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Fmoc-L-Tyr(Propargyl)-OH
Chemischer Name: N-alpha-(9-Fluorenylmethyloxycarbonyl)-O-propargyl-L-tyrosine // Synonyme: 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
- Art-Nr.:FAA3830
- CAS Nr.:1204595-05-0
- Formel:C27H23NO5
- Molare Masse:441,48 g/mol
Startet von 225,00 €
references
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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
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