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Catalog Number:
02062
CAS Number:
201531-76-2
Fmoc-S-acetamidomethyl-L-penicillamine
Purity:
≥ 96% (HPLC)
Synonym(s):
Fmoc-L-Pen(Acm)-OH, Fmoc-S-acetamidomethyl-β,β-dimethyl-L-Cys-OH
Documents
$100.05 /250MG
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Product Information

Fmoc-S-acetamidomethyl-L-penicillamine is a versatile compound widely utilized in peptide synthesis and drug development. This protected amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) group, which provides stability during the synthesis process while allowing for easy deprotection when needed. Its unique structure, characterized by the acetamidomethyl and penicillamine moieties, enhances its reactivity and selectivity, making it an excellent choice for researchers focused on developing novel therapeutics.

In practical applications, Fmoc-S-acetamidomethyl-L-penicillamine is particularly valuable in the synthesis of peptides that require specific modifications for enhanced biological activity. Its ability to form stable linkages with other amino acids allows for the creation of complex peptide structures, which are essential in the development of targeted drug delivery systems and biologically active compounds. Researchers in medicinal chemistry and biochemistry will find this compound indispensable for advancing their projects, as it streamlines the synthesis process while ensuring high yields and purity.

Synonyms
Fmoc-L-Pen(Acm)-OH, Fmoc-S-acetamidomethyl-β,β-dimethyl-L-Cys-OH
CAS Number
201531-76-2
Purity
≥ 96% (HPLC)
Molecular Formula
C23H26N2O5S
Molecular Weight
442.5
MDL Number
MFCD00151935
Appearance
White solid
Optical Rotation
[a]D25 = -4 ± 2º (C=1 in MeOH)
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-L-Pen(Acm)-OH, Fmoc-S-acetamidomethyl-β,β-dimethyl-L-Cys-OH
CAS Number
201531-76-2
Purity
≥ 96% (HPLC)
Molecular Formula
C23H26N2O5S
Molecular Weight
442.5
MDL Number
MFCD00151935
Appearance
White solid
Optical Rotation
[a]D25 = -4 ± 2º (C=1 in MeOH)
Conditions
Store at 0-8 °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-acetamidomethyl-L-penicillamine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective reactions without interfering with other functional groups. This is crucial for researchers developing complex peptide-based drugs.
  • Drug Development: It plays a significant role in the pharmaceutical industry for creating novel therapeutics, particularly in targeting specific biological pathways, thereby enhancing drug efficacy and safety.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps in attaching biomolecules to surfaces or other molecules, improving the performance of diagnostic tools and therapeutic agents.
  • Research in Cancer Therapy: Its unique properties make it valuable in developing targeted cancer therapies, allowing researchers to create compounds that can selectively attack cancer cells while sparing healthy tissues.
  • Analytical Chemistry: Fmoc-S-acetamidomethyl-L-penicillamine is utilized in analytical methods for detecting and quantifying specific biomolecules, aiding in the development of sensitive assays for various applications.

Citations