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R-L-glyceroylglutathione is a complex organic compound that plays a significant role in cellular metabolism and detoxification processes. It is a conjugate of glycerol and glutathione, which is a tripeptide composed of glutamate, cysteine, and glycine. R-L-glyceroylglutathione is involved in the metabolism of fatty acids and the detoxification of various xenobiotics, including drugs and environmental toxins. R-L-glyceroylglutathione is particularly important for maintaining cellular redox balance and protecting cells from oxidative stress. It is also implicated in the regulation of cellular signaling pathways and the maintenance of cellular homeostasis. The compound's specific role in these processes highlights its importance in maintaining overall health and functioning of various biological systems.

3878-83-9

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3878-83-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3878-83-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,7 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3878-83:
(6*3)+(5*8)+(4*7)+(3*8)+(2*8)+(1*3)=129
129 % 10 = 9
So 3878-83-9 is a valid CAS Registry Number.

3878-83-9Downstream Products

3878-83-9Relevant academic research and scientific papers

S-2-Hydroxyacylglutathione-Derivatives: Enzymatic Preparation, Purification and Characterisation

Clelland, James D.,Thornalley, Paul J.

, p. 3009 - 3016 (2007/10/02)

S-2-Hydroxyacylglutathione derivatives have been prepared by enzymatic synthesis from α-oxoaldehydes and reduced glutathione in the presence of glyoxalase I.S-D-Lactoylglutathione, S-D-mandelylglutathione, S-glycolylglutathione and S-L-glyceroylglutathione were prepared from methylglyoxal, phenylglyoxal, glyoxal and hydroxypyruvaldehyde, respectively.They were purified by ion exchange chromatography on Dowex 1 on a gram scale.Analytical data and re-evaluated extinction coefficients for these compounds are presented.The method described provides a reliable, large-scale procedure for the preparation and purification of S-acylglutathiones of increasing biological and pharmacological interest.

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