
Pomalidomide 4-PEG3-azide
CAS No. 2271036-46-3
Pomalidomide 4-PEG3-azide( —— )
Catalog No. M35159 CAS No. 2271036-46-3
Pomalidomide 4'-PEG3-azide is a chemically synthesized E3 ligase ligand-linker conjugate that incorporates the cereblon ligand derived from Pomalidomide, along with a linker.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
5MG | 46 | Get Quote |
![]() ![]() |
10MG | 77 | Get Quote |
![]() ![]() |
25MG | 150 | Get Quote |
![]() ![]() |
50MG | 242 | Get Quote |
![]() ![]() |
100MG | 381 | Get Quote |
![]() ![]() |
500MG | 861 | Get Quote |
![]() ![]() |
1G | Get Quote | Get Quote |
![]() ![]() |
Biological Information
-
Product NamePomalidomide 4-PEG3-azide
-
NoteResearch use only, not for human use.
-
Brief DescriptionPomalidomide 4'-PEG3-azide is a chemically synthesized E3 ligase ligand-linker conjugate that incorporates the cereblon ligand derived from Pomalidomide, along with a linker.
-
DescriptionPomalidomide 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. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayOthers
-
TargetOther Targets
-
RecptorE3 Ligase Ligand-Linker Conjugate
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number2271036-46-3
-
Formula Weight474.47
-
Molecular FormulaC21H26N6O7
-
Purity>98% (HPLC)
-
Solubility——
-
SMILES[N-]=[N+]=NCCOCCOCCOCCNC1=CC=CC=2C(=O)N(C(=O)C12)C3C(=O)NC(=O)CC3
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Shuai Wang, et al. Uncoupling of PARP1 trapping and inhibition using selective PARP1 degradation. Nat Chem Biol. 2019 Dec;15(12):1223-1231.?
molnova catalog



related products
-
Bancroftinone
Bancroftinone is a natural product.
-
SARS-CoV-2-IN-38
SARS-CoV-2-IN-38 is an orally available SARS-CoV-2 inhibitor with potential antiviral activity for the study of SARS viral infections.
-
Vindoline
Vindoline is an indole alkaloid that exhibits antimitotic activity by inhibiting microtubule assembly.