Biotin Derivatives

1-Biotinylamino-3,6,9-trioxaundecane-11-yl-methanethiosulfonate is a distinctive biotin derivative characterized by its unique trioxaundecane backbone, which enhances solubility and stability in aqueous environments. This compound features a methanethiosulfonate group that facilitates selective thiol reactions, promoting efficient bioconjugation. Its structural design allows for versatile interactions with biomolecules, enabling tailored applications in biochemical assays and research.

Sulfo-N-succinimidyl 6-(biotinamido) hexanoate, sodium salt is a specialized biotin derivative known for its robust amine-reactive properties. The sulfo-N-succinimidyl group enhances the compound's reactivity towards primary amines, facilitating efficient conjugation to proteins and other biomolecules. Its hexanoate linker provides flexibility, allowing for optimal spatial orientation in binding interactions. This compound's unique design promotes stable biotinylation, crucial for various biochemical applications.

2-{N2-[N6-(4-Azido-2,3,5,6-tetrafluorobenzoyl)-6-aminocaproyl]-N6-(6-biotinamidocaproyl)-L-lysinylamido}] Ethyl 2-Carboxyethyl Disulfide is a sophisticated biotin derivative characterized by its dual functionality and unique disulfide linkage. The azido group enables selective click chemistry, facilitating targeted modifications. Its biotin moiety ensures strong affinity for avidin or streptavidin, enhancing detection and isolation processes. The ethyl carboxyethyl component contributes to solubility and stability, promoting versatile applications in biochemical research.

2-[N2-(4-Azido-2,3,5,6-tetrafluorobenzoyl)-N6-(6-biotinamidocaproyl)-L-lysinyl]ethyl Methanethiosulfonate is a distinctive biotin derivative featuring a methanethiosulfonate group that enables site-specific conjugation through thiol-reactive chemistry. The azido functionality allows for efficient click reactions, enhancing molecular labeling and tracking. Its biotin component provides robust binding to streptavidin, facilitating purification and detection in complex biological systems. The compound's unique structure promotes stability and reactivity, making it a valuable tool in biochemical assays.

DY-550-biotin is a specialized biotin derivative characterized by its unique fluorophore properties, which enable enhanced fluorescence for sensitive detection applications. The compound exhibits strong affinity for streptavidin, ensuring effective bioconjugation. Its distinct molecular architecture allows for versatile interactions with biomolecules, facilitating the study of protein dynamics and cellular processes. The compound's stability under various conditions further enhances its utility in experimental setups.

Photobiotin acetate salt is a distinctive biotin derivative known for its photoreactive properties, which enable covalent bonding upon exposure to light. This compound features a unique structure that facilitates specific interactions with biomolecules, enhancing its utility in probing cellular mechanisms. Its reactivity profile allows for selective labeling and tracking of proteins, making it a valuable tool in biochemical research. Additionally, its solubility characteristics support diverse experimental conditions.

(+)-Biotin-(PEO)3-iodoacetamide is a specialized biotin derivative characterized by its polyethylene oxide (PEO) chain, which enhances solubility and biocompatibility. This compound exhibits unique reactivity through its iodoacetamide group, enabling efficient conjugation to thiol-containing biomolecules. Its distinct molecular architecture promotes specific interactions with proteins, facilitating targeted labeling and analysis in biochemical studies. The PEO segment also contributes to improved stability and reduced non-specific binding in complex biological environments.

1-Biotinylamino-3,6,9-trioxaundecane-11-bromide is a distinctive biotin derivative featuring a trioxaundecane backbone that enhances its solubility and stability in aqueous environments. The bromide moiety introduces unique reactivity, allowing for selective nucleophilic substitution reactions. This compound's structure facilitates strong interactions with avidin and streptavidin, promoting efficient biotinylation in various biochemical applications. Its design supports versatile conjugation strategies, making it a valuable tool for probing molecular interactions.

Acriflavin-Biotin Conjugate is a novel biotin derivative characterized by its dual functionality, combining the properties of acriflavin with biotin. This conjugate exhibits unique photophysical properties, enabling specific light-induced reactions. Its structure promotes enhanced binding affinity to biotin-binding proteins, facilitating targeted interactions. The conjugate's distinct electron-donating characteristics may influence reaction kinetics, making it a compelling candidate for exploring complex biochemical pathways.

Biotinamido Poly(ethylene glycol)1000 is a versatile biotin derivative characterized by its unique polymeric structure, which enhances solubility and biocompatibility. The PEG component facilitates hydrophilic interactions, promoting effective molecular recognition and binding. This compound exhibits distinct kinetic behavior in conjugation reactions, allowing for tailored modifications in biochemical applications. Its ability to form stable complexes with biomolecules underscores its potential in diverse biochemical contexts.