Fmoc-L-Cys(Propargyl)-OH

Nombre químico: N-alpha-(9-Fluorenylmethyloxycarbonyl)-S-propargyl-L-cysteine // Sinónimos: Fmoc-Cys(Propargyl)-OH

  • Nº Artículo:FAA3810
  • Nº CAS:1354752-76-3
  • Fórmula:C21H19NO4S
  • Storage temperature:-20°C
  • Masa molecular:381,44 g/mol

from 250,00 €

Grouped product items
Cantidad Unidad de venta Precio Unidad de almacenamiento de stock (SKU) Disponibilidad
1 g
250,00 €
FAA3810.0001
<10 días laborables
5 g
1.000,00 €
FAA3810.0005
<10 días laborables
Hoja de seguridad
references

Development of 6-[(18) F]fluoro-carbohydrate-based prosthetic groups and their conjugation to peptides via click chemistry; C. Collet, F. Maskali, A. Clement, F. Chretien, S. Poussier, G. Karcher, P. Y. Marie, Y. Chapleur and S. Lamande-Langle; J Labelled Comp Radiopharm 2016; 59: 54-62. https://doi.org/10.1002/jlcr.3362

'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

Toward Imaging Glycotools by Click Coupling; Y. Chapleur, C. Vala, F. Chrétien and S. Lamandé-Langle; Click Chemistry in Glycoscience 2013: 183-210. https://doi.org/10.1002/9781118526996.ch7

Neoglycopeptides through direct functionalization of cysteine; C. Vala, F. Chrétien, E. Balentova, S. Lamandé-Langle and Y. Chapleur; Tetrahedron Letters 2011; 52: 17-20. https://doi.org/10.1016/j.tetlet.2010.10.021

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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