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Catalog Number:
32801
CAS Number:
149438-56-2
N,S-Bis-Fmoc-glutathione
Synonym(s):
Fmoc-Glu(Cys(Fmoc)-Gly-OH)-OH
Documents
$113.87 /100MG
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Product Information

N,S-Bis-Fmoc-glutathione is a sophisticated derivative of glutathione, designed for advanced applications in peptide synthesis and drug development. This compound features a unique structure that enhances its stability and solubility, making it an ideal choice for researchers focused on bioconjugation and the development of targeted therapies. Its protective Fmoc (fluorenylmethyloxycarbonyl) groups allow for selective deprotection, facilitating the synthesis of complex peptides and proteins with high precision.

In the pharmaceutical industry, N,S-Bis-Fmoc-glutathione is particularly valuable for its role in the synthesis of peptide-based drugs and as a building block in the creation of novel therapeutics. Its ability to improve the bioavailability of active pharmaceutical ingredients (APIs) makes it a preferred choice among researchers and formulators. Additionally, its applications extend to the fields of diagnostics and biomaterials, where it can be utilized in the development of biosensors and drug delivery systems. With its unique properties and versatile applications, N,S-Bis-Fmoc-glutathione stands out as a key compound for professionals seeking innovative solutions in chemical research and development.

Synonyms
Fmoc-Glu(Cys(Fmoc)-Gly-OH)-OH
CAS Number
149438-56-2
Molecular Formula
C40H37N3O10S
Molecular Weight
751.81
MDL Number
MFCD00798635
PubChem ID
171036511
Conditions
Store at ≤ -10 °C
General Information
Synonyms
Fmoc-Glu(Cys(Fmoc)-Gly-OH)-OH
CAS Number
149438-56-2
Molecular Formula
C40H37N3O10S
Molecular Weight
751.81
MDL Number
MFCD00798635
PubChem ID
171036511
Conditions
Store at ≤ -10 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

N,S-Bis-Fmoc-glutathione 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 while preventing unwanted reactions.
  • Drug Development: It plays a crucial role in the development of new pharmaceuticals, particularly in creating compounds that can effectively target specific biological pathways.
  • Bioconjugation: Researchers use it to facilitate the attachment of biomolecules to various surfaces, enhancing the effectiveness of drug delivery systems and diagnostic tools.
  • Antioxidant Research: Its properties allow scientists to study the mechanisms of oxidative stress and develop potential therapeutic strategies for diseases related to oxidative damage.
  • Analytical Chemistry: The compound is employed in various analytical techniques, improving the sensitivity and selectivity of assays used in biochemical research.

Citations