Bis-PEG7-NHS ester is a bifunctional polyethylene glycol (PEG) linker bearing two N-hydroxysuccinimide (NHS) ester termini, enabling efficient conjugation to primary amines on PROTAC-relevant ligands such as lysine residues, amine-functionalized small molecules, or engineered binding domains. Structurally, it provides a flexible, hydrophilic PEG chain architecture with two reactive NHS groups positioned to facilitate intramolecular or intermolecular coupling, allowing researchers to tune linker length and accessibility while minimizing steric hindrance and aggregation. In PROTAC design, this linker serves as a modular “bridge” that connects an amine-bearing targeting moiety to a second component (e.g., an E3 ligase ligand) through stable amide bond formation, thereby promoting productive ternary complex assembly and controlled proximity between the recruited proteins. Its value lies in improving conjugation efficiency and solubility, supporting systematic linker optimization to enhance targeted protein degradation performance in experimental workflows.
Structure of 1334170-02-3
* For research and manufacturing use only. Not for human or clinical use.
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This PROTAC linker product, Bis-PEG7-NHS ester, provides a bifunctional polyethylene glycol (PEG) scaffold capped with N-hydroxysuccinimide (NHS) ester groups for efficient conjugation. Its flexible, hydrophilic linker architecture supports favorable solubility and reduced nonspecific interactions in targeted protein degradation workflows. The dual NHS reactivity enables modular assembly of PROTACs by connecting two ligands or a ligand to a scaffold, facilitating systematic optimization. Detailed structural and reactivity guidance is provided below.
Structure: Bis-PEG7-NHS ester is a PEG-based linker containing two NHS ester termini, connected through ether-rich PEG chains. It features amide-forming activated carbonyls and stable ethyl/alkyl substituent environments typical of NHS esters. The overall structure is flexible, water-compatible, and designed for bioconjugation.
Reactivity: The NHS ester groups react with primary amines to form stable amide bonds via nucleophilic acyl substitution. Suitable conditions typically use mildly basic aqueous buffers that preserve NHS ester reactivity while promoting amine nucleophilicity. Common approaches include adding the amine-containing ligand under controlled pH and temperature, using compatible solvents such as aqueous buffer with limited cosolvent if needed. No special catalysts are generally required; reaction monitoring is recommended to manage hydrolysis of NHS esters.
* 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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