Basic information Safety Supplier Related

Pomalidomide-NH-PEG3-azide

Basic information Safety Supplier Related

Pomalidomide-NH-PEG3-azide Basic information

Product Name:
Pomalidomide-NH-PEG3-azide
Synonyms:
  • Pomalidomide-NH-PEG3-azide
  • IUN-36463
  • 4-((2-(2-(2-(2-azidoethoxy)ethoxy)ethoxy)ethyl)amino)-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione
  • Pomalidomide 4'-PEG3-azide
  • 1H-Isoindole-1,3(2H)-dione, 4-[[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethyl]amino]-2-(2,6-dioxo-3-piperidinyl)-
  • 4-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethylamino]-2-(2,6-dioxopiperidin-3-yl)isoindole-1,3-dione
CAS:
2271036-46-3
MF:
C21H26N6O7
MW:
474.47
Mol File:
2271036-46-3.mol
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Pomalidomide-NH-PEG3-azide Chemical Properties

form 
Solid
color 
Light yellow to yellow
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Safety Information

HS Code 
2933998090
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Pomalidomide-NH-PEG3-azide Usage And Synthesis

Uses

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[1]. 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.

IC 50

Cereblon

storage

Store at -20°C

References

[1] Shuai Wang, et al. Uncoupling of PARP1 trapping and inhibition using selective PARP1 degradation. Nat Chem Biol. 2019 Dec;15(12):1223-1231. DOI:10.1038/s41589-019-0379-2

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