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Catalog Number:
15371
CAS Number:
270065-69-5
Fmoc-(4-pyridyl)-L-ॆ-homoalanine
Purity:
≥ 97% (HPLC)
Synonym(s):
Fmoc-L-β-HomoAla(4-pyridyl)-OH, Fmoc-(S)-3-amino-4-(4-pyridyl)butyric acid
Documents
$120.00 /25MG
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Product Information

Fmoc-(4-pyridyl)-L-b-homoalanine 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 pyridyl side chain enhances the compound's ability to participate in various chemical reactions, making it an attractive choice for researchers focused on developing novel therapeutic agents.

In the pharmaceutical industry, Fmoc-(4-pyridyl)-L-b-homoalanine is particularly valuable for the synthesis of bioactive peptides, which can serve as potential drugs or research tools. Its stability and compatibility with standard coupling reagents allow for efficient incorporation into peptide sequences, facilitating the exploration of structure-activity relationships. Additionally, the compound's distinct properties may lead to improved binding affinities and selectivity in biological applications, making it a preferred choice for professionals engaged in medicinal chemistry and peptide research.

Synonyms
Fmoc-L-β-HomoAla(4-pyridyl)-OH, Fmoc-(S)-3-amino-4-(4-pyridyl)butyric acid
CAS Number
270065-69-5
Purity
≥ 97% (HPLC)
Molecular Formula
C24H22N2O4
Molecular Weight
402.45
MDL Number
MFCD01861059
PubChem ID
53397941
Melting Point
172 - 178 ºC
Appearance
White or yellowish powder
Optical Rotation
[a]D25 = -25 to -20 º (C=1 in DMF)
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-L-β-HomoAla(4-pyridyl)-OH, Fmoc-(S)-3-amino-4-(4-pyridyl)butyric acid
CAS Number
270065-69-5
Purity
≥ 97% (HPLC)
Molecular Formula
C24H22N2O4
Molecular Weight
402.45
MDL Number
MFCD01861059
PubChem ID
53397941
Melting Point
172 - 178 ºC
Appearance
White or yellowish powder
Optical Rotation
[a]D25 = -25 to -20 º (C=1 in DMF)
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-(4-pyridyl)-L-b-homoalanine 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, enhancing the efficiency and yield of the process.
  • Drug Development: Its unique structure allows for the design of novel therapeutic agents, especially in the development of drugs targeting specific biological pathways, making it valuable in pharmaceutical research.
  • Bioconjugation: The compound is used in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, which is essential in creating targeted drug delivery systems.
  • Research in Cancer Therapeutics: It has applications in cancer research, where it can be incorporated into compounds that selectively target cancer cells, potentially improving treatment efficacy.
  • Material Science: The chemical is also explored in the development of functional materials, such as sensors and catalysts, due to its ability to interact with various substrates.

Citations