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Catalog Number:
14453
CAS Number:
917099-01-5
Ácido R -Fmoc-4-amino-5-(3-indolil)pentanoico
Purity:
≥ 99,5 % (HPLC quiral)
Documents
$93.14 /100 mg
Tamaño
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Product Information

(R)-Fmoc-4-amino-5-(3-indolyl)pentanoic acid 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, incorporating an indole moiety, enhances its bioactivity and makes it a valuable building block in medicinal chemistry, particularly in the design of bioactive peptides and pharmaceuticals targeting various biological pathways.

Researchers and industry professionals appreciate (R)-Fmoc-4-amino-5-(3-indolyl)pentanoic acid for its ability to facilitate the synthesis of complex peptide structures with improved stability and solubility. Its application extends to the development of therapeutic agents, including those targeting cancer and neurodegenerative diseases. The compound's favorable properties, such as its compatibility with various coupling reagents and its ease of deprotection, make it an ideal choice for both academic research and industrial applications in peptide synthesis.

CAS Number
917099-01-5
Purity
≥ 99,5 % (HPLC quiral)
Molecular Formula
C28H26N2O4
Molecular Weight
454.52
MDL Number
MFCD06410971
PubChem ID
4712551
Appearance
Sólido de color blanco a blanquecino
Optical Rotation
[a] D 20 = -14 ± 2 º (C=1 en MeOH)
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
917099-01-5
Purity
≥ 99,5 % (HPLC quiral)
Molecular Formula
C28H26N2O4
Molecular Weight
454.52
MDL Number
MFCD06410971
PubChem ID
4712551
Appearance
Sólido de color blanco a blanquecino
Optical Rotation
[a] D 20 = -14 ± 2 º (C=1 en MeOH)
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

(R)-Fmoc-4-amino-5-(3-indolyl)pentanoic acid 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, allowing for the efficient assembly of complex peptide structures.
  • Drug Development: Its unique structure makes it valuable in the pharmaceutical industry for developing new drug candidates, especially those targeting specific biological pathways involving indole derivatives.
  • Bioconjugation: The compound can be used in bioconjugation processes, enabling the attachment of biomolecules to drugs or imaging agents, enhancing their efficacy and specificity.
  • Research in Neuroscience: Due to its indole component, it is explored in neuroscience research for potential applications in developing treatments for mood disorders and neurodegenerative diseases.
  • Protein Engineering: The compound is beneficial in protein engineering, where it can be incorporated into proteins to study structure-function relationships and improve protein stability.

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