VH 032-linker 6 is a high-quality E3 Ligase Ligand-Linker Conjugate specifically designed for use in PROTAC (Proteolysis Targeting Chimera) drug discovery and development. Featuring a VH032 derivative as the VHL (Von Hippel-Lindau) E3 ligase ligand, this compound is covalently linked to a customizable linker, providing an ideal foundation for building PROTAC molecules. VH 032-linker 6 enables researchers to selectively recruit the VHL E3 ubiquitin ligase, thereby facilitating the targeted degradation of protein targets via the ubiquitin-proteasome system. Suitable for projects aiming at the degradation of disease-relevant proteins, this conjugate streamlines the process of PROTAC assembly, allowing for rapid optimization and development of next-generation therapeutics for oncology, neurodegenerative diseases, and beyond. As a specialized molecular tool, VH 032-linker 6 empowers academic and pharmaceutical scientists pursuing targeted protein degradation strategies.
Structure of 2098799-80-3
* For research and manufacturing use only. Not for human or clinical use.
| Size | Price | Stock | Quantity |
|---|---|---|---|
| 200 mg | $1099 | In stock |
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Background Introduction
VH 032-linker 6 is a specialized E3 ligase ligand-linker conjugate designed for use in PROTAC (Proteolysis Targeting Chimera) drug development. It is based on the widely studied VH032 ligand, which selectively binds to the von Hippel-Lindau (VHL) E3 ubiquitin ligase—a key component for targeted protein degradation strategies. The addition of a tailored linker moiety enables effective conjugation to various target protein ligands, making VH 032-linker 6 an essential building block for next-generation chemical biology tools and therapeutic agents.
Mechanism
VH 032-linker 6 works by harnessing the natural protein degradation pathway of the ubiquitin-proteasome system. The VH032 moiety specifically binds to the VHL E3 ubiquitin ligase, while the attached linker provides a customizable functional handle. When incorporated into bifunctional PROTAC molecules, VH 032-linker 6 allows the simultaneous recruitment of VHL and a protein of interest. This brings the target protein into proximity with the E3 ligase, facilitating ubiquitination and subsequent proteasomal degradation, thereby selectively removing disease-causing or unwanted proteins from the cell.
Applications
VH 032-linker 6 is utilized extensively in PROTAC molecule synthesis, especially for targeting 'undruggable' proteins in oncology, neurodegenerative, and autoimmune diseases. It enables researchers to design and optimize bifunctional degraders for high-throughput screening, mechanistic studies, and preclinical drug discovery. Furthermore, VH 032-linker 6 is ideal for developing tool compounds for studying protein function, validating therapeutic targets, and advancing structure-activity relationship (SAR) analyses within the rapidly evolving field of targeted protein degradation.
* 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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