N2-[(1,1-Dimethylethoxy)carbonyl]-N6-[(2-propynyloxy)carbonyl]-L-lysine
![N2-[(1,1-Dimethylethoxy)carbonyl]-N6-[(2-propynyloxy)carbonyl]-L-lysine结构式](https://image.chemsrc.com/caspic/383/1202704-91-3.png)
N2-[(1,1-Dimethylethoxy)carbonyl]-N6-[(2-propynyloxy)carbonyl]-L-lysine结构式
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常用名 | N2-[(1,1-Dimethylethoxy)carbonyl]-N6-[(2-propynyloxy)carbonyl]-L-lysine | 英文名 | N2-[(1,1-Dimethylethoxy)carbonyl]-N6-[(2-propynyloxy)carbonyl]-L-lysine |
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| CAS号 | 1202704-91-3 | 分子量 | 328.36100 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C15H24N2O6 | 熔点 | N/A | |
| MSDS | 中文版 美版 | 闪点 | 73 °C | |
| 符号 |
GHS07 |
信号词 | Warning |
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Genetic encoding and labeling of aliphatic azides and alkynes in recombinant proteins via a pyrrolysyl-tRNA Synthetase/tRNA(CUA) pair and click chemistry.
J. Am. Chem. Soc. 131 , 8720-8721, (2009) We demonstrate that an orthogonal Methanosarcina barkeri MS pyrrolysyl-tRNA synthetase/tRNA(CUA) pair directs the efficient, site-specific incorporation of N6-[(2-propynyloxy)carbonyl]-L-lysine, containing a carbon-carbon triple bond, and N6-[(2-azidoethoxy)c... |
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Synthesis of threefold glycosylated proteins using click chemistry and genetically encoded unnatural amino acids.
ChemBioChem. 10 , 2858-2861, (2009)
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