Ne-Boc-L-lysine

Names

[ Name ]:
Ne-Boc-L-lysine

[Synonym ]:
Z-Lys(Boc)-OH
Ne-Boc-L-Lysine
NEPSILON-BOC-L-LYSINE
N-[(Benzyloxy)carbonyl]-N-{[(2-methyl-2-propanyl)oxy]carbonyl}lysine
N2-BENZYLOXYCARBONYL-N6-BOC-L-LYSINE
e-BOC-L-lysine.
MFCD00037221
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-lysine
H-L-LYS(BOC)-OH
L-Lysine, N-[(1,1-dimethylethoxy)carbonyl]-
L-LYSINE(BOC)
LYS(BOC)
Fmoc-Lys(Boc)-OH
Lysine derivative 1
N-(Tert-Butoxycarbonyl)-L-Lysine
Nε-Boc-L-lysine
N2-Benzyloxycarbonyl-N6-tert-butyloxycarbonyl-L-lysine
L-LYS(BOC)
Nε-Boc-Nα-Cbz-L-lysine
N6-Boc-L-lysine
Nepsilon-Boc-Nalpha-Cbz-L-Lysine
Nε-(tert-Butoxycarbonyl)-L-lysine
(S)-2-Amino-6-((tert-butoxycarbonyl)amino)hexanoic acid
LYSINE(BOC)-OH
(S)-2-(((Benzyloxy)carbonyl)amino)-6-((tert-butoxycarbonyl)amino)hexanoic acid
N2-benzyloxycarbonyl-N6-tert-butoxycarbonyl-L-lysine
H-Lys(Boc)-OH
L-Lysine, N6-((1,1-dimethylethoxy)carbonyl)-
AmbotzZAA1184
Lysine, N-[(1,1-dimethylethoxy)carbonyl]-N-[(phenylmethoxy)carbonyl]-
N-Cbz-N'-Boc-L-lysine
Nε-(tert-Butoxycarbonyl)-Nα-carbobenzoxy-L-lysine

Biological Activity

[Description]:

(S)-2-Amino-6-((tert-butoxycarbonyl)amino)hexanoic acid is a lysine derivative[1].

[Related Catalog]:

Research Areas >> Others

Signaling Pathways >> Others >> Others

[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]

[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144.

Chemical & Physical Properties

[ Density]:
1.1±0.1 g/cm3

[ Boiling Point ]:
412.9±40.0 °C at 760 mmHg

[ Melting Point ]:
250 °C (dec.)(lit.)

[ Molecular Formula ]:
C₁₁H₂₂N₂O₄

[ Molecular Weight ]:
246.303

[ Flash Point ]:
203.5±27.3 °C

[ Exact Mass ]:
246.157959

[ PSA ]:
101.65000

[ LogP ]:
0.74

[ Vapour Pressure ]:
0.0±2.1 mmHg at 25°C

[ Index of Refraction ]:
1.485

[ Storage condition ]:
2~8°C

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2924199090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2924199090

[ Summary ]:
2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Adding l-lysine derivatives to the genetic code of mammalian cells with engineered pyrrolysyl-tRNA synthetases.

Biochem. Biophys. Res. Commun. 371(4) , 818-22, (2008)

We report a method for site-specifically incorporating l-lysine derivatives into proteins in mammalian cells, based on the expression of the pyrrolysyl-tRNA synthetase (PylRS)-tRNA(Pyl) pair from Meth...

Evidence that malondialdehyde-derived aminoenimine is not a fluorescent age pigment.

Chem. Res. Toxicol. 14(5) , 473-5, (2001)

It has been suggested that protein modifications by malondialdehyde (MDA), a major product of lipid peroxidation, contribute to the fluorescence formation of lipofuscin. Although early studies propose...

Nanoassembly of surfactants with interfacial drug-interactive motifs as tailor-designed drug carriers.

Mol. Pharm. 10(1) , 187-98, (2013)

PEGylated lipopeptide surfactants carrying drug-interactive motifs specific for a peptide-nitroxide antioxidant, JP4-039, were designed and constructed to facilitate the solubilization of this drug ca...