Fmoc-L-DFM-OH

Nom chimique: N-alpha-(9-Fluorenylmethyloxycarbonyl)-S-difluoromethyl-L-methionine // Synonymes: Fmoc-DFM-OH, (S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-4-(difluoromethylthio)butanoic acid, N-(((9H-fluoren-9-yl)methoxy)carbonyl)-S-(difluoromethyl)-L-homocysteine

  • n° Art.:FAA8380
  • n° CAS:928654-74-4
  • Formule:C20H19F2NO4S
  • Storage temperature:2-8°C
  • Masse moléculaire:407,43 g/mol

from 2 500,00 €

Grouped product items
Nombre Unité de vente Prix SKU Disponibilité
1 g
2 500,00 €
FAA8380.0001
sur demande
references

Intriguing cellular processing of a fluorinated amino acid during protein biosynthesis in Escherichia coli; M. D. Vaughan, Z. Su, E. Daub and J. F. Honek; Org Biomol Chem 2016; 14: 8942-8946. https://doi.org/10.1039/c6ob01690a

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. https://doi.org/10.1021/ja062732i

Difluoromethionine as a Novel19F NMR Structural Probe for Internal Amino Acid Packing in Proteins; P. Cleve, V. Robinson, H. S. Duewel and J. F. Honek; Journal of the American Chemical Society 1999; 121: 8475-8478. https://doi.org/10.1021/ja9911418

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. https://doi.org/10.1016/s0960-894x(97)10134-2


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