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Fmoc-L-Tyr(Propargyl)-OH
Nombre químico: N-alpha-(9-Fluorenylmethyloxycarbonyl)-O-propargyl-L-tyrosine // Sinónimos: Fmoc-Tyr(Propargyl)-OH, Fmoc-Tyr(Propargyl), N-Fmoc-O-2-propyn-1-yl-L-tyrosine, (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(prop-2-yn-1-yloxy)phenyl)propanoic acid
- Nº Artículo:FAA3830
- Nº CAS:1204595-05-0
- Fórmula:C27H23NO5
- Storage temperature:2-8°C
- Masa molecular:441,48 g/mol
from 225,00 €
references
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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
The Discovery of Macrocyclic XIAP Antagonists from a DNA-Programmed Chemistry Library, and Their Optimization To Give Lead Compounds with in Vivo Antitumor Activity; B. A. Seigal, W. H. Connors, A. Fraley, R. M. Borzilleri, P. H. Carter, S. L. Emanuel, J. Fragnoli, K. Kim, M. Lei, J. G. Naglich, M. E. Pokross, S. L. Posy, H. Shen, N. Surti, R. Talbott, Y. Zhang, N. K. Terrett; J. Med. Chem. 2015; 58(6): 2855–2861. https://doi.org/10.1021/jm501892g
Effective PHIP Labeling of Bioactive Peptides Boosts the Intensity of the NMR Signal; G. Sauer, D. Nasu, D. Tietze, T. Gutmann, S. Englert, O. Avrutina, H. Kolmar, G. Buntkowsky; Angew. Chem. Int. Ed. 2014, 53(47): 12941-12945. https://doi.org/10.1002/anie.201404668
Ultrafast Single-Scan 2D NMR Spectroscopic Detection of a PHIP-Hyperpolarized Protease Inhibitor; A. S. Kiryutin; G. Sauer, D. Tietze, M. Brodrecht, S. Knecht, A. V. Yurkovskaya, K. L. Ivanov, O. Avrutina, H. Kolmar, G. Buntkowsky; Chem.-Eur. J. 2019; 25(16): 4025-4030. https://doi.org/10.1002/chem.201900079
Conjugation Strategy Strongly Impacts the Conformational Stability of a PEG-Protein Conjugate; P. B. Lawrence, W. M. Billings, M. B. Miller, B. K. Pandey, A. R. Stephens, M. I. Langlois, J. L. Price; ACS Chem. Biol. 2016; 11(7): 1805–1809. https://doi.org/10.1021/acschembio.6b00349
In Vitro Membrane Permeation Studies and in Vivo Antinociception of Glycosylated Dmt1-DALDA Analogues; S. Ballet, C. Betti, A. Novoa, C. Tömböly, C. U. Nielsen, H. C. Helms, A. Lesniak, P. Kleczkowska, N. N. Chung, A. W. Lipkowski, B. Brodin, D. Tourwe, P. W. Schiller; ACS Med. Chem. Lett. 2014, 5(4): 352–357. https://doi.org/10.1021/ml4004765
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All information contained in our webshop is compiled to the best of our knowledge.
Prices and product availability are subject to change and require reconfirmation. Please contact us for further information.
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