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Catalog Number:
47722
CAS Number:
2044709-77-3
Na-Fmoc-Ne-Boc-Ne-Methyl-D-lysine
Purity:
≥ 99.7% (Chiral HPLC)
Synonym(s):
Fmoc-D-Lys(Boc,Me)-OH
Documents
$185.00 /25MG
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Product Information

Na-Fmoc-Ne-Boc-Ne-Methyl-D-lysine is a versatile amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound features protective groups that enhance its stability and reactivity, making it an ideal choice for researchers focused on solid-phase peptide synthesis. Its unique structure allows for selective modifications, facilitating the incorporation of various functional groups into peptides, which is essential for the development of therapeutics and bioconjugates.

In addition to its applications in peptide synthesis, Na-Fmoc-Ne-Boc-Ne-Methyl-D-lysine is also utilized in the study of protein interactions and the design of novel biomolecules. Its ability to provide a stable platform for the attachment of other chemical entities makes it a valuable tool in medicinal chemistry and biochemistry. Researchers appreciate its compatibility with various coupling reagents and its ease of use in complex synthesis protocols, which can significantly streamline the development of new compounds.

Synonyms
Fmoc-D-Lys(Boc,Me)-OH
CAS Number
2044709-77-3
Purity
≥ 99.7% (Chiral HPLC)
Molecular Formula
C27H34N2O6
Molecular Weight
482.6
MDL Number
MFCD15141998
Melting Point
123 - 125 °C
Appearance
White crystalline powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
Fmoc-D-Lys(Boc,Me)-OH
CAS Number
2044709-77-3
Purity
≥ 99.7% (Chiral HPLC)
Molecular Formula
C27H34N2O6
Molecular Weight
482.6
MDL Number
MFCD15141998
Melting Point
123 - 125 °C
Appearance
White crystalline powder
Conditions
Store at 2 - 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-Boc-Ne-Methyl-D-lysine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create complex structures for drug development and biochemical studies.
  • Drug Development: Its unique protective groups facilitate the design of novel therapeutics, particularly in the field of cancer research, where tailored peptides can target specific pathways.
  • Bioconjugation: The compound is used in bioconjugation processes, enabling the attachment of biomolecules to drugs or imaging agents, enhancing their efficacy and specificity.
  • Protein Engineering: Researchers leverage its properties to modify proteins, improving their stability and activity, which is crucial in developing enzyme-based therapies.
  • Analytical Chemistry: It plays a role in analytical methods, such as mass spectrometry, where it aids in the identification and characterization of complex biological molecules.

Citations