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Catalog Number:
11636
CAS Number:
1926163-02-1
N-(9-Fluorenylmethoxycarbonyl)-N-[1-(4-nitro-1,3-dioxo-indan-2-ylidene)ethyl]-L-lysine
Synonym(s):
Fmoc-L-Lys(Nde)-OH
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$106.96 /250MG
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Product Information

Na-(9-Fluorenylmethoxycarbonyl)-Ne-[1-(4-nitro-1,3-dioxo-indan-2-ylidene)ethyl]-L-lysine is a specialized amino acid derivative that serves as a valuable building block in peptide synthesis and drug development. This compound is particularly notable for its protective group, which facilitates the selective modification of amino acids during chemical reactions, enhancing the efficiency of peptide synthesis. Its unique structure allows for the introduction of complex functionalities, making it an ideal candidate for researchers focused on developing novel therapeutic agents or studying protein interactions.

In addition to its role in peptide synthesis, this compound has potential applications in medicinal chemistry, particularly in the design of inhibitors targeting specific biological pathways. The presence of the nitro-indanone moiety may contribute to its biological activity, providing avenues for further exploration in drug discovery. With its robust properties and versatility, Na-(9-Fluorenylmethoxycarbonyl)-Ne-[1-(4-nitro-1,3-dioxo-indan-2-ylidene)ethyl]-L-lysine is an essential tool for researchers aiming to innovate in the fields of biochemistry and pharmacology.

Synonyms
Fmoc-L-Lys(Nde)-OH
CAS Number
1926163-02-1
Molecular Formula
C32H29N3O8
Molecular Weight
583.6
MDL Number
MFCD02684460
PubChem ID
137795022
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-L-Lys(Nde)-OH
CAS Number
1926163-02-1
Molecular Formula
C32H29N3O8
Molecular Weight
583.6
MDL Number
MFCD02684460
PubChem ID
137795022
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-(9-Fluorenylmethoxycarbonyl)-Ne-[1-(4-nitro-1,3-dioxo-indan-2-ylidene)ethyl]-L-lysine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, helping to enhance the stability and yield of the desired products.
  • Drug Development: Its unique structure allows for the design of novel therapeutic agents, particularly in oncology, by targeting specific cancer pathways.
  • Bioconjugation: It is used in bioconjugation processes to link biomolecules, improving the delivery and efficacy of drugs in targeted therapies.
  • Analytical Chemistry: The compound aids in the development of analytical methods for detecting and quantifying biomolecules, facilitating research in biochemistry and molecular biology.
  • Material Science: Its properties make it suitable for creating advanced materials, such as drug delivery systems and smart polymers, enhancing performance in various applications.

Citations