DBCO-PEG2-DBCO - CAS 2639395-48-3

DBCO-PEG2-DBCO - CAS 2639395-48-3 Catalog number: BADC-01671

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DBCO-PEG2-DBCO is a click chemistry reagent containing an azide group.

Category
ADCs Linker
Product Name
DBCO-PEG2-DBCO
CAS
2639395-48-3
Catalog Number
BADC-01671
Molecular Formula
C44H42N4O6
Molecular Weight
722.83
Purity
0.98
DBCO-PEG2-DBCO

Ordering Information

Catalog Number Size Price Quantity
BADC-01671 -- $-- Inquiry
Description
DBCO-PEG2-DBCO is a click chemistry reagent containing an azide group.
IUPAC Name
4-(2-azatricyclo[10.4.0.04,9]hexadeca-1(16),4,6,8,12,14-hexaen-10-yn-2-yl)-N-[2-[2-[2-[[4-(2-azatricyclo[10.4.0.04,9]hexadeca-1(16),4,6,8,12,14-hexaen-10-yn-2-yl)-4-oxobutanoyl]amino]ethoxy]ethoxy]ethyl]-4-oxobutanamide
Canonical SMILES
C1C2=CC=CC=C2C#CC3=CC=CC=C3N1C(=O)CCC(=O)NCCOCCOCCNC(=O)CCC(=O)N4CC5=CC=CC=C5C#CC6=CC=CC=C64
InChI
InChI=1S/C44H42N4O6/c49-41(21-23-43(51)47-31-37-13-3-1-9-33(37)17-19-35-11-5-7-15-39(35)47)45-25-27-53-29-30-54-28-26-46-42(50)22-24-44(52)48-32-38-14-4-2-10-34(38)18-20-36-12-6-8-16-40(36)48/h1-16H,21-32H2,(H,45,49)(H,46,50)
InChIKey
GPRBYNSGOSAHPU-UHFFFAOYSA-N
Shipping
Ambient temperature
Storage
-20°C

DBCO-PEG2-DBCO, a versatile bifunctional molecule highly prevalent in bioconjugation applications, plays a pivotal role in enabling the precise modification and cross-linking of biomolecules with exceptional specificity. Here are four key applications of DBCO-PEG2-DBCO:

Protein Labeling: Leveraging the potent capabilities of DBCO-PEG2-DBCO in protein labeling facilitates the conjugation of biomolecules, such as antibodies or enzymes, to fluorescent dyes or other alternative labels. This intricate process utilizes strain-promoted alkyne-azide cycloaddition (SPAAC), a copper-free click chemistry reaction, ensuring swift and effective bioconjugation. The incorporation of a PEG spacer mitigates steric hindrance, enhancing bioconjugation efficiency while preserving the proteins’ functionality with precision and finesse.

Drug Delivery Systems: In the realm of advanced drug delivery systems, DBCO-PEG2-DBCO emerges as a critical tool for the covalent attachment of therapeutic agents to nanoparticles or polymers. PEGylation contributes to enhancing the solubility and stability of the drug complex, while the DBCO groups enable specific and efficient conjugation. This cutting-edge method holds the potential to revolutionize targeted delivery, mitigating systemic side effects associated with therapeutic compounds in a manner that is both innovative and transformative.

Biomaterials Engineering: The indispensable role of DBCO-PEG2-DBCO in biomaterials engineering cannot be understated. This multifaceted molecule plays a pivotal role in crafting functionalized biomaterials tailored for tissue engineering and regenerative medicine. By linking bioactive molecules, such as growth factors or adhesion peptides, to scaffolds, researchers can engineer materials that promote cell attachment, proliferation, and differentiation. The controlled and site-specific conjugation guarantees uniform bioactivity throughout the material, ushering in groundbreaking advancements in the field with complexity and variability.

Diagnostics: Transitioning into the realm of diagnostics, DBCO-PEG2-DBCO emerges as a disruptive force facilitating the attachment of capture agents, like antibodies or aptamers, onto sensor surfaces. This bioconjugation process enhances the sensitivity and specificity of biosensors employed in detecting biomarkers or pathogens, thereby reshaping diagnostic capabilities. The incorporation of a PEG linker introduces flexibility and reduces non-specific binding, culminating in precise and reliable diagnostic outcomes that are at the forefront of driving innovation in the diagnostics arena with intricacy and diversity.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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