N-(Azido-PEG3)-N-bis(PEG3-acid) HCl salt

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N-(Azido-PEG3)-N-bis(PEG3-acid) HCl salt Basic information
Product Name:N-(Azido-PEG3)-N-bis(PEG3-acid) HCl salt
Synonyms:N-(Azido-PEG3)-N-bis(PEG3-acid) HCl salt;ZUN 42572;N3-PEG3-N-(PEG3-COOH)2;13-(2-(2-(2-(2-azidoethoxy)ethoxy)ethoxy)ethyl)-4,7,10,16,19,22-hexaoxa-13-azapentacosanedioic acid
CAS:2055042-57-2
MF:C26H50N4O13
MW:626.7
EINECS:
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Mol File:2055042-57-2.mol
N-(Azido-PEG3)-N-bis(PEG3-acid) HCl salt Structure
N-(Azido-PEG3)-N-bis(PEG3-acid) HCl salt Chemical Properties
Safety Information
MSDS Information
N-(Azido-PEG3)-N-bis(PEG3-acid) HCl salt Usage And Synthesis
DescriptionN-(Azido-PEG3)-N-bis(PEG3-acid) HCl salt is a click chemistry branched molecule. It enables PEGylation via Click Chemistry. The terminal carboxylic acids can react with primary amino groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.
UsesN-(Azido-PEG3)-N-bis(PEG3-acid) is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. N-(Azido-PEG3)-N-bis(PEG3-acid) 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 50PEGs
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
N-(Azido-PEG3)-N-bis(PEG3-acid) HCl salt Preparation Products And Raw materials
Tag:N-(Azido-PEG3)-N-bis(PEG3-acid) HCl salt(2055042-57-2) Related Product Information
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