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Catalog Number:
05722
CAS Number:
8 de mayo de 2014
Fmoc-L-homocitrulina
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-L-HomoCit-OH, N α-Fmoc- N ε-carbamoil-L-lisina
Documents
$45.77 /250 mg
Tamaño
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Product Information

Fmoc-L-homocitrulline is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound, characterized by its unique Fmoc (9-fluorenylmethyloxycarbonyl) protecting group, offers enhanced stability and solubility, making it an ideal choice for researchers in the fields of biochemistry and medicinal chemistry. Its structure allows for efficient incorporation into peptides, facilitating the exploration of novel therapeutic agents and bioactive compounds.

In practical applications, Fmoc-L-homocitrulline is particularly valuable in the synthesis of cyclic peptides and peptidomimetics, which are crucial in the development of new pharmaceuticals. Its ability to mimic natural amino acids while providing additional functional groups enhances the potential for creating compounds with improved biological activity. Researchers can leverage this compound to investigate various biological pathways and develop targeted therapies, especially in the fields of oncology and immunology. With its unique properties and broad applicability, Fmoc-L-homocitrulline stands out as a key reagent for advancing peptide-based research.

Synonyms
Fmoc-L-HomoCit-OH, N α-Fmoc- N ε-carbamoil-L-lisina
CAS Number
8 de mayo de 2014
Purity
≥ 98 % (HPLC)
Molecular Formula
C22H25N3O5
Molecular Weight
411.4
MDL Number
MFCD00237387
PubChem ID
69110197
Melting Point
168 - 171 ?C
Appearance
Polvo de color blanco a amarillo pálido
Optical Rotation
[a] 20 D = -14 ± 1 ° (C = 2 en DMF)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-L-HomoCit-OH, N α-Fmoc- N ε-carbamoil-L-lisina
CAS Number
8 de mayo de 2014
Purity
≥ 98 % (HPLC)
Molecular Formula
C22H25N3O5
Molecular Weight
411.4
MDL Number
MFCD00237387
PubChem ID
69110197
Melting Point
168 - 171 ?C
Appearance
Polvo de color blanco a amarillo pálido
Optical Rotation
[a] 20 D = -14 ± 1 ° (C = 2 en DMF)
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-L-homocitrulline is widely utilized in research focused on

  • Peptide Synthesis: This compound is a key building block in the synthesis of peptides, particularly in the development of therapeutic proteins. Its Fmoc protection group allows for efficient coupling reactions, making it ideal for solid-phase peptide synthesis.
  • Drug Development: Researchers use Fmoc-L-homocitrulline to create novel drug candidates targeting various diseases, including cancer and metabolic disorders. Its unique structure can enhance the bioactivity of peptides.
  • Bioconjugation: This chemical is employed in bioconjugation processes, where it helps link peptides to other biomolecules, such as antibodies or enzymes, improving the specificity and efficacy of therapeutic agents.
  • Diagnostic Applications: In the field of diagnostics, it is used to develop peptide-based assays and biosensors, aiding in the detection of specific biomarkers for diseases.
  • Research in Immunology: Fmoc-L-homocitrulline is utilized in immunological studies to create modified peptides that can help in understanding immune responses and developing vaccines.

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