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Catalog Number:
37436
CAS Number:
205182-52-1
Fmoc-L-HomoTyr(Me)-OH
Purity:
≥ 99.5% (ee, Chiral HPLC)
Synonym(s):
Fmoc-L-O-Methyl-Homotyrosine, Fmoc-L-HomoPhe(4-OMe)-OH
Documents
$230.00 /250MG
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Product Information

Fmoc-L-HomoTyr(Me)-OH 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 solid-phase peptide synthesis. Its unique structure, characterized by the presence of a methoxy group on the aromatic ring, enhances its solubility and stability, making it an ideal choice for researchers focusing on complex peptide sequences.

In practical applications, Fmoc-L-HomoTyr(Me)-OH is particularly valuable in the synthesis of bioactive peptides and pharmaceuticals, where precise control over amino acid sequences is crucial. Its ability to facilitate the incorporation of non-standard amino acids into peptides opens up new avenues for the development of innovative therapeutics. Researchers in medicinal chemistry and biochemistry will find this compound indispensable for advancing their projects, especially in the design of peptide-based drugs with improved efficacy and specificity.

Synonyms
Fmoc-L-O-Methyl-Homotyrosine, Fmoc-L-HomoPhe(4-OMe)-OH
CAS Number
205182-52-1
Purity
≥ 99.5% (ee, Chiral HPLC)
Molecular Formula
C26H25NO5
Molecular Weight
431.23
PubChem ID
53421128
Appearance
White powder
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-L-O-Methyl-Homotyrosine, Fmoc-L-HomoPhe(4-OMe)-OH
CAS Number
205182-52-1
Purity
≥ 99.5% (ee, Chiral HPLC)
Molecular Formula
C26H25NO5
Molecular Weight
431.23
PubChem ID
53421128
Appearance
White powder
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-L-HomoTyr(Me)-OH 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 without interfering with other functional groups.
  • Drug Development: Its role in the synthesis of peptide-based drugs enhances the stability and bioavailability of therapeutic agents, making it valuable in pharmaceutical research.
  • Bioconjugation: The chemical is used to create conjugates with biomolecules, facilitating targeted drug delivery systems in cancer therapy and other medical applications.
  • Research in Neuroscience: It is employed in the synthesis of neuropeptides, aiding studies on neurotransmitter functions and potential treatments for neurological disorders.
  • Material Science: The compound can be utilized in the development of novel materials with specific properties, such as hydrophobicity or biocompatibility, for various industrial applications.

Citations