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Boc-3-amino-4,4,4-trifluoro-butyric acid (R)
Nom chimique: (R)-3-t-Butyloxycarbonylamino-4,4,4-trifluoro-butyric acid // Synonymes: (R)-Boc-3-amino-4,4,4-trifluoro-butyric acid
- n° Art.:BAA2890
- n° CAS:1310680-29-5
- Formule:C9H14F3NO4
- Storage temperature:2-8°C
- Masse moléculaire:257,21 g/mol
from 600,00 €
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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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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