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Catalog Number:
33685
Fmoc-(2S,3S-3-amino-2-hydroxy-3-(3,4-dimethoxyphenyl)-propionic acid
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$100.05 /25MG
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Product Information

Fmoc-(2S,3S)-3-amino-2-hydroxy-3-(3,4-dimethoxyphenyl)propionic acid is a versatile amino acid derivative widely utilized in peptide synthesis and medicinal chemistry. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which facilitates the selective protection of amino groups during the synthesis of peptides. Its structural characteristics make it an excellent choice for researchers focusing on the development of bioactive peptides and pharmaceuticals. The presence of the 3,4-dimethoxyphenyl group enhances its stability and solubility, making it suitable for various applications in drug formulation and delivery systems.

In addition to its role in peptide synthesis, this compound has shown potential in the development of novel therapeutic agents, particularly in the fields of cancer research and neuropharmacology. Its ability to modulate biological activity makes it a valuable tool for researchers aiming to explore new pathways in drug discovery. With its favorable properties and applications, Fmoc-(2S,3S)-3-amino-2-hydroxy-3-(3,4-dimethoxyphenyl)propionic acid stands out as a crucial component for advancing research in medicinal chemistry and related fields.

Molecular Formula
C26H25NO7
Molecular Weight
463.48
MDL Number
MFCD07363687
Conditions
Store at 2 - 8 °C
General Information
Molecular Formula
C26H25NO7
Molecular Weight
463.48
MDL Number
MFCD07363687
Conditions
Store at 2 - 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-(2S,3S)-3-amino-2-hydroxy-3-(3,4-dimethoxyphenyl)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in solid-phase peptide synthesis, allowing for the selective modification of amino acids while preventing unwanted reactions.
  • Drug Development: Its unique structure aids in the design of novel pharmaceuticals, particularly in creating compounds with enhanced bioactivity and specificity for target receptors.
  • Bioconjugation: It is employed in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in developing diagnostic tools and therapeutic agents.
  • Research in Neuroscience: The compound's analogs are studied for their potential neuroprotective effects, contributing to the understanding of neurodegenerative diseases and the development of new treatments.
  • Material Science: Its properties make it valuable in creating functionalized materials, such as hydrogels, which can be used in drug delivery systems and tissue engineering applications.

Citations