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Home  > L-Lysine,N2-[3-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)-1-oxopropyl]-N6-[5-[(3aS,4S,6aR)-hexahydro-2-oxo-1H-thieno[3,4-d]imidazol-4-yl]-1-oxopentyl]-

AW55091

102849-12-7 | L-Lysine,N2-[3-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)-1-oxopropyl]-N6-[5-[(3aS,4S,6aR)-hexahydro-2-oxo-1H-thieno[3,4-d]imidazol-4-yl]-1-oxopentyl]-

Packsize Purity Availability Price Discounted Price    Quantity
1mg 80% in stock $21.00 $15.00 -   +
5mg 80% in stock $36.00 $26.00 -   +
10mg 80% in stock $61.00 $43.00 -   +
50mg 80% in stock $193.00 $135.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AW55091
Chemical Name: L-Lysine,N2-[3-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)-1-oxopropyl]-N6-[5-[(3aS,4S,6aR)-hexahydro-2-oxo-1H-thieno[3,4-d]imidazol-4-yl]-1-oxopentyl]-
CAS Number: 102849-12-7
Molecular Formula: C23H33N5O7S
Molecular Weight: 523.6024
MDL Number: MFCD00467354
SMILES: O=C(CCCC[C@@H]1SC[C@H]2[C@@H]1NC(=O)N2)NCCCC[C@@H](C(=O)O)NC(=O)CCN1C(=O)C=CC1=O

 

Upstream Synthesis Route
  • 3-(N-Maleimidylpropionyl)biocytin is a specialized chemical compound that finds extensive application in chemical synthesis, specifically in the field of bioconjugation. Due to its unique structure, this compound is highly reactive towards thiol groups, making it an ideal tool for the precise and selective modification of biomolecules such as proteins and peptides.In chemical synthesis, 3-(N-Maleimidylpropionyl)biocytin is commonly used for the crosslinking of sulfhydryl-containing molecules, enabling the creation of stable covalent bonds between different biomolecules. By exploiting the maleimide moiety present in the compound, researchers can selectively target and label specific proteins or peptides for various analytical or therapeutic purposes.Moreover, the biotin moiety in 3-(N-Maleimidylpropionyl)biocytin offers additional functionalities, allowing for the attachment of streptavidin or avidin-linked probes for subsequent detection or purification steps. This biotin-streptavidin interaction is widely employed in bioconjugation strategies and molecular biology techniques, further expanding the versatility of this compound in chemical synthesis applications.
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