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Catalog Number:
03759
CAS Number:
214852-56-9
Fmoc-3-(2'-quinoil)-L-alanina
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-L-Ala(2'-quinolil)-OH, Ácido Fmoc-( S )-2-amino-3-quinolin-2-il-propiónico
Documents
$201.20 /25 mg
Tamaño
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Product Information

Fmoc-3-(2'-quinoyl)-L-alanine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which allows for selective deprotection during the synthesis process, making it an essential tool for researchers in the field of medicinal chemistry. Its quinoline moiety enhances the compound's biological activity, providing potential applications in the development of novel therapeutics, particularly in targeting specific receptors or enzymes.

Researchers appreciate the stability and ease of handling of Fmoc-3-(2'-quinoyl)-L-alanine, which facilitates its incorporation into complex peptide sequences. This compound is particularly valuable in the synthesis of bioactive peptides and can be employed in various applications, including drug discovery, cancer research, and the development of targeted therapies. Its unique structure not only contributes to its efficacy but also offers advantages over similar compounds, making it a preferred choice for professionals seeking reliable and effective building blocks in their research.

Synonyms
Fmoc-L-Ala(2'-quinolil)-OH, Ácido Fmoc-( S )-2-amino-3-quinolin-2-il-propiónico
CAS Number
214852-56-9
Purity
≥ 99 % (HPLC)
Molecular Formula
C27H22N2O4
Molecular Weight
438.5
MDL Number
MFCD01318745
PubChem ID
4384852
Appearance
Polvo de color blanco o blanquecino a amarillo pálido.
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-L-Ala(2'-quinolil)-OH, Ácido Fmoc-( S )-2-amino-3-quinolin-2-il-propiónico
CAS Number
214852-56-9
Purity
≥ 99 % (HPLC)
Molecular Formula
C27H22N2O4
Molecular Weight
438.5
MDL Number
MFCD01318745
PubChem ID
4384852
Appearance
Polvo de color blanco o blanquecino a amarillo pálido.
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-3-(2'-quinoyl)-L-alanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for the selective modification of amino acids without affecting others. Its stability under various conditions makes it ideal for complex peptide assembly.
  • Drug Development: In pharmaceutical research, it is used to create novel drug candidates, particularly those targeting specific receptors. The quinoline moiety can enhance bioactivity and selectivity, which is crucial in developing effective medications.
  • Bioconjugation: This chemical is employed in bioconjugation processes, linking biomolecules such as proteins and antibodies to therapeutic agents. This application is vital in creating targeted therapies for diseases like cancer.
  • Fluorescent Probes: Its unique structure allows for the development of fluorescent probes used in biological imaging. This application aids researchers in visualizing cellular processes and tracking drug delivery in real-time.
  • Research in Neuroscience: The compound is explored in neuroscience for its potential neuroprotective effects. Studies suggest that derivatives may help in understanding neurodegenerative diseases and developing treatments.

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