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Fmoc-L-Ala(2-Furyl)-OH
Nom chimique: N-alpha-(9-Fluorenylmethyloxycarbonyl)-3-(2-furyl)-L-alanine // Synonymes: Fmoc-2Fal-OH, (S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(furan-2-yl)propanoic acid, Fmoc-Ala(2-Furyl)-OH
- n° Art.:FAA4250
- n° CAS:159611-02-6
- Formule:C22H19NO5
- Storage temperature:2-8°C
- Masse moléculaire:377,39 g/mol
from 250,00 €
description
2-Furyl-alanine has a set of surprising properties, which make it a useful tool for site-specific chemical modification of proteins, furan-mediated nucleic acid crosslinking and solid phase-based peptide labeling. It also already has been used in construction of fluorescent probes via peptide labeling and in antibody drug conjugates for diagnostic and therapeutic purposes. As an electron rich diene it can be used in Diels-Alder reactions with an appropriate dienophile. Photoactivation leads to singlet oxygen (1O2) mediated furan-based labeling, which can be carried out in physiological aqueous solutions. Hence, it is a powerful ligation tool for fast and efficient peptide, protein and antibody modification.
references
Novel furan-oxidation based site-specific conjugation methodology for peptide labeling and antibody drug conjugates; presented at the 6th World ADC meeting October 19th-22nd 2015,San Diego, CA; An Van Den Bulcke, Eirini Antonatou, Willem Vannecke, Kurt Hoogewijs and Annemieke Madder;
M. Sletten, C. R. Bertozzi, Angew. Chem. Int. Ed. 2009; 48: 6974.
K. Stevens, A. Madder, Nucleic Acids Research 2009; 1555.
M. Op De Beeck, A. Madder, J. Am. Chem. Soc. 2011; 133: 796.
Op De Beeck, A. Madder, J. Am. Chem. Soc. 2012; 134: 10737.
A. Deceuninck, A. Madder, Chem. Commun. 2009; 340.
K. Hoogewijs, D. Buyst, J. M. Winne, J. C. Martins, A. Madder, Chem. Commun. 2013; 49: 2927.
M. J. Schmidt, A. Weber, M. Pott, W. Welteand, D. Summerer, ChemBioChem 2014; 15: 1755.
M. J. Schmidt, D. Summerer, Angew. Chem. Int. Ed. 2013; 52: 4690.
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