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Catalog Number:
35205
CAS Number:
1349807-46-0
Fmoc- S -trityl- N -méthyl-D-cystéine
Purity:
≥ 99,5 % (HPLC chirale)
Synonym(s):
Fmoc- N -Me-D-Cys(trt)-OH
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$240.00 /250 mg
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Product Information

Fmoc-S-trityl-N-methyl-D-cysteine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (9-fluorenylmethyloxycarbonyl) group, which facilitates the selective deprotection of the amino group during solid-phase peptide synthesis. Its unique trityl (triphenylmethyl) protecting group enhances stability and solubility, making it an excellent choice for complex peptide sequences. Researchers and industry professionals appreciate its role in synthesizing bioactive peptides, particularly in the development of therapeutics targeting various diseases.

The compound's ability to provide a stable and easily removable protecting group allows for efficient synthesis and purification processes, which are crucial in pharmaceutical applications. Fmoc-S-trityl-N-methyl-D-cysteine is particularly beneficial in the production of cyclic peptides and peptidomimetics, offering potential advantages over similar compounds due to its enhanced stability and ease of handling. This makes it an essential tool for chemists and researchers aiming to innovate in the fields of drug discovery and development.

Synonyms
Fmoc- N -Me-D-Cys(trt)-OH
CAS Number
1349807-46-0
Purity
≥ 99,5 % (HPLC chirale)
Molecular Formula
C 38 H 33 NON 4 S
Molecular Weight
599.74
MDL Number
MFCD20441470
PubChem ID
53396279
Appearance
Solide blanc
Optical Rotation
[a] D 20 = 28 ± 1 ° (C = 1 en DCM)
Conditions
Magasin chez RT
General Information
Synonyms
Fmoc- N -Me-D-Cys(trt)-OH
CAS Number
1349807-46-0
Purity
≥ 99,5 % (HPLC chirale)
Molecular Formula
C 38 H 33 NON 4 S
Molecular Weight
599.74
MDL Number
MFCD20441470
PubChem ID
53396279
Appearance
Solide blanc
Optical Rotation
[a] D 20 = 28 ± 1 ° (C = 1 en DCM)
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-S-trityl-N-methyl-D-cysteine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis. Its protective groups allow for selective reactions, enhancing yield and purity.
  • Drug Development: In pharmaceutical research, it is used to create peptide-based drugs, especially those targeting specific receptors. Its unique structure can improve the stability and efficacy of drug candidates.
  • Bioconjugation: The compound is valuable in bioconjugation processes, where it helps attach peptides to other biomolecules, such as antibodies or nanoparticles, facilitating targeted drug delivery systems.
  • Research in Proteomics: It plays a significant role in proteomics studies, aiding in the identification and characterization of proteins through mass spectrometry, thanks to its ability to form stable adducts.
  • Antioxidant Research: The compound is also explored for its potential antioxidant properties, contributing to studies aimed at developing new therapies for oxidative stress-related diseases.

Citations