| Identification | Back Directory | [Name]
Boc-aminooxy-PEG1-Propargyl | [CAS]
1895922-72-1 | [Synonyms]
Boc-aminooxy-PEG1-Propargyl
t-Boc-aminooxy-PEG1-propargyl
Carbamic acid, N-[2-(2-propyn-1-yloxy)ethoxy]-, 1,1-dimethylethyl ester | [Molecular Formula]
C10H17NO4 | [MDL Number]
MFCD29764325 | [MOL File]
1895922-72-1.mol | [Molecular Weight]
215.25 |
| Hazard Information | Back Directory | [Description]
t-Boc-aminooxy-PEG1-propargyl is a click chemistry PEG linker with a t-Boc-aminooxy group. The propargyl group can react with azide-bearing compounds or biomolecules via copper catalyzed azide-alkyne Click Chemistry to yield a stable triazole linkage. The t-Boc aminooxy group can be deprotected under mild acidic conditions and then can react with an aldehyde or ketone group to form a stable oxime linkage. The hydrophilic PEG spacer increases solubility in aqueous media. | [Uses]
Boc-aminooxy-PEG1-propargyl is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. Boc-aminooxy-PEG1-propargyl is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. | [IC 50]
PEGs; Alkyl/ether | [References]
[1] Zhao B, et al. Protein Engineering in the Ubiquitin System: Tools for Discovery and Beyond. Pharmacol Rev. 2020 Apr;72(2):380-413. DOI:10.1124/pr.118.015651 |
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