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Catalog Number:
12711
CAS Number:
150308-80-8
Fmoc-( S )-4-metoxibencil selenocisteína
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-L-Sec(pMeOBzl)-OH
Documents
$105.36 /25 mg
Tamaño
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Product Information

Fmoc-(S)-4-methoxybenzyl selenocysteine is a specialized amino acid derivative that plays a crucial role in peptide synthesis and bioconjugation applications. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which allows for selective deprotection during synthesis, making it an invaluable tool for researchers in the fields of medicinal chemistry and biochemistry. Its unique selenocysteine moiety introduces selenium into peptides, which can enhance biological activity and stability, offering potential advantages over traditional sulfur-containing amino acids.

Researchers utilize Fmoc-(S)-4-methoxybenzyl selenocysteine in the development of novel therapeutics, particularly in the design of selenoproteins and selenium-based drugs. Its ability to facilitate the incorporation of selenium into peptide sequences opens new avenues for studying the role of selenium in biological systems and its implications in disease prevention. This compound is particularly relevant for those exploring antioxidant properties and the development of targeted therapies, making it a valuable addition to any laboratory focused on innovative chemical research.

Synonyms
Fmoc-L-Sec(pMeOBzl)-OH
CAS Number
150308-80-8
Purity
≥ 98 % (HPLC)
Molecular Formula
C26H25NO5Se
Molecular Weight
510.4
MDL Number
MFCD03788170
PubChem ID
85129961
Melting Point
138 - 141 °C
Appearance
Polvo blanco o blanquecino
Optical Rotation
[a]20D = -36 ± 1 ° (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-L-Sec(pMeOBzl)-OH
CAS Number
150308-80-8
Purity
≥ 98 % (HPLC)
Molecular Formula
C26H25NO5Se
Molecular Weight
510.4
MDL Number
MFCD03788170
PubChem ID
85129961
Melting Point
138 - 141 °C
Appearance
Polvo blanco o blanquecino
Optical Rotation
[a]20D = -36 ± 1 ° (C=1 en DMF)
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-(S)-4-methoxybenzyl selenocysteine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly those that require selenium for enhanced biological activity.
  • Antioxidant Research: Its unique selenium-containing structure makes it a key player in studies investigating antioxidant properties, potentially leading to new therapeutic agents.
  • Drug Development: The compound is explored in the pharmaceutical industry for developing novel drugs, especially in targeting diseases where selenium plays a crucial role in metabolism.
  • Bioconjugation: It is used in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, enhancing specificity in drug delivery systems.
  • Protein Engineering: This chemical aids in the design of proteins with improved stability and functionality, particularly in biotechnological applications.

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