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906050

Pomalidomide-C6-PEG1-C3-PEG1-butyl iodide

≥95%

Synonym(s):

Crosslinker−E3 Ligase ligand conjugate, Pomalidomide-6-5-6-I, N-(2-(2,6-Dioxopiperidin-3-yl)-1,3-dioxoisoindolin-4-yl)-6-((5-((6-iodohexyl)oxy)pentyl)oxy)hexanamide, Protein degrader building block for PROTAC® research, Template for synthesis of targeted protein degrader

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50 mg
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$582.00
$611.00

About This Item

Empirical Formula (Hill Notation):
C30H42IN3O7
CAS Number:
Molecular Weight:
683.57
MDL number:
UNSPSC Code:
12352101
NACRES:
NA.22

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ligand

pomalidomide

assay

≥95%

form

powder or crystals

reaction suitability

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

technique(s)

targeted protein degradation: suitable

functional group

alkyl halide

storage temp.

2-8°C

SMILES string

ICCCCCCOCCCCCOCCCCCC(NC1=CC=CC2=C1C(N(C3CCC(NC3=O)=O)C2=O)=O)=O

InChI key

ABEUETLCTXKUSX-UHFFFAOYSA-N

Application

Protein degrader builiding block Pomalidomide-C6-PEG1-C3-PEG1-Butyl Iodide enables the synthesis of molecules for targeted protein degradation and PROTAC (proteolysis-targeting chimeras) technology. This conjugate contains a Cereblon (CRBN)-recruiting ligand, a linker with both hydrophobic and hydrophilic moieties, and a pendant iodoalkane for reactivity with a nucleophilic group on a 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 pendant iodo group, 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

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This Item
904708904880904724
description

≥95%

description

≥95%

description

≥95%

description

≥95%

assay

≥95%

assay

≥95%

assay

≥95%

assay

≥95%

functional group

alkyl halide

functional group

alkyl halide

functional group

azide

functional group

alkyl halide

reaction suitability

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

reaction suitability

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

reaction suitability

reagent type: ligand-linker conjugate, reaction type: click chemistry

reaction suitability

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

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

form

powder or crystals

form

powder or crystals

form

powder or crystals

form

powder or crystals

ligand

pomalidomide

ligand

pomalidomide

ligand

pomalidomide

ligand

pomalidomide


Storage Class

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable



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