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Catalog Number:
15719
CAS Number:
511272-45-0
Fmoc-(R-3-amino-3-(2-furyl)propionic acid
Synonym(s):
Fmoc-L-β-Ala-(2-furyl)-OH
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Product Information

Fmoc-(R)-3-amino-3-(2-furyl)propionic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amine functionalities during the synthesis of complex peptides. Its unique structure, which includes a furan ring, enhances its reactivity and compatibility with various coupling reagents, making it an ideal choice for researchers focused on developing novel therapeutic peptides.

In addition to its role in peptide synthesis, Fmoc-(R)-3-amino-3-(2-furyl)propionic acid has shown potential in the design of bioactive compounds, particularly in the fields of drug discovery and development. Its ability to facilitate the introduction of chirality into peptide sequences allows for the creation of more effective and selective drug candidates. Researchers can leverage this compound to explore new avenues in pharmacology, particularly in the development of targeted therapies for various diseases.

Synonyms
Fmoc-L-β-Ala-(2-furyl)-OH
CAS Number
511272-45-0
Molecular Formula
C22H19NO5
Molecular Weight
377.4
MDL Number
MFCD04117844
PubChem ID
24902259
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-L-β-Ala-(2-furyl)-OH
CAS Number
511272-45-0
Molecular Formula
C22H19NO5
Molecular Weight
377.4
MDL Number
MFCD04117844
PubChem ID
24902259
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

Fmoc-(R)-3-amino-3-(2-furyl)propionic acid is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a crucial building block in the synthesis of peptides, particularly in solid-phase peptide synthesis (SPPS), allowing researchers to create complex peptide sequences efficiently.
  • Drug Development: Its unique structure makes it valuable in the pharmaceutical industry for developing novel drugs that target specific biological pathways, enhancing therapeutic efficacy.
  • Bioconjugation: The compound can be used to modify biomolecules, facilitating the attachment of drugs or imaging agents to proteins or antibodies, which is essential in targeted therapy and diagnostics.
  • Research in Neuroscience: Due to its structural similarity to neurotransmitters, it is employed in studies investigating neuronal signaling and the development of neuroprotective agents.
  • Material Science: This chemical is also explored in the development of functional materials, such as hydrogels, which can be used in drug delivery systems or tissue engineering applications.

Citations