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Fmoc-L-TFM-OH
Nom chimique: N-alpha-(9-Fluorenylmethyloxycarbonyl)-S-trifluoromethyl-L-methionine // Synonymes: Fmoc-TFM-OH, (S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-4-(trifluoromethylthio)butanoic acid
- n° Art.:FAA4570
- n° CAS:928654-78-8
- Formule:C20H18F3NO4S
- Masse moléculaire:425,42 g/mol
Starting at 275,00 €
references
Strategy for "detoxification" of a cancer-derived histone mutant based on mapping its interaction with the methyltransferase PRC2; Z. Z. Brown, M. M. Muller, S. U. Jain, C. D. Allis, P. W. Lewis and T. W. Muir; J Am Chem Soc 2014; 136: 13498-501. DOI: https://doi.org/10.1021/ja5060934.
Resolution of oligomeric species during the aggregation of Abeta1-40 using (19)F NMR; Y. Suzuki, J. R. Brender, M. T. Soper, J. Krishnamoorthy, Y. Zhou, B. T. Ruotolo, N. A. Kotov, A. Ramamoorthy and E. N. Marsh; Biochemistry 2013; 52: 1903-12. DOI: https://doi.org/10.1021/bi400027y.
Reduction potential tuning of the blue copper center in Pseudomonas aeruginosa azurin by the axial methionine as probed by unnatural amino acids; D. K. Garner, M. D. Vaughan, H. J. Hwang, M. G. Savelieff, S. M. Berry, J. F. Honek and Y. Lu; J Am Chem Soc 2006; 128: 15608-17. DOI: https://doi.org/10.1021/ja062732i.
Syntheses of and chemotactic responses elicited by fMet-Leu-Phe analogs containing difluoro- and trifluoromethionine; M. E. Houston, L. Harvath and J. F. Honek; Bioorganic & Medicinal Chemistry Letters 1997; 7: 3007-3012. DOI: https://doi.org/10.1016/s0960-894x(97)10134-2.
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