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H-L-Lys(oNB)-OH*HCl
Nombre químico: N6-(((2-nitrobenzyl)oxy)carbonyl)-L-lysine // Sinónimos: H-L-Lys(2-NO2-Z), H-Lys(oNB)*HCl, ONBK, H-L-Lys(oNB)-OH*HCl, H-L-Lys(2-nitrobenzyloxycarbonyl) hydrochloride, o-nitrobenzyl-oxycarbonyl-N-epsilon-L-lysine hydrochloride,N-epsilon-(o-nitrobenzyloxyca rbonyl)-L-lysine, Net CAS: 750556-72-0
- Nº Artículo:FAA9345
- Nº CAS:228564-76-9
- Fórmula:C14H19N3O6*HCl
- Storage temperature:2-8°C
- Masa molecular:325,32*36,45 g/mol
- Pureza:min. 98.0%
from 96,00 €
description
Photocaged Lysine derivative that can be incorporated into proteins. The photolabile group of ONBK can be efficiently removed by 365 nm light to afford a free lysine residue.
references
A Facile System for Encoding Unnatural Amino Acids in Mammalian Cells; P. R. Chen, D. Groff, J. Guo, W. Ou, S. Cellitti, B. H. Geierstanger, P. G. Schultz; Angew. Chem. Int. Ed. 2009; 48(22): 4052-4055. https://doi.org/10.1002/anie.200900683
Site-Specific Engineering of Chemical Functionalities on the Surface of Live Hepatitis D Virus; S. Lin, H. Yan, L. Li, M. Yang, B. Peng, S. Chen, W. Li, P. R. Chen; Angew. Chem. Int. Ed. 2013; 52(52): 13970-13974. https://doi.org/10.1002/anie.201305787
Mechanism-Based Design of a Photoactivatable Firefly Luciferase; J. Zhao, S. Lin, Y. Huang, J. Zhao, P. R. Chen; J. Am. Chem. Soc. 2013; 135(20): 7410-7413. https://doi.org/10.1021/ja4013535
Spatiotemporal functional assembly of split protein pairs through a light-activated SpyLigation; E. R: Ruskowitz, B. G. Munoz-Robles, A. C. Strange, C. H. Butcher, S. Kurniawan, J. R. Filteau, C. A. DeForest; Nature Chem. 2023; 15: 694-704. https://doi.org/10.1038/s41557-023-01152-x
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All information contained in our webshop is compiled to the best of our knowledge.
Prices and product availability are subject to change and require reconfirmation. Please contact us for further information.
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