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Fmoc-L-DfAbu-OH
Chemical name: S)-2-(9-Fluorenylmethyloxycarbonyl)amino-4,4-difluorobutyric acid // Synonyms: Fmoc-L-DfeGly-OH, Fmoc-(2,2-difluoroeth-1-yl)-L-glycine, Fmoc-L-4,4-F2Abu-OH, (S)-Fmoc-2-amino-4,4-difluorobutyric acid, (S)-Fmoc-2-amino-4,4-difluorobutanoic acid,(S)-2-((((9H-fluoren-9-yl)methoxy) carbonyl)amino)-4,4-difluorobutanoic acid, Fmoc-Df
- Product code:FAA8365
- CAS No.:467442-21-3
- Formula:C19H17F2NO4
- Storage temperature:2-8°C
- Molecular weight:361.34 g/mol
from $281.25
references
Phe*-Ala-based pentapeptide mimetics are BACE inhibitors: P2 and P3 SAR; J. Lamar, J. Hu, A. B. Bueno, H. C. Yang, D. Guo, J. D. Copp, J. McGee, B. Gitter, D. Timm, P. May, J. McCarthy and S. H. Chen; Bioorg Med Chem Lett 2004; 14: 239-43. https://doi.org/10.1016/j.bmcl.2003.09.084
SAR and pharmacokinetic studies on phenethylamide inhibitors of the hepatitis C virus NS3/NS4A serine protease; S. Malancona, S. Colarusso, J. M. Ontoria, A. Marchetti, M. Poma, I. Stansfield, R. Laufer, A. Di Marco, M. Taliani, M. Verdirame, O. Gonzalez-Paz, V. G. Matassa and F. Narjes; Bioorg Med Chem Lett 2004; 14: 4575-9. https://doi.org/10.1016/j.bmcl.2004.05.093
Novel, potent phenethylamide inhibitors of the hepatitis C virus (HCV) NS3 protease: probing the role of P2 aryloxyprolines with hybrid structures; F. Orvieto, U. Koch, V. G. Matassa and E. Muraglia; Bioorg Med Chem Lett 2003; 13: 2745-8. https://doi.org/10.1016/s0960-894x(03)00536-5
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