Propargyl-aliphatic-NHS ester contains a propargyl functional group (-C≡CH) attached to the aliphatic carbon chain.
The propargyl group is known for its ability to undergo click chemistry reactions, which is a powerful tool for the bioconjugation of molecules. The aliphatic NHS ester functional group enables the selective and efficient attachment of propargyl-aliphatic-NHS ester to amine groups on proteins, peptides, and other biomolecules, through formation of amide bonds.
Propargyl-aliphatic-NHS ester has been extensively utilized in the development of novel bioconjugates for drug delivery and targeting applications. Its unique chemical properties allow for the covalent attachment of therapeutic agents to biomolecules, through click chemistry reactions. The resulting conjugates exhibit improved stability, increased selectivity, and enhanced therapeutic efficacy in vivo, leading to reduced side effects and improved patient outcomes.
Propargyl-aliphatic-NHS ester
| Cat# | Name | Structure | Pricing |
|---|---|---|---|
| AP13717 | 5-Hexynoic Acid-NHS Ester | Pricing | |
| AP14316 | 2,5-Dioxopyrrolidin-1-yl hept-6-ynoate | Pricing |
