mPEG9-amine is a methoxy-terminated poly(ethylene glycol) amine featuring an ether-linked PEG chain capped with a terminal primary amine, providing a flexible, hydrophilic spacer for bioconjugation. In PROTAC and targeted protein degradation workflows, this linker is commonly used to introduce a PEG segment that can improve aqueous solubility, reduce nonspecific interactions, and modulate the effective distance and orientation between the ligand-binding warhead and the recruited E3 ligase moiety. The terminal amine enables covalent coupling to activated carboxylic acids, activated esters, or other electrophilic intermediates, allowing researchers to assemble PROTACs or related bifunctional degraders with controlled linker attachment sites. Its use facilitates systematic structure–property studies, including tuning of linker length and hydrophilicity to optimize degradation potency, selectivity, and cellular uptake while maintaining synthetic accessibility for iterative medicinal chemistry.
Structure of 211859-73-3
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mPEG9-amine is an amine-terminated methoxy poly(ethylene glycol) building block designed to introduce a hydrophilic, flexible PEG spacer into PROTAC constructs. Its ether-rich backbone can improve aqueous solubility and reduce nonspecific interactions, while the terminal primary amine enables efficient conjugation to ligands or linker fragments used in targeted protein degradation workflows. The following sections describe its structural features and practical reactivity considerations in PROTAC assembly.
Structure: mPEG9-amine comprises a methoxy-terminated poly(ethylene glycol) chain capped with a primary amine. The molecule is dominated by ether linkages along the PEG backbone, with a terminal C–N bond defining the reactive handle. This architecture yields a flexible, highly solvated, hydrophilic polymer-like scaffold.
Reactivity: The terminal primary amine is suitable for standard amide or urea formation with activated carboxylic acids or isocyanates, and for carbamate formation using activated carbonyl reagents. Typical PROTAC linker coupling strategies employ coupling reagents such as carbodiimides with additives, or acyl chlorides/activated esters under anhydrous or buffered conditions. Polar aprotic solvents and controlled pH help maintain amine nucleophilicity while minimizing PEG degradation and side reactions.
* Our calculator is based on the following equation:
Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2
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