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Merck
CN

919969

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

SMILES string

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

ligand

C5 Lenalidomide

assay

≥95%

form

powder or crystals

reaction suitability

reactivity: carboxyl reactive, reagent type: ligand-linker conjugate

functional group

amine

storage temp.

2-8°C

Quality Level

Application

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.

Legal Information

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

存储类别

11 - Combustible Solids

wgk

WGK 3

法规信息

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商品

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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