m-PEG3-AcS is a short, methoxy-terminated polyethylene glycol linker bearing an acylthio (AcS) functional group, enabling controlled attachment of thiol-reactive handles used in targeted protein degradation workflows. Structurally, it consists of a three–ethylene glycol unit PEG chain that provides aqueous solubility and conformational flexibility, while the terminal thioester/AcS motif serves as a chemically versatile linkage site for installing or exchanging conjugation partners through thiol-mediated chemistry. In PROTAC design, such PEG linkers help tune the effective distance and orientation between the ligand-binding moieties and the E3 ligase recruiter, reducing steric clashes and improving productive ternary complex formation. The AcS functionality further supports modular synthesis strategies for constructing degraders, facilitating rapid generation of analogs for structure–activity relationship studies. Overall, m-PEG3-AcS is valuable for researchers seeking reproducible, water-compatible linker chemistry to optimize conjugation geometry and degradation performance in targeted protein degradation experiments.
Structure of 857284-78-7
* For research and manufacturing use only. Not for human or clinical use.
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m-PEG3-AcS is a polyethylene glycol-based linker designed to support efficient conjugation strategies used in PROTAC assembly. Its PEG character improves solubility and can help maintain productive spatial relationships between ligand modules, which is important for targeted protein degradation workflows. The acyl-sulfide functionality enables practical coupling to generate stable PROTAC architectures.
Structure: The linker is a PEG-derived chain bearing an acyl-sulfide motif, providing an ether-rich, flexible scaffold. It contains ether linkages along the PEG segment and a sulfur-containing thioester-like functionality, with a polar, hydrogen-bond-accepting environment that supports aqueous compatibility and conformational mobility.
Reactivity: m-PEG3-AcS is suitable for PROTAC linker construction where sulfide-containing intermediates are required. Conjugation is typically performed under controlled, anhydrous conditions to preserve the reactive sulfur functionality, using standard organic synthesis protocols for acyl-sulfide transformations. Mild base or nucleophilic activation may be used depending on the partner ligand, with polar aprotic solvents commonly employed to promote coupling and minimize 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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