m-PEG6-2-methylacrylate is a methoxy-terminated polyethylene glycol (PEG) linker bearing a 2-methylacrylate (methacrylate) ester at one end, providing a defined, flexible hydrophilic chain that can be readily incorporated into PROTAC architectures. Structurally, the PEG segment acts as a solubilizing spacer that reduces steric interference between the ligand-binding domains and can improve aqueous handling and effective conjugation. The terminal methacrylate group is designed for covalent attachment via polymerizable or Michael-type reactivity with appropriate nucleophiles or partner handles, enabling stable tethering to complementary functional groups used in bifunctional degraders. In targeted protein degradation research, such linkers help tune linker length and rigidity, thereby modulating ternary complex formation and degradation potency. This reagent is valuable for constructing PROTACs and related conjugates where controlled, end-functional PEG spacing is required to balance solubility, conjugation efficiency, and bioactive geometry.
Structure of 90784-86-4
* For research and manufacturing use only. Not for human or clinical use.
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m-PEG6-2-methylacrylate is a polyethylene glycol (PEG)-based PROTAC linker building block designed to provide solubility, conformational flexibility, and a reactive handle for efficient conjugation. Its ester-functional acrylate motif enables formation of well-defined linker–ligand connections under standard bioconjugation conditions, supporting the modular assembly of targeted protein degraders. The structural and reactivity features summarized below will be described in detail to guide experimental design and synthesis planning.
Structure: The linker comprises a PEG ether backbone terminating in a 2-methylacrylate ester, offering a hydrophilic, flexible scaffold. It contains ether linkages along the chain and an activated α,β-unsaturated ester moiety capable of participating in conjugation reactions. The overall polarity supports aqueous compatibility.
Reactivity: The 2-methylacrylate group is suited for nucleophilic addition or Michael-type conjugation strategies commonly used to install PEG-based linkers onto amine- or thiol-containing partners. Typical approaches employ mild bases or nucleophiles in compatible organic/aqueous solvent mixtures to promote controlled coupling while minimizing side reactions. Reaction monitoring by chromatographic or spectroscopic methods is recommended to confirm consumption of the acrylate functionality.
* 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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