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Catalog Number:
03770
CAS Number:
159700-51-3
Fmoc- S -3-nitro-2-pyridine-sulfényl-L-cystéine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-L-Cys(Npys)-OH
Documents
$60.00 /100 mg
Taille
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Product Information

Fmoc-S-3-nitro-2-pyridine-sulfenyl-L-cysteine is a specialized amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound is particularly valued for its ability to introduce a nitro group into peptides, enhancing their biological activity and stability. Its unique structure, featuring a fluorenylmethoxycarbonyl (Fmoc) protecting group, allows for selective deprotection during synthesis, making it an essential tool for researchers in the fields of medicinal chemistry and biochemistry.

In practical applications, Fmoc-S-3-nitro-2-pyridine-sulfenyl-L-cysteine is utilized in the development of novel therapeutic agents, particularly in the design of inhibitors targeting specific enzymes or receptors. Its ability to form disulfide bonds also makes it a valuable component in the construction of complex peptide architectures. Researchers appreciate its versatility and effectiveness in enhancing the pharmacological properties of peptides, paving the way for innovative treatments in various diseases.

Synonyms
Fmoc-L-Cys(Npys)-OH
CAS Number
159700-51-3
Purity
≥ 98 % (HPLC)
Molecular Formula
C24H21N2O4S2
Molecular Weight
497.54
MDL Number
MFCD00065638
PubChem ID
129011260
Appearance
Poudre jaune
Optical Rotation
[a] D 25 = -63,5 ± 2 º (C = 1 dans MeOH)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Fmoc-L-Cys(Npys)-OH
CAS Number
159700-51-3
Purity
≥ 98 % (HPLC)
Molecular Formula
C24H21N2O4S2
Molecular Weight
497.54
MDL Number
MFCD00065638
PubChem ID
129011260
Appearance
Poudre jaune
Optical Rotation
[a] D 25 = -63,5 ± 2 º (C = 1 dans MeOH)
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-S-3-nitro-2-pyridine-sulfenyl-L-cysteine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for the selective modification of amino acids. Its stability under various conditions makes it a preferred choice for researchers in organic chemistry.
  • Drug Development: It plays a crucial role in the development of new pharmaceuticals, particularly in creating compounds that target specific biological pathways. The unique properties of this chemical can enhance the efficacy of drug candidates.
  • Bioconjugation: This chemical is used in bioconjugation processes to attach biomolecules to surfaces or other molecules, which is essential in creating targeted drug delivery systems and diagnostic tools.
  • Research in Cancer Therapeutics: Its application in cancer research is notable, as it can be utilized to develop compounds that inhibit tumor growth by targeting specific cellular mechanisms.
  • Analytical Chemistry: Fmoc-S-3-nitro-2-pyridine-sulfenyl-L-cysteine is employed in analytical methods to study protein interactions and modifications, providing valuable insights into protein function and structure.

Citations