
UNSPSC代码:
12352200
NACRES:
NA.22

ligand

CCW16

质量水平

表单

viscous liquid

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=C(CCl)N(CC1=CC=CC=C1)C2=CC=C(C=C2)OC3=CC=C(OCCCCCCOCCOCCOCCCCCCNC(OC(C)(C)C)=O)C=C3

InChI

1S/C42H59ClN2O8/c1-42(2,3)53-41(47)44-25-11-4-5-12-26-48-29-31-50-32-30-49-27-13-6-7-14-28-51-37-21-23-39(24-22-37)52-38-19-17-36(18-20-38)45(40(46)33-43)34-35-15-9-8-10-16-35/h8-10,15-24H,4-7,11-14,25-34H2,1-3H3,(H,44,47)

InChI key

MBDBAPHHKCSIAT-UHFFFAOYSA-N

应用

Protein degrader building block CCW16-C6-PEG3-butyl-BocNH enables the synthesis of molecules for targeted protein degradation and PROTAC (proteolysis-targeting chimeras) technology. This conjugate contains a RING finger protein 4 (RNF4)-recruiting ligand, a linker with both hydrophobic and hydrophilic moieties, and a pendant amine for reactivity with a carboxylic acid on the target ligand. 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

储存分类代码

10 - Combustible liquids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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