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Deamino-Glutathion
Nombre químico: (R)-5-((1-((carboxymethyl)amino)-3-mercapto-1-oxopropan-2-yl)amino)-5-oxopentanoic acid
- Nº Artículo:LS-4675
- Nº CAS:117974-05-7
- Fórmula:C10H16N2O6S
- Storage temperature:-20°C
- Masa molecular:292,31 g/mol
from 500,00 €
references
Quantifying Escherichia coli glutaredoxin-3 substrate specificity using ligand-induced stability; T. H. Elgán, K. D. Berndt; J Biol Chem. 2008; 283(47): 32839-47. https://doi.org/10.1074/jbc.m804019200
Kinetic studies on rat liver microsomal glutathione transferase: consequences of activation; C. Andersson, F. Piemonte, E. Mosialou, R. Weinander, T.-H. Sun, G. Lundqvist, A. E. P. Adang, R. Morgenstern; Biochim. Biophys. Acta 1995; 1247(2): 277-283. https://doi.org/10.1016/0167-4838(94)00239-D
Identification of N-acetylcysteine as a new substrate for rat liver microsomal glutathione transferase. A study of thiol ligands; R. Weinander, C. Anderson, R. Morgenstern; J. Biol. Chem. 1994; 269(1): 71-76. https://doi.org/10.1016/S0021-9258(17)42315-5
Interaction of rat glutathione S-transferases 7-7 and 8-8 with ã-glutamyl- or glycyl-modified glutathione analogues; A. E. P. Adang, D. J. Meyer, J. Brussee, A. Van der Gen, B. Ketterer, G. J. Mulder; Biochem J 1989; 264(3): 759-764. https://doi.org/10.1042/bj2640759
Substrate specificity of rat liver glutathione S-transferase isoenzymes for a series of glutathione analogues, modified at the gamma-glutamyl moiety; A. E. P. Adang, J. Brussee, D. J. Meyer, B. Coles, B. Ketterer, A. Van der Gen, G. J. Mulder; Biochem J 1988; 255(2): 721-724. https://pubmed.ncbi.nlm.nih.gov/2904809/
Synthesis and nucleophilic reactivity of a series of glutathione analogues, modified at the gamma-glutamyl moiety; A. E. P. Adang, A. J. Duindam, J. Brussee, G. J. Mulder, A. Van der Gen; Biochem J 1988; 255(2): 715-720. https://pubmed.ncbi.nlm.nih.gov/2904808/
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Prices and product availability are subject to change and require reconfirmation. Please contact us for further information.
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