DBCO-PEG4-alcohol

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DBCO-PEG4-alcohol

DBCO-PEG4-alcohol | 1416711-60-8

Catalog Number R01-0379
Category Cycloalkyne Dyes (DBCO)
Molecular Formula C₂₉H₃₆N₂O₆
Molecular Weight 508.61
Catalog Number Size Price Quantity
R01-0379 -- $--

Product Introduction

DBCO-PEG4-alcohol is a polyethylene glycol (PEG)-based PROTAC linker. DBCO-PEG4-alcohol can be used in the synthesis of a series of PROTACs.

Chemical Information

Synonyms Dibenzoazacyclooctyne-tetra(ethylene glycol);6-(2-azatricyclo[10.4.0.04,9]hexadeca-1(16),4,6,8,12,14-hexaen-10-yn-2-yl)-N-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethyl]-6-oxohexanamide; Hydroxy-PEG4-DBCO; DBCO-PEG(4)-OH; Dibenzocyclooctyne-PEG4-alcohol, for Copper-free Click Chemistry;6-{2-azatricyclo[10.4.0.0,hexadeca-1(16),4,6,8,12,14-hexaen-10-yn-2-yl}-N-(2-{2-[2-(2-hydroxyethoxy)ethoxy]ethoxy}ethyl)-6-oxohexanamide
Purity 95%
IUPAC Name 6-(2-azatricyclo[10.4.0.04,9]hexadeca-1(16),4,6,8,12,14-hexaen-10-yn-2-yl)-N-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethyl]-6-oxohexanamide
Canonical SMILES C1C2=CC=CC=C2C#CC3=CC=CC=C3N1C(=O)CCCCC(=O)NCCOCCOCCOCCO
InChI InChI=1S/C29H36N2O6/c32-16-18-36-20-22-37-21-19-35-17-15-30-28(33)11-5-6-12-29(34)31-23-26-9-2-1-7-24(26)13-14-25-8-3-4-10-27(25)31/h1-4,7-10,32H,5-6,11-12,15-23H2,(H,30,33)
InChI Key ZZXWONCQAFVJHM-UHFFFAOYSA-N
  • Product Specification
  • Application
Storage Please store the product under the recommended conditions in the Certificate of Analysis.

DBCO-PEG4-alcohol, a versatile chemical linker with widespread applications in biochemical and biomedical fields, serves as a key component in various cutting-edge applications. Here are four key applications:

Bioconjugation: At the forefront of bioconjugation techniques, DBCO-PEG4-alcohol plays a pivotal role in linking biomolecules such as proteins, peptides, and antibodies through the ingenious mechanism of copper-free click chemistry. This groundbreaking approach enables the precise and selective conjugation of biomolecules without resorting to cytotoxic copper catalysts, revolutionizing the creation of targeted therapeutic agents and diagnostic tools with unparalleled precision.

Drug Delivery: In the realm of drug delivery systems, DBCO-PEG4-alcohol shines as a game-changer by facilitating the functionalization of drug carriers like nanoparticles and liposomes with targeting ligands. This strategic enhancement optimizes the delivery and uptake of therapeutic agents exclusively to afflicted cells, minimizing off-target effects and heightening treatment efficacy. Moreover, the process of PEGylation extends the circulation time of drug carriers in the bloodstream, further elevating the efficiency of drug delivery systems.

Imaging and Diagnostics: Embarking on the frontier of molecular imaging and diagnostics, DBCO-PEG4-alcohol emerges as a critical component in the development of innovative molecular imaging probes and diagnostic assays. Through the conjugation of imaging agents such as fluorescent dyes or radioactive isotopes to targeting molecules via DBCO-PEG4-alcohol linkers, researchers achieve unparalleled specificity in imaging biological tissues and disease sites, facilitating early disease diagnosis and precise monitoring of disease progression with unparalleled precision.

Surface Functionalization: In the realm of surface functionalization, DBCO-PEG4-alcohol stands out as a transformative tool utilized to modify the surfaces of biomaterials and medical devices, enhancing their biocompatibility and functionality with remarkable efficacy. By anchoring bioactive molecules like cell-adhesion peptides or anti-fouling agents to these surfaces, tailored to diverse biomedical applications such as tissue engineering and implantable devices, this modification ensures seamless integration with biological systems while minimizing adverse reactions, paving the way for enhanced performance and biocompatibility in transformative biomedical applications.

Computed Properties

XLogP3 1.6
Hydrogen Bond Donor Count 2
Hydrogen Bond Acceptor Count 6
Rotatable Bond Count 16
Exact Mass 508.25733687 g/mol
Monoisotopic Mass 508.25733687 g/mol
Topological Polar Surface Area 97.3Ų
Heavy Atom Count 37
Formal Charge 0
Complexity 747
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
Covalently-Bonded Unit Count 1
Compound Is Canonicalized Yes
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