N,S-Bis-Fmoc-glutathione is a synthetic derivative of glutathione, a tripeptide composed of glutamate, cysteine, and glycine, known for its role as a crucial antioxidant in biological systems. This compound features two Fmoc (9-fluorenylmethoxycarbonyl) protective groups, which are commonly used in peptide synthesis to protect amino groups during chemical reactions. The presence of these groups enhances the stability and solubility of the molecule, making it useful in various biochemical applications, including peptide synthesis and drug development. N,S-Bis-Fmoc-glutathione retains the thiol group from cysteine, which is essential for its reactivity and potential biological activity. The compound is typically characterized by its ability to undergo deprotection under specific conditions, allowing for the release of the active glutathione structure. Its applications extend to research in biochemistry and medicinal chemistry, particularly in studies involving oxidative stress and cellular defense mechanisms. As with many synthetic compounds, proper handling and storage are essential to maintain its integrity and effectiveness in experimental settings.

N,S-Bis-Fmoc-glutathione

149438-56-2: N,S-Bis-Fmoc-glutathione is a synthetic derivative of glutathione, a tripeptide composed of glutamate, cysteine, and glycine, known for its role as a crucial antioxidant in biological systems. This compound features two Fmoc (9-fluorenylmethoxycarbonyl) protective groups, which are commonly used in peptide synthesis to protect amino groups during chemical reactions. The presence of these groups enhances the stability and solubility of the molecule, making it useful in various biochemical applications, including peptide synthesis and drug development. N,S-Bis-Fmoc-glutathione retains the thiol group from cysteine, which is essential for its reactivity and potential biological activity. The compound is typically characterized by its ability to undergo deprotection under specific conditions, allowing for the release of the active glutathione structure. Its applications extend to research in biochemistry and medicinal chemistry, particularly in studies involving oxidative stress and cellular defense mechanisms. As with many synthetic compounds, proper handling and storage are essential to maintain its integrity and effectiveness in experimental settings.

Very potent inhibitor of mammalian glyoxalase II (Ki = 0.08 µM for glyoxalase II purified from calf liver).

<p>N,S-Bis-Fmoc-Glutathione is a potent inhibitor of glyoxalase II, exhibiting a K i of 0.32 mM [1].</p>

N,S-Bis-Fmoc-Glutathione

<p>Please enquire for more information about N,S-Bis-Fmoc-glutathione Fmoc-Glu(Cys(Fmoc)-Gly-OH)-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

CAS 149438-56-2

N,S-Bis-Fmoc-glutathione

N,S-Bis-Fmoc-glutathione

Ref: 01-4026654

N,S-Bis-Fmoc-Glutathione

Ref: TM-T80098

N,S-Bis-Fmoc-glutathione Fmoc-Glu(Cys(Fmoc)-Gly-OH)-OH

Ref: 3D-FB111325