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Catalog Number:
03760
CAS Number:
214852-58-1
Fmoc-3-(2'-quinolyl)-D-alanine
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-D-Ala(2'-quinolyl)-OH
Documents
$231.40 /100 mg
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Product Information

Fmoc-3-(2'-quinolyl)-D-alanine 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 quinoline moiety enhances its potential as a building block for bioactive peptides, making it particularly valuable in medicinal chemistry and pharmaceutical research. Researchers appreciate its stability and compatibility with various coupling reagents, which streamline the synthesis process and improve yields.

In addition to its role in peptide synthesis, Fmoc-3-(2'-quinolyl)-D-alanine has shown promise in the development of novel therapeutic agents, particularly in targeting specific biological pathways. Its structural characteristics allow for the design of compounds with enhanced bioactivity and selectivity. This compound is ideal for researchers focused on developing new drugs or studying peptide interactions, as it provides a reliable and efficient means of constructing complex peptide structures.

Synonyms
Fmoc-D-Ala(2'-quinolyl)-OH
CAS Number
214852-58-1
Purity
≥ 99 % (HPLC)
Molecular Formula
C27H22N2O4
Molecular Weight
438.5
MDL Number
MFCD01318746
PubChem ID
4384852
Melting Point
174 - 185 °C (déc.)
Appearance
Poudre blanche ou blanc cassé
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Fmoc-D-Ala(2'-quinolyl)-OH
CAS Number
214852-58-1
Purity
≥ 99 % (HPLC)
Molecular Formula
C27H22N2O4
Molecular Weight
438.5
MDL Number
MFCD01318746
PubChem ID
4384852
Melting Point
174 - 185 °C (déc.)
Appearance
Poudre blanche ou blanc cassé
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-3-(2'-quinolyl)-D-alanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: Its unique structure enhances the bioactivity of peptide-based drugs, making it valuable in the pharmaceutical industry for developing new therapeutics.
  • Bioconjugation: The compound can be used to create bioconjugates, linking peptides to other biomolecules, which is crucial in the development of targeted drug delivery systems.
  • Fluorescent Probes: Due to its quinoline moiety, it can be utilized in the design of fluorescent probes for biological imaging, aiding researchers in visualizing cellular processes.
  • Research on Protein Interactions: It is beneficial in studying protein-ligand interactions, providing insights into molecular mechanisms that can lead to advancements in biotechnology and molecular biology.

Citations