6-(2,5-Dioxo-2,5-dihydro-1H-pyrrol-1-yl)-N-((S)-1-(((S)-1-((4-(hydroxymethyl)phenyl)amino)-1-oxopropan-2-yl)amino)-3-methyl-1-oxobutan-2-yl)hexanamide

98%

Reagent Code: #107348
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CAS Number 1870916-87-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 486.56 g/mol
Formula C₂₅H₃₄N₄O₆
badge Registry Numbers
MDL Number MFCD32063500
inventory_2 Storage & Handling
Storage 2-8 ℃, inert gas storage

description Product Description

This compound is primarily utilized in the field of bioconjugation and protein modification. It serves as a versatile linker for attaching various molecules, such as peptides, proteins, or antibodies, to other functional groups or surfaces. Its reactive pyrrole dione moiety enables efficient coupling with thiol groups, making it valuable in the development of targeted drug delivery systems, diagnostic probes, and bioconjugate vaccines. Additionally, it is employed in the synthesis of complex biomolecules for research in biochemistry and molecular biology, particularly in studies involving protein-protein interactions and cellular labeling. Its design allows for precise control over conjugation, ensuring minimal disruption to the biological activity of the molecules involved.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days £106.12
inventory 100mg
10-20 days £174.80
inventory 250mg
10-20 days £297.06
6-(2,5-Dioxo-2,5-dihydro-1H-pyrrol-1-yl)-N-((S)-1-(((S)-1-((4-(hydroxymethyl)phenyl)amino)-1-oxopropan-2-yl)amino)-3-methyl-1-oxobutan-2-yl)hexanamide
This compound is primarily utilized in the field of bioconjugation and protein modification. It serves as a versatile linker for attaching various molecules, such as peptides, proteins, or antibodies, to other functional groups or surfaces. Its reactive pyrrole dione moiety enables efficient coupling with thiol groups, making it valuable in the development of targeted drug delivery systems, diagnostic probes, and bioconjugate vaccines. Additionally, it is employed in the synthesis of complex biomolecules for research in biochemistry and molecular biology, particularly in studies involving protein-protein interactions and cellular labeling. Its design allows for precise control over conjugation, ensuring minimal disruption to the biological activity of the molecules involved.
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