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Fmoc-L-Agb(Pbf)-OH
Chemischer Name: (S)-N-alpha-(9-Fluorenylmethyloxycarbonyl)-N'-2,2,4,6,7-pentamethyldihydrobenzofuran-5-sulfonyl-2-amino-4-guanidino-butyric acid // Synonyme: Fmoc-Agb(Pbf)-OH, Fmoc-Norarginine(Pbf)-OH, (S)-Fmoc-2-amino-5-(N'-Pbf-guanidino)-pentanoic acid,(S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-(3-((2,2,4,6,7-pentamethyl-2,3-dihydrobenzofuran- 5-yl)sulfonyl)guanidino)butanoic acid
- Art-Nr.:FAA8280
- CAS Nr.:1313054-32-8
- Formel:C33H38N4O7S
- Molare Masse:634,75 g/mol
Startet von 165,00 €
references
Design, Synthesis, Molecular Dynamics Simulation, and Functional Evaluation of a Novel Series of 26RFa Peptide Analogues Containing a Mono- or Polyalkyl Guanidino Arginine Derivative; K. Alim, B. Lefranc, J. Sopkova-de Oliveira Santos, C. Dubessy, M. Picot, J. A. Boutin, H. Vaudry, N. Chartrel, D. Vaudry, J. Chuquet and J. Leprince; Journal of medicinal chemistry 2018; 61: 10185-10197. doi: https://doi.org/10.1021/acs.jmedchem.8b01332
Structure-Activity Relationship Study of Cyclic Pentapeptide Ligands for Atypical Chemokine Receptor 3 (ACKR3); H. Sekiguchi, T. Kuroyanagi, D. Rhainds, K. Kobayashi, Y. Kobayashi, H. Ohno, N. Heveker, K. Akaji, N. Fujii and S. Oishi; Journal of medicinal chemistry 2018; 61: 3745-3751. doi: https://doi.org/10.1021/acs.jmedchem.8b00336
Peptide Macrocycle Inhibitor of Coagulation Factor XII with Subnanomolar Affinity and High Target Selectivity; S. J. Middendorp, J. Wilbs, C. Quarroz, S. Calzavarini, A. Angelillo-Scherrer and C. Heinis; Journal of medicinal chemistry 2017; 60: 1151-1158. doi: https://doi.org/10.1021/acs.jmedchem.6b01548
A parallel semisynthetic approach for structure-activity relationship studies of peptide YY; L. Albertsen, S. Ostergaard, J. F. Paulsson, J. C. Norrild and K. Stromgaard; ChemMedChem 2013; 8: 1505-13, 1422. doi: https://doi.org/10.1002/cmdc.201300290
Trypsin resistance of a decapeptide KISS1R agonist containing an Nomega-methylarginine substitution; T. Asami, N. Nishizawa, Y. Ishibashi, K. Nishibori, Y. Horikoshi, H. Matsumoto, T. Ohtaki and C. Kitada; Bioorg Med Chem Lett 2012; 22: 6328-32. doi: https://doi.org/10.1016/j.bmcl.2012.08.087
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