DBCO-CONH-S-S-NHS ester - CAS 1435934-53-4

DBCO-CONH-S-S-NHS ester - CAS 1435934-53-4 Catalog number: BADC-00952

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Category
ADCs Linker
Product Name
DBCO-CONH-S-S-NHS ester
CAS
1435934-53-4
Catalog Number
BADC-00952
Molecular Formula
C27H46N4O7S
Molecular Weight
570.74
Purity
>95.0%

Ordering Information

Catalog Number Size Price Quantity
BADC-00952 -- $-- Inquiry
Synonyms
DBCO-CONH-S-S-COONHS ester; Azadibenzocyclooctyne-S-S-NHS ester
Canonical SMILES
C1CC(=O)N(C1=O)OC(=O)CCSSCCNC(=O)CCC(=O)N2CC3=CC=CC=C3C#CC4=CC=CC=C42
InChI
InChI=1S/C28H27N3O6S2/c32-24(29-16-18-39-38-17-15-28(36)37-31-26(34)13-14-27(31)35)11-12-25(33)30-19-22-7-2-1-5-20(22)9-10-21-6-3-4-8-23(21)30/h1-8H,11-19H2,(H,29,32)
InChIKey
RPNGUSKTYYIUDE-UHFFFAOYSA-N
Solubility
10 mm in DMSO
Shelf Life
0-4°C for short term (days to weeks), or -20°C for long term (months).
Shipping
Room temperature, or blue ice upon request.
Storage
Store at 4 °C

DBCO-CONH-S-S-NHS ester, a versatile bifunctional reagent, plays a pivotal role in the realms of bioconjugation and click chemistry. Delve into its diverse applications:

Bioconjugation: Serving as a precise biomolecule linker, DBCO-CONH-S-S-NHS ester emerges as a crucial tool in connecting antibodies or peptides to diverse surfaces or biomolecules. The DBCO moiety intricately engages azide groups in a bioorthogonal manner, facilitating swift and selective conjugation while upholding native biological processes. This method is indispensable for constructing targeted drug delivery systems and diagnostic assays.

Protein Labeling: Capitalizing on the NHS ester group, DBCO-CONH-S-S-NHS ester selectively interacts with primary amines on proteins, enabling efficient labeling and tracking both in vitro and in vivo. This capability is essential for probing protein dynamics, interactions, and localization within cellular milieus. Proteins can be embellished with fluorescent dyes or other tags, ushering in diverse imaging applications with profound implications for cutting-edge research initiatives.

Surface Functionalization: Harnessing the potency of DBCO-CONH-S-S-NHS ester, surfaces such as nanoparticles or biosensors can undergo functionalization by appending bioactive molecules. This strategic maneuvering facilitates the development of high-sensitivity biosensors adept at detecting specific biomolecules with extraordinary accuracy and specificity. The utilization of DBCO-CONH-S-S-NHS ester in surface functionalization also extends to bioseparation technologies, enabling the selective capture and isolation of target molecules.

Drug Development: Positioned as a game-changer in the realm of drug development, DBCO-CONH-S-S-NHS ester empowers the creation of prodrugs or conjugates that heighten therapeutic agent delivery and efficacy. Through the coupling of drugs with targeting moieties, researchers achieve precise site-specific drug delivery, consequently minimizing off-target effects and substantially enhancing therapeutic outcomes. This innovative approach not only bolsters the stability and bioavailability of pharmacologically active compounds but also unlocks new vistas for personalized medicine endeavors.

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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