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Catalog Number:
16788
CAS Number:
959583-60-9
Fmoc-L-2-carbamoilfenilalanina
Purity:
≥ 98 % (HPLC)
Synonym(s):
Ácido Fmoc-(2 S -2-amino-3-(2-carbamoilfenil)propanoico
Documents
$72.31 /100 mg
Tamaño
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Product Information

Fmoc-L-2-carbamoylphenylalanine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its unique structure, characterized by the presence of a carbamoyl group on the phenylalanine side chain, enhances its reactivity and stability, making it an ideal choice for researchers focused on developing complex peptide sequences.

In the pharmaceutical industry, Fmoc-L-2-carbamoylphenylalanine is particularly valuable for creating bioactive peptides that can serve as therapeutic agents. Its application extends to the development of peptide-based drugs, where precise control over the amino acid sequence is crucial for achieving desired biological activity. Additionally, this compound can be employed in the study of protein interactions and enzyme mechanisms, providing insights that are essential for advancing drug discovery and development. Researchers will appreciate its ability to facilitate the synthesis of high-purity peptides, ultimately leading to more effective therapeutic solutions.

Synonyms
Ácido Fmoc-(2 S -2-amino-3-(2-carbamoilfenil)propanoico
CAS Number
959583-60-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C25H22N2O5
Molecular Weight
430.45
MDL Number
MFCD06659143
PubChem ID
53398423
Melting Point
222-228 °C
Appearance
Sólido en polvo blanco
Optical Rotation
[a] D 25 = -60,1 ± 2º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Ácido Fmoc-(2 S -2-amino-3-(2-carbamoilfenil)propanoico
CAS Number
959583-60-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C25H22N2O5
Molecular Weight
430.45
MDL Number
MFCD06659143
PubChem ID
53398423
Melting Point
222-228 °C
Appearance
Sólido en polvo blanco
Optical Rotation
[a] D 25 = -60,1 ± 2º (C=1 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-2-carbamoylphenylalanine 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 (SPPS), allowing for the creation of complex and diverse peptide sequences.
  • Drug Development: Its unique structure makes it valuable in the design of new pharmaceuticals, especially in targeting specific biological pathways, enhancing the efficacy of drug candidates.
  • Bioconjugation: The compound can be used in bioconjugation processes, linking peptides to other molecules like antibodies or drugs, which improves the specificity and effectiveness of therapeutic agents.
  • Research in Cancer Therapy: It is being explored in cancer research for developing targeted therapies, as the compound can be modified to interact with cancer cell receptors, potentially leading to more effective treatments.
  • Protein Engineering: Researchers utilize this compound in protein engineering to create modified proteins with enhanced properties, such as stability and activity, which are crucial for various biotechnological applications.

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