| Identification | Back Directory | [Name]
BocNH-PEG7-CH2CH2N3 | [CAS]
206265-96-5 | [Synonyms]
Azido-PEG7-NHBoc
Boc-NH-PEG7-azide
BocNH-PEG7-CH2CH2N3
Boc-N-Amido-PEG7-N3 | [Molecular Formula]
C21H42N4O9 | [MDL Number]
MFCD30723222 | [MOL File]
206265-96-5.mol | [Molecular Weight]
494.59 |
| Hazard Information | Back Directory | [Description]
t-boc-N-amido-PEG7-azide is a PEG molecule with an azide(N3) group and Boc-protected amino group. The hydrophilic PEG spacer increases solubility in aqueous media. The azide group is reactive with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage. The Boc group can be deprotected under mild acidic conditions to form the free amine. | [Uses]
Boc-NH-PEG7-azide is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. Boc-NH-PEG7-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]
PEGs | [References]
[1] An S, et al. Small-molecule PROTACs: An emerging and promising approach for the development of targeted therapy drugs. EBioMedicine. 2018 Oct;36:553-562 DOI:10.1016/j.ebiom.2018.09.005 |
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