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Catalog Number:
02716
CAS Number:
252049-11-9
Nα-Fmoc-Nε-nicotinoyl-L-lysine
Purity:
98+%
Synonym(s):
Fmoc-L-Lys(nicotinoyl)-OH
Documents
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Product Information

Na-Fmoc-Ne-nicotinoyl-L-lysine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (9-fluorenylmethyloxycarbonyl) group, which facilitates the selective modification of the amino group, making it an essential building block in the synthesis of complex peptides. Its unique nicotinoyl moiety enhances solubility and stability, allowing for improved incorporation into various biochemical applications. Researchers in medicinal chemistry and biochemistry can leverage Na-Fmoc-Ne-nicotinoyl-L-lysine for the development of targeted therapeutics, particularly in the design of peptide-based drugs that require precise amino acid sequences for optimal activity.

The compound's ability to serve as a versatile intermediate in the synthesis of bioactive peptides makes it particularly valuable in pharmaceutical research. Its favorable properties, such as enhanced stability and solubility, provide significant advantages over similar compounds, allowing for more efficient synthesis processes. Na-Fmoc-Ne-nicotinoyl-L-lysine is ideal for applications in drug discovery, particularly in the development of novel therapeutics targeting specific biological pathways.

Synonyms
Fmoc-L-Lys(nicotinoyl)-OH
CAS Number
252049-11-9
Purity
98+%
Molecular Formula
C27H27N3O5
Molecular Weight
473.5
MDL Number
MFCD00080278
PubChem ID
68761798
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-L-Lys(nicotinoyl)-OH
CAS Number
252049-11-9
Purity
98+%
Molecular Formula
C27H27N3O5
Molecular Weight
473.5
MDL Number
MFCD00080278
PubChem ID
68761798
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Na-Fmoc-Ne-nicotinoyl-L-lysine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, enhancing the efficiency and yield of complex peptide chains.
  • Drug Development: Its unique structure allows for the design of novel therapeutic agents, especially in the field of cancer research, where targeted drug delivery systems are crucial.
  • Bioconjugation: The compound can be used to create bioconjugates, linking biomolecules for applications in diagnostics and therapeutics, improving specificity and effectiveness in targeting diseases.
  • Research on Protein Interactions: This chemical aids in studying protein-protein interactions, providing insights into cellular mechanisms and potential therapeutic targets in various diseases.
  • Modification of Amino Acids: It allows for the modification of lysine residues in proteins, which can be pivotal in understanding protein function and developing new protein-based therapies.

Citations