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Merck

774995

Sigma-Aldrich

N2-[(1,1-Dimethylethoxy)carbonyl]-N6-[(2-propynyloxy)carbonyl]-L-lysine

90%

别名:

N-α-Boc-propargyl-lysine-OH

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About This Item

经验公式(希尔记法):
C15H24N2O6
分子量:
328.36
MDL號碼:
分類程式碼代碼:
12352200
PubChem物質ID:
NACRES:
NA.22

化驗

90%

形狀

liquid

反應適用性

reaction type: click chemistry

折射率

n20/D 1.475

密度

1.167 g/mL at 25 °C

SMILES 字串

CC(C)(C)OC(=O)N[C@@H](CCCCNC(=O)OCC#C)C(O)=O

InChI

1S/C15H24N2O6/c1-5-10-22-13(20)16-9-7-6-8-11(12(18)19)17-14(21)23-15(2,3)4/h1,11H,6-10H2,2-4H3,(H,16,20)(H,17,21)(H,18,19)/t11-/m0/s1

InChI 密鑰

VHCJWKDEXGPNCX-NSHDSACASA-N

應用

Alkyne modified lysine that has been shown to be incorporated site-specifically into recombinant proteins.

相關產品

象形圖

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訊號詞

Warning

危險聲明

防範說明

危險分類

Skin Sens. 1

儲存類別代碼

10 - Combustible liquids not in Storage Class 3

水污染物質分類(WGK)

WGK 3

閃點(°F)

164.0 °F

閃點(°C)

73.33 °C


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分析证书(COA)

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Slide 1 of 1

1 of 1

Duy P Nguyen et al.
Journal of the American Chemical Society, 131(25), 8720-8721 (2009-06-12)
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)carbonyl]-L-lysine, containing an azido group, into recombinant proteins in Escherichia coli. Proteins containing the alkyne functional
Synthesis of threefold glycosylated proteins using click chemistry and genetically encoded unnatural amino acids.
Emine Kaya et al.
Chembiochem : a European journal of chemical biology, 10(18), 2858-2861 (2009-11-10)

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