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Tri-GalNAc-DBCO

Copper-free clickable Tri-GalNAc identifier for target delivery

Size Catalog No. Price
5 mg BCFA-245-5  580,00
10 mg BCFA-245-10  990,00
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Chemical Properties

  • Molecular Formula

    C82H127N11O29

  • Shelf Life

    12 months unopened after receipt

  • Storage Conditions

    20 °C, dark

  • Molecular Weight

    1730.94 g/mol

  • Purity

    ≥ 98% (HPLC)

  • Physical State

    white to off-white solid

  • CAS Number

    n.a.

  • Solubility

    H2O, DMSO

  • Preparation/Handling

    For a 10 mM solution add 289 μL to 5 mg.
    For a 10 mM solution add 578 μL to 10 mg.

Product Information

Tri-GalNAc-DBCO: Advanced Liver-Targeting Conjugation Reagent

Tri-GalNAc-DBCO is a synthetic molecule combining three N-acetylgalactosamine (GalNAc) residues with dibenzocyclooctyne (DBCO). This design enables high-affinity hepatocyte targeting via the asialoglycoprotein receptor (ASGPR) and bioorthogonal click chemistry through strain-promoted alkyne-azide cycloaddition (SPAAC). It allows efficient conjugation to azide-functionalized biomolecules such as nucleic acids, proteins, and therapeutic agents.

Tri-GalNAc-DBCO modified oligonucleotide

Why use Tri-GalNAc-DBCO for Liver-Specific Delivery

Conventional drug delivery systems often face challenges like low hepatocyte uptake, non-specific targeting, and limited RNA therapeutic efficiency. Tri-GalNAc-DBCO addresses these limitations by combining GalNAc-mediated receptor targeting with copper-free click chemistry, ensuring selective delivery and safe conjugation.

Key Features

  • Trivalent GalNAc structure for strong ASGPR binding
  • DBCO functionality for copper-free SPAAC click chemistry
  • Bioorthogonal and catalyst-free for in vivo compatibility
  • High purity and stability for reproducible results

Tri-GalNAc-DBCO application

Applications

Tri-GalNAc-DBCO has several practical applications, particularly in bioconjugation and targeted protein degradation:

  1. siRNA and RNA Therapeutics: Improves delivery for RNA interference and gene silencing
  2. Protein and Antibody Conjugation: Enables liver-specific delivery of biologics
  3. Targeted Prodrug Development: Supports controlled activation in hepatocytes
  4. Extracellular Protein Degradation: Facilitates LYTAC and targeted protein degradation strategies
  5. Bioconjugation via Click Chemistry: Enables precise, catalyst-free conjugation for research and drug development

How It Works

Tri-GalNAc-DBCO leverages ASGPR-mediated endocytosis for selective hepatocyte uptake, reducing off-target effects and improving therapeutic efficiency. Its DBCO group enables copper-free click chemistry, making it suitable for sensitive biological systems and scalable drug development.

baseclick: Your Partner for GalNAc-siRNA Conjugates

In addition to Tri-GalNAc-DBCO, baseclick offers custom GalNAc-siRNA conjugation services with exceptional purity and scalability, supporting preclinical research and therapeutic development.

 

LITERATURE

Site-Selective LYTACs for Targeted Protein Degradation, D. Trauner et al., 2021, Synfacts, Vol. 17(07), 0818.

https://doi.org/10.1055/s-0040-1719647

LYTACs that engage the asialoglycoprotein receptor for targeted protein degradation, G. Ahn et al., 2021, Nature Chemical Biology, Vol. 17(9), p. 937-946.

https://doi.org/10.1038/s41589-021-00770-1

Targeting the Epidermal Growth Factor Receptor with Molecular Degraders: State-of-the-Art and Future Opportunities, P. Maity et al., 2023, Journal of Medicinal Chemistry, Vol. 66(5), p. 3135-3172.

https://doi.org/10.1021/acs.jmedchem.2c01242

Targeted Strategies for Degradation of Key Transmembrane Proteins in Cancer, V. Sakanyan et al., 2023, Biotech, Vol.12, p. 57.

https://pubmed.ncbi.nlm.nih.gov/37754201/

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