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Fmoc-L-Ser(Propargyl)-OH
Nom chimique: N-alpha-(9-Fluorenylmethyloxycarbonyl)-O-propargyl-L-serine // Synonymes: Fmoc-Ser(Propargyl)-OH
- n° Art.:FAA3820
- n° CAS:1354752-75-2
- Formule:C21H19NO5
- Storage temperature:2-8°C
- Masse moléculaire:365,38 g/mol
from 150,00 €
references
'Click' glycosylation of peptides through cysteine propargylation and CuAAC; S. Lamande-Langle, C. Collet, R. Hensienne, C. Vala, F. Chretien, Y. Chapleur, A. Mohamadi, P. Lacolley and V. Regnault; Bioorg Med Chem 2014; 22: 6672-6683. https://doi.org/10.1016/j.bmc.2014.09.056
Photoinduced addition of glycosyl thiols to alkynyl peptides: use of free-radical thiol-yne coupling for post-translational double-glycosylation of peptides; M. Lo Conte, S. Pacifico, A. Chambery, A. Marra and A. Dondoni; J Org Chem 2010; 75: 4644-7. https://doi.org/10.1021/jo1008178
Lacosamide isothiocyanate-based agents: novel agents to target and identify lacosamide receptors; K. D. Park, P. Morieux, C. Salome, S. W. Cotten, O. Reamtong, C. Eyers, S. J. Gaskell, J. P. Stables, R. Liu and H. Kohn; Journal of medicinal chemistry 2009; 52: 6897-911. https://doi.org/10.1021/jm9012054
On the function and structure of synthetically modified porins; S. Reitz, M. Cebi, P. Reiss, G. Studnik, U. Linne, U. Koert and L. O. Essen; Angew Chem Int Ed Engl 2009; 48: 4853-7. https://doi.org/10.1002/anie.200900457
Non-enzymatic covalent protein labeling using a reactive tag; H. Nonaka, S. Tsukiji, A. Ojida and I. Hamachi; J Am Chem Soc 2007; 129: 15777-9. https://doi.org/10.1021/ja074176d
Isoxazolyl-serine-based agonists of peroxisome proliferator-activated receptor: design, synthesis, and effects on cardiomyocyte differentiation; Z. L. Wei, P. A. Petukhov, F. Bizik, J. C. Teixeira, M. Mercola, E. A. Volpe, R. I. Glazer, T. M. Willson and A. P. Kozikowski; J Am Chem Soc 2004; 126: 16714-5. https://doi.org/10.1021/ja046386l
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