Biotin Derivatives
Items 111 to 118 of 118 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
(+)-Biotin Methyl Ester | 608-16-2 | sc-503565 | 10 mg | $388.00 | ||
(+)-Biotin Methyl Ester is a distinctive biotin derivative featuring a methyl ester functional group that enhances its lipophilicity and membrane permeability. This compound exhibits unique molecular interactions with carboxylate groups, promoting esterification reactions. Its reactivity profile allows for efficient conjugation with various biomolecules, influencing metabolic pathways. The compound's stability under physiological conditions supports its role in modulating biochemical processes, making it a versatile tool in biochemical research. | ||||||
Biotin Diacid | 57671-79-1 | sc-503566 sc-503566A sc-503566B | 10 mg 25 mg 50 mg | $2400.00 $4000.00 $6005.00 | ||
Biotin Diacid is a notable biotin derivative characterized by its dual carboxylic acid groups, which facilitate strong hydrogen bonding and ionic interactions. This compound exhibits enhanced solubility in aqueous environments, promoting its reactivity in esterification and amidation reactions. Its unique structural features enable selective binding to proteins, influencing enzymatic activity and metabolic regulation. The compound's stability and reactivity make it a significant player in biochemical pathways. | ||||||
D-Biotin Dimer Acid | 1163708-46-0 | sc-503568 | 10 mg | $13500.00 | ||
D-Biotin Dimer Acid is a distinctive biotin derivative featuring a unique dimeric structure that enhances its capacity for molecular recognition. The compound's carboxylic acid functionalities enable it to engage in diverse electrostatic interactions, promoting its role in complexation with metal ions. Its reactivity profile is marked by rapid ester formation, allowing for versatile applications in synthetic chemistry. Additionally, its hydrophilic nature contributes to its behavior in biological systems, influencing solubility and transport mechanisms. | ||||||
6-[4′-N-(biotinylaminopropyl-NHCOCH2-PEG2-acetyl)-aminophenyl]-hexane-2,4-dione | 1522299-17-7 | sc-503571 | 5 mg | $380.00 | ||
6-[4'-N-(biotinylaminopropyl-NHCOCH2-PEG2-acetyl)-aminophenyl]-hexane-2,4-dione is a sophisticated biotin derivative characterized by its multifunctional structure, which facilitates specific binding interactions. The presence of a PEG spacer enhances solubility and biocompatibility, while the hexane-2,4-dione moiety introduces unique reactivity, allowing for selective conjugation with various biomolecules. This compound's design promotes efficient molecular assembly and targeted delivery in complex biological environments. | ||||||
N-Biotinyl Dopamine | 241142-94-9 | sc-503572 sc-503572A | 10 mg 100 mg | $296.00 $2040.00 | ||
N-Biotinyl Dopamine is a versatile biotin derivative distinguished by its unique ability to engage in specific molecular interactions through its dopamine moiety. This compound exhibits enhanced stability and reactivity, enabling it to participate in diverse biochemical pathways. Its structural features facilitate the formation of dynamic complexes, promoting effective binding to target molecules. The integration of biotin enhances its affinity for avidin or streptavidin, making it a valuable tool for studying protein interactions and cellular processes. | ||||||
10-Benzyloxyethoxyphosphinyl-N-biotinamidopentyldecanamide | 1246814-51-6 | sc-503724 | 2.5 mg | $330.00 | ||
10-Benzyloxyethoxyphosphinyl-N-biotinamidopentyldecanamide is a distinctive biotin derivative characterized by its phosphinyl group, which enhances its reactivity and facilitates unique molecular interactions. This compound exhibits a robust capacity for forming stable conjugates, allowing for selective targeting in biochemical assays. Its structural design promotes efficient binding to biotin-binding proteins, enabling intricate studies of molecular dynamics and cellular mechanisms. | ||||||
Biotinyl Tyramide | 41994-02-9 | sc-503573 | 100 mg | $400.00 | ||
Biotinyl Tyramide is a biotin derivative characterized by its unique tyramide structure, which enhances its reactivity through the formation of covalent bonds with amine groups in proteins. This compound exhibits a high affinity for biotin-binding proteins, facilitating specific molecular interactions that can influence cellular pathways. Its distinct properties allow for efficient labeling and detection in various biochemical assays, showcasing its role in enhancing signal amplification through enzymatic reactions. | ||||||
N-Biotinyl p-Aminophenyl Arsinic Acid | 212391-23-6 | sc-503570B sc-503570 sc-503570A sc-503570C sc-503570D | 2 mg 5 mg 10 mg 25 mg 50 mg | $199.00 $352.00 $617.00 $1385.00 $2453.00 | ||
N-Biotinyl p-Aminophenyl Arsinic Acid is a biotin derivative characterized by its unique arsinic acid moiety, which facilitates specific interactions with biomolecules. This compound exhibits distinct reactivity patterns, particularly in nucleophilic substitution reactions, due to the presence of the amino group. Its structural features enable selective binding to proteins, potentially influencing cellular pathways. Additionally, its solubility in polar solvents enhances its compatibility in diverse chemical environments, affecting its overall behavior in various applications. | ||||||