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Fmoc-N(oNv)-Gly-OH
Chemischer Name: N-alpha (9-Fluorenylmethyloxycarbonyl)-N-alpha-(o-nitroveratryl)-glycine // Synonyme: 2-((((9H-fluoren-9-yl)methoxy)carbonyl)(4,5-dimethoxy-2-nitrobenzyl)amino)acetic acid, N-alpha (9-Fluorenylmethyloxycarbonyl)-N-alpha-(4,5-dimethoxy-2-nitrobenzyl)-glycine
- Art-Nr.:FAA7350
- CAS Nr.:850859-64-2
- Formel:C26H24N2O8
- Molare Masse:492,48 g/mol
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description
Tag for internal solubilization, which can be cleaved by photolysis (350 nm) under ambient conditions. See also our product Fmoc-L-Cys(oNv)-OH (FAA3970), where o-nitroveratryl has been used for thiol protection.
This compound is a potential building block for the construction of (customized) peptide nucleic acids (PNAs) and for peptoid synthesis.
references
Synthesis, stability and optimized photolytic cleavage of 4-methoxy-2-nitrobenzyl backbone-protected peptides. Erik C. B. Johnson and Stephen B. H. Kent; Chem. Commun. 2006;
1557-1559. DOI: 10.1039/b600304d
Photomodulation of Protein Trans-Splicing Through Backbone Photocaging of the DnaE Split Intein; Luis Berrade, Youngeun Kwon, and Julio A. Camarero; ChemBioChem 2010; 11: 1368 -
1372. DOI: 10.1002/cbic.201000157
Karas J.A., Scanlon D.B., Forbes B.E., Vetter I., Lewis R.J., Gardiner J., Separovic F., Wade J.D., Hossain M.A.; 2-Nitroveratryl as a Photocleavable Thiol-Protecting Group for
Directed Disulfide Bond Formation in the Chemical Synthesis of Insulin; Chem. Eur. J. 2014; 20: 9549-9552. DOI: 10.1002/chem.201403574.
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