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Supplier NameMedChemExpress (MCE)
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Product NamePomalidomide 4'-PEG3-azide
SynonymsIUN-36463;Pomalidomide 4'-PEG3-azide;Pomalidomide-NH-PEG3-azide;4-((2-(2-(2-(2-azidoethoxy)ethoxy)ethoxy)ethyl)amino)-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione
CAS2271036-46-3
EINECS
Chemical FormulaC21H26N6O7
Molecular Weight474.47
inchi
Package1 mg;5 mg;10 mg;25 mg;50 mg;100 mg
PriceEmail to quote
DescriptionsPomalidomide 4'-PEG3-azide

Pomalidomide 4'-PEG3-azide

MedChemExpress (MCE)

HY-130652

2271036-46-3

96.06%

Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month

Room temperature in continental US

Descriptions

Pomalidomide 4'-PEG3-azide

Pomalidomide 4'-PEG3-azide

MedChemExpress (MCE)

HY-130652

2271036-46-3

96.06%

Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month

Room temperature in continental US
may vary elsewhere.

Pomalidomide 4'-PEG3-azide is a synthesized E3 ligase ligand-linker conjugate that incorporates the Pomalidomide-based cereblon ligand and a linker. Pomalidomide 4'-PEG3-azide can be used for the synthesis of iRucaparib-TP3 (Compound 3). iRucaparib-TP3 is a highly efficient PARP1?degrader based on Rucaparib by using the PROTAC approach. Pomalidomide 4'-PEG3-azide is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.

Cereblon

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[1]. Shuai Wang, et al. Uncoupling of PARP1 trapping and inhibition using selective PARP1 degradation. Nat Chem Biol. 2019 Dec
15(12):1223-1231.
[Content Brief]

Supplier Websitehttps://www.medchemexpress.com/pomalidomide-4-peg3-azide.html
Last Update2025-05-21 16:50:25
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