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Catalog Number:
33682
Ácido Fmoc-(2 R ,3 R -3-amino-2-hidroxi-3-(2,3-dimetoxifenil)propiónico
Documents
$100.05 /25 mg
Tamaño
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Product Information

Fmoc-(2R,3R)-3-amino-2-hydroxy-3-(2,3-dimethoxyphenyl)propionic acid is a versatile compound widely utilized in peptide synthesis and medicinal chemistry. This amino acid derivative, characterized by its Fmoc (9-fluorenylmethoxycarbonyl) protecting group, facilitates the efficient assembly of peptides through solid-phase synthesis. Its unique structure, featuring a hydroxyl group and a dimethoxyphenyl side chain, enhances its solubility and reactivity, making it an ideal choice for researchers focused on developing novel therapeutic peptides.

In addition to its role in peptide synthesis, this compound has shown potential in the development of bioactive molecules, particularly in the fields of drug discovery and development. Its ability to form stable interactions with biological targets allows for the exploration of new pharmacological pathways. Researchers can leverage this compound to create tailored peptides that can serve as inhibitors or modulators in various biological processes, thus expanding the horizons of therapeutic applications. With its favorable properties and practical uses, Fmoc-(2R,3R)-3-amino-2-hydroxy-3-(2,3-dimethoxyphenyl)propionic acid stands out as a valuable tool for professionals in the pharmaceutical and biotechnology sectors.

Molecular Formula
C26H25Nº7
Molecular Weight
463.48
MDL Number
MFCD07363684
Conditions
Conservar entre 2 y 8 °C.
General Information
Molecular Formula
C26H25Nº7
Molecular Weight
463.48
MDL Number
MFCD07363684
Conditions
Conservar entre 2 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-(2R,3R)-3-amino-2-hydroxy-3-(2,3-dimethoxyphenyl)propionic 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 (SPPS), allowing for the creation of complex peptide structures with high purity.
  • Drug Development: Its unique structure can be leveraged in the design of novel pharmaceuticals, especially in targeting specific biological pathways, enhancing the efficacy of drug candidates.
  • Bioconjugation: The compound can be used to attach biomolecules to surfaces or other molecules, facilitating the development of targeted drug delivery systems and diagnostic tools.
  • Research in Neuroscience: It may play a role in the study of neuroactive peptides, contributing to the understanding of neurological disorders and potential therapeutic approaches.
  • Material Science: This chemical can be incorporated into polymers or materials to impart specific properties, such as increased biocompatibility or enhanced mechanical strength, useful in biomedical applications.

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