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Fmoc-3-amino-4,4,4-trifluoro-butyric acid (S)
Chemical name: (S)-3-(9-Fluorenylmethyloxycarbonyl)amino-4,4,4-trifluoro-butyric acid // Synonyms: (S)-Fmoc-3-amino-4,4,4-trifluoro-butyric acid
- Product code:FAA4270
- CAS No.:1310680-31-9
- Formula:C19H16F3NO4
- Storage temperature:2-8°C
- Molecular weight:379.33 g/mol
from $250.00
references
Fluorine teams up with water to restore inhibitor activity to mutant BPTI; S. Ye, B. Loll, A. A. Berger, U. Mulow, C. Alings, M. C. Wahl and B. Koksch; Chemical science (Royal Society of Chemistry : 2010) 2015; 6: 5246-5254. https://doi.org/10.1039/c4sc03227f
Fluorinated amino acids in amyloid formation: a symphony of size, hydrophobicity and á-helix propensity; U. I. M. Gerling, M. Salwiczek, C. D. Cadicamo, H. Erdbrink, C. Czekelius, S. L. Grage, P. Wadhwani, A. S. Ulrich, M. Behrends, G. Haufe and B. Koksch; Chem. Sci. 2014; 5: 819-830. https://doi.org/10.1039/c3sc52932k
Towards identifying preferred interaction partners of fluorinated amino acids within the hydrophobic environment of a dimeric coiled coil peptide; T. Vagt, E. Nyakatura, M. Salwiczek, C. Jackel and B. Koksch; Org Biomol Chem 2010; 8: 1382-6. https://doi.org/10.1039/b917205j
Position-dependent effects of fluorinated amino acids on the hydrophobic core formation of a heterodimeric coiled coil; M. Salwiczek, S. Samsonov, T. Vagt, E. Nyakatura, E. Fleige, J. Numata, H. Colfen, M. T. Pisabarro and B. Koksch; Chemistry 2009; 15: 7628-36. https://doi.org/10.1002/chem.200802136
Effects of fluorination on the folding kinetics of a heterodimeric coiled coil; M. Salwiczek and B. Koksch; Chembiochem : a European journal of chemical biology 2009; 10: 2867-70. https://doi.org/10.1002/cbic.200900518
Fluorine in a native protein environment--How the spatial demand and polarity of fluoroalkyl groups affect protein folding; C. Jackel, M. Salwiczek and B. Koksch; Angew Chem Int Ed Engl 2006; 45: 4198-203. https://doi.org/10.1002/anie.200504387
Evaluation of the molecular interactions of fluorinated amino acids with native polypeptides; C. Jackel, W. Seufert, S. Thust and B. Koksch; Chembiochem : a European journal of chemical biology 2004; 5: 717-20. https://doi.org/10.1002/cbic.200300840
The identification of á-ketoamides as potent inhibitors of hepatitis c virus nS3-4a proteinase; J. M. Bennett, A. D. Campbell, A. J. Campbell, M. G. Carr, R. M. Dunsdon, J. R. Greening, D. N. Hurst, N. S. Jennings, P. S. Jones, S. Jordan, P. B. Kay, M. A. O'Brien, J. King-Underwood, T. M. Raynham, C. S. Wilkinson, T. C. I. Wilkinson and F. X. Wilson; Bioorganic & Medicinal Chemistry Letters 2001; 11: 355-357. https://doi.org/10.1016/s0960-894x(00)00654-5
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