CAS 284665-11-8
:N-(9-fluorenylmethoxycarbonyl)glycine-2,2-D2
Description:
N-(9-fluorenylmethoxycarbonyl)glycine-2,2-D2, commonly referred to as Fmoc-Gly-D2, is a derivative of glycine where the amino group is protected by the 9-fluorenylmethoxycarbonyl (Fmoc) group, and the hydrogen atoms on the alpha carbon are replaced with deuterium isotopes. This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS), where the Fmoc group serves as a protective group that can be easily removed under basic conditions. The incorporation of deuterium can be beneficial for various applications, including NMR spectroscopy and metabolic studies, as it provides a means to trace the compound in biological systems. The presence of the Fmoc group enhances the solubility and stability of the amino acid during synthesis. Overall, Fmoc-Gly-D2 is a valuable tool in the field of organic and medicinal chemistry, facilitating the development of peptides with specific isotopic labeling for research and therapeutic purposes.
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Found 4 products.
Glycine-2,2-d2-N-FMOC
CAS:Formula:HOOCCD2NHFMOCPurity:98 atom % DColor and Shape:White SolidMolecular weight:299.32N-Fmoc-glycine-d2
CAS:Controlled Product<p>Applications Isotope labelled N-Fmoc-glycine is an N-Fmoc-protected form of Glycine (G615990). Glycine is a nonessential amino acid that acts as an inhibitory neyrotransmitter in the vertebrate central nervous system. Glycine also posesses cytoprotective against oxidant damage in the kidney.<br>References Eulenberg, V., et al.: Trend. Biochem. Sci., 30, 325 (2005); Gundersen, R., et al.: Acta Anaesth. Scand., 49, 1108 (2005); Lockart, R. & Eagle, H.: Science, 129, 252 (1959); Sogabe, K., et al.: Kidn. Int., 50, 845 (1996)<br></p>Formula:C17H13D2NO4Color and Shape:NeatMolecular weight:299.32Fmoc-[D2]Gly-OH
CAS:Controlled Product<p>Fmoc-Gly is a synthetic amino acid that has been used in the synthesis of peptides and proteins. The Fmoc group is removed by an amidase to yield the desired peptide. Fmoc-gly can be quantified using matrix-assisted laser desorption/ionization mass spectrometry (MALDI-TOF). This technique is also used for the analysis of cellular uptake, intracellular localization, and metabolic stability. A laser is used to vaporize a sample and create ions. These ions are then analyzed with a mass spectrometer to generate a spectrum that can be matched with a database of known compounds. MALDI-TOF has been shown to be more efficient than other methods for peptide analysis such as electrospray ionization.</p>Formula:C17H13D2NO4Purity:Min. 95%Molecular weight:299.32 g/mol




