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 |
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R01-0379 | -- | $-- |
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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 |
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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 | |
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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 |
Applications of Fluorescent Probes & Dyes
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