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Fmoc-L-Lys(Boc,Fructose)-OH
Chemischer Name: N-alpha-(9-Fluorenylmethyloxycarbonyl)-N-epsilon-[6-(t-butyloxycarbonyl)aminohexanoyl]-N-epsilon-(2,3:4,5-di-O-isopropylidene-1-deoxyfructopyranosyl)-L-lysine // Synonyme: Fmoc-L-Lys(Boc)(2,3:4,5-di-O-isopropylidene-1-deoxyfructopyranosyl)-OH,(S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-6-(tert-butoxycarbonyl(((3aS,5aR,8aS,8bR)-2,2,7,7-tetramethyltetrahydro-3aH-bis [1,3]dioxolo[4,5-b:4',5'-d]pyran-3a-yl)methyl)amin
- Art-Nr.:FAA5540
- CAS Nr.:1133875-59-8
- Formel:C38H50N2O11
- Molare Masse:710,82 g/mol
Startet von 250,00 €
description
Fructose conjugated lysine building block for solid phase peptide synthesis of Amadori-modified peptides.
references
Building blocks for the synthesis of post-translationally modified glycated peptides and proteins; S. Carganico, P. Rovero, J. A. Halperin, A. M. Papini and M. Chorev; J Pept Sci 2009; 15: 67-71. https://doi.org/10.1002/psc.1105
A new procedure for the synthesis of peptide-derived Amadori products on a solid support; P. Stefanowicz, K. Kapczyńska, A. Kluczyk and Z. Szewczuk; Tetrahedron Letters 2007; 48: 967-969. https://doi.org/10.1016/j.tetlet.2006.12.022
Site-specific synthesis of Amadori-modified peptides on solid phase; A. Frolov, D. Singer and R. Hoffmann; J Pept Sci 2006; 12: 389-95. https://doi.org/10.1002/psc.739
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