Fmoc-D-Agb-OH*HCl

Chemical name: (R)-N-alpha-(9-Fluorenylmethyloxycarbonyl)-2-amino-4-guanidino-butyric acid hydrochloride // Synonyms: (R)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-4-(diaminomethyleneamino)butanoic acid, 2-(Fmoc-amino)-4-guanidino-D-butyric acid, Fmoc-D-Agb*HCl, Fmoc-D-Nar*HCl,Fmoc-D-norArg*HCl, Fmoc-D-Norarginin e hydrochloride

  • Product code:FAA7680
  • CAS No.:2741370-51-2 net
  • Formula:C20H22N4O4*HCl
  • Storage temperature:2-8°C
  • Molecular weight:382.41*36.45 g/mol
  • Purity :min. 98%
  • Enantiomeric Purity:min. 99,7%

from €100.00

Grouped product items
Qty Packing unit Price SKU Availability
250 mg
€100.00
FAA7680.0250
<10 business days
500 mg
€180.00
FAA7680.0500
<10 business days
1 g
€280.00
FAA7680.1000
<10 business days
5 g
€1,000.00
FAA7680.5000
Please inquire
description

Used as a protected Arginine homologue in peptide synthesis. The guanidino-group is protected by protonation, which can be restored after Fmoc-cleavage by pre-washing of the peptide with pyridine hydrobromide (0.08M in DMF) for 10min. prior to the next coupling.

references

Trypsin resistance of a decapeptide KISS1R agonist containing an Nù-methylarginine substitution.

Asami T., Nishizawa N., Ishibashi Y., Nishibori K., Horikoshi Y., Matsumoto H., Ohtaki T., Kitada C.; Bioorg Med Chem Lett. 2012; 22(20): 6328-6332. DOI: 10.1016/j.bmcl.2012.08.087.

Peptide Macrocycle Inhibitor of Coagulation Factor XII with Subnanomolar Affinity and High Target Selectivity; Simon J. Middendorp, Jonas Wilbs, Claudia Quarroz, Sara Calzavarini, Anne Angelillo-Scherrer, Christian Heinis; J. Med. Chem. 2017; 60(3): 1151-1158. DOI: 10.1021/acs.jmedchem.6b01548;

Design, Synthesis, Molecular Dynamics Simulation, and Functional Evaluation of a Novel Series of 26RFa Peptide Analogues Containing a Mono- or Polyalkyl Guanidino Arginine Derivative; Karima Alim, Benjamin Lefranc, Jana Sopkova-de Oliveira Santos, Christophe Dubessy, Marie Picot, Jean A. Boutin, Hubert Vaudry, Nicolas Chartrel, David Vaudry, Julien Chuquet, Jérôme Leprince; J. Med. Chem. 2018; 61(22): 10185-10197. DOI: 10.1021/acs.jmedchem.8b01332.


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