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Catalog Number:
32548
CAS Number:
2022956-38-1
Fmoc-Lys(Boc)-Cys(Psi(Me,Me)pro)-OH
Purity:
≥ 99% (HPLC,TLC)
Synonym(s):
Fmoc-Lys(Boc)-Cys(Y(Me,Me)pro)-OH
Antibiotic
Documents
$164.85 /100MG
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Product Information

Fmoc-Lys(Boc)-Cys(Psi(Me,Me)pro)-OH is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a unique structure that combines the protective Fmoc and Boc groups, making it an ideal choice for researchers focused on solid-phase peptide synthesis. Its ability to introduce cysteine residues with specific modifications enhances the stability and functionality of peptides, which is crucial in the design of therapeutic agents and bioconjugates.

The compound's unique thiazolidine ring structure provides additional stability, making it particularly valuable in the development of cyclic peptides and other complex molecular architectures. Researchers in the fields of medicinal chemistry and biochemistry can leverage this compound to create novel peptides with enhanced bioactivity and selectivity. Its application extends to the synthesis of peptide-based drugs, where precise control over amino acid sequences is essential for achieving desired pharmacological effects.

Synonyms
Fmoc-Lys(Boc)-Cys(Y(Me,Me)pro)-OH
CAS Number
2022956-38-1
Purity
≥ 99% (HPLC,TLC)
Molecular Formula
C32H41N3O7S
Molecular Weight
611.76
MDL Number
MFCD23380106
PubChem ID
139211120
Appearance
White to off-white powder
Conditions
Store at ≤ -10 °C
General Information
Synonyms
Fmoc-Lys(Boc)-Cys(Y(Me,Me)pro)-OH
CAS Number
2022956-38-1
Purity
≥ 99% (HPLC,TLC)
Molecular Formula
C32H41N3O7S
Molecular Weight
611.76
MDL Number
MFCD23380106
PubChem ID
139211120
Appearance
White to off-white powder
Conditions
Store at ≤ -10 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
Yes
DEA-regulated
No
Warnings
-
Applications

Fmoc-Lys(Boc)-Cys(Psi(Me,Me)pro)-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the development of biologically active compounds. Its protective groups allow for selective reactions, enhancing the efficiency of peptide assembly.
  • Drug Development: In pharmaceutical research, it is used to create peptide-based drugs. Its unique structure can lead to the discovery of novel therapeutics with improved efficacy and reduced side effects.
  • Bioconjugation: The compound is valuable in bioconjugation processes, where it can be linked to other biomolecules. This application is crucial in developing targeted drug delivery systems and diagnostic agents.
  • Research in Protein Engineering: It aids in the design of modified proteins with enhanced stability and activity. This is particularly beneficial in biotechnology and enzyme engineering, where tailored proteins are needed.
  • Analytical Chemistry: Fmoc-Lys(Boc)-Cys(Psi(Me,Me)pro)-OH is used in various analytical techniques, including mass spectrometry and chromatography, to study complex biological systems and interactions.

Citations