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Catalog Number:
29640
CAS Number:
1013096-03-1
Fmoc- N -metil-S- terc -butiltio-L-cisteína
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc -N -Me-L-Cys(StBu)-OH
Documents
$115.00 /25 mg
Tamaño
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Product Information

Fmoc-N-methyl-S-tert-butylthio-L-cysteine is a valuable compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of the amine group during solid-phase peptide synthesis. Its unique structure, which includes a methyl and a tert-butylthio group, enhances its stability and solubility, making it an ideal choice for researchers looking to develop complex peptides with improved bioactivity.

In the pharmaceutical industry, Fmoc-N-methyl-S-tert-butylthio-L-cysteine is particularly beneficial for synthesizing peptide-based therapeutics, where precise control over amino acid sequences is crucial. Its application extends to the development of novel drug candidates, especially in the field of cancer research, where peptides are being explored for targeted therapies. By incorporating this compound into their workflows, researchers can achieve higher yields and purities in their peptide synthesis, ultimately accelerating the discovery of new therapeutic agents.

Synonyms
Fmoc -N -Me-L-Cys(StBu)-OH
CAS Number
1013096-03-1
Purity
≥ 98 % (HPLC)
Molecular Formula
C23H27NO4S2
Molecular Weight
445.59
MDL Number
MFCD24849705
PubChem ID
117736054
Melting Point
101 - 112 °C (Literatura)
Appearance
Sólido blanco
Optical Rotation
[a] D 20 = -11,6 ± 2 º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc -N -Me-L-Cys(StBu)-OH
CAS Number
1013096-03-1
Purity
≥ 98 % (HPLC)
Molecular Formula
C23H27NO4S2
Molecular Weight
445.59
MDL Number
MFCD24849705
PubChem ID
117736054
Melting Point
101 - 112 °C (Literatura)
Appearance
Sólido blanco
Optical Rotation
[a] D 20 = -11,6 ± 2 º (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-N-methyl-S-tert-butylthio-L-cysteine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a building block in the synthesis of peptides, particularly in solid-phase synthesis, allowing for the incorporation of unique functionalities that enhance the properties of the resulting peptides.
  • Drug Development: It plays a crucial role in the development of peptide-based therapeutics, providing a means to create more effective drugs with improved stability and bioavailability.
  • Bioconjugation: The compound is used in bioconjugation techniques, facilitating the attachment of peptides to other biomolecules, which is essential in creating targeted drug delivery systems.
  • Research in Protein Engineering: It aids researchers in modifying cysteine residues in proteins, enabling the study of protein structure and function, as well as the development of novel protein-based materials.
  • Analytical Chemistry: This chemical is utilized in analytical methods for detecting and quantifying thiol-containing compounds, which is important in various biochemical assays and studies.

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