N2-[(1,1-Dimethylethoxy)carbonyl]-N6-[(2-propynyloxy)carbonyl]-L-lysine structure
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Common Name | N2-[(1,1-Dimethylethoxy)carbonyl]-N6-[(2-propynyloxy)carbonyl]-L-lysine | ||
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CAS Number | 1202704-91-3 | Molecular Weight | 328.36100 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C15H24N2O6 | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | 163.4 °F | |
Symbol |
GHS07 |
Signal Word | Warning |
Use of N2-[(1,1-Dimethylethoxy)carbonyl]-N6-[(2-propynyloxy)carbonyl]-L-lysineN2-[(1,1-Dimethylethoxy)carbonyl]-N6-[(2-propynyloxy)carbonyl]-L-lysine is a lysine derivative[1]. |
Name | Boc-Lys(Poc)-OH |
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Synonym | More Synonyms |
Description | N2-[(1,1-Dimethylethoxy)carbonyl]-N6-[(2-propynyloxy)carbonyl]-L-lysine is a lysine derivative[1]. |
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Related Catalog | |
In Vitro | Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1]. |
References |
Molecular Formula | C15H24N2O6 |
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Molecular Weight | 328.36100 |
Exact Mass | 328.16300 |
PSA | 113.96000 |
LogP | 2.27580 |
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, conta... |
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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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(S)-2-(tert-butoxycarbonylamino)-6-((prop-2-ynyloxy)carbonylamino)hexanoic acid |