Z-Lys-OH

Names

[ Name ]:
Z-Lys-OH

[Synonym ]:
α-Carbobenzoxy-L-lysine
Z-Lys-OH
N-α-Benzyloxycarbonyl-L-lysine
cbz-l-lysine
N-[(Benzyloxy)carbonyl]-L-lysine
Nα-Z-L-Lysine
N-α-Carbobenzoxy-L-lysine
Cbz-Lys-OH
e-carbobenzyloxy-L-lysine
carbobenzoxy-L-lysine
EINECS 218-662-6
Nalpha-Z-L-Lysine
CBZ-L-Lys-OH
Z-lysine
Nalpha-(Carbobenzyloxy)-L-lysine
Nalpha-Cbz-L-lysine
L-Lysine, N-[(phenylmethoxy)carbonyl]-
Nα-(Carbobenzyloxy)-L-lysine
N-α-Cbz-L-lysine
MFCD00038204
(S)-6-Amino-2-(((benzyloxy)carbonyl)amino)hexanoic acid
n-|A-carbobenzoxy-l-lysine
Nα-Cbz-L-lysine
N(α)-Cbz-L-lysine
N2-Cbz-L-lysine
Nα-Carbobenzoxy-L-lysine
N-Carbobenzoxy-L-lysine
N-alpha-Cbz-L-lysine

Biological Activity

[Description]:

Z-Lys-OH 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]:
1.2±0.1 g/cm3

[ Boiling Point ]:
497.0±45.0 °C at 760 mmHg

[ Melting Point ]:
226-231 °C (dec.)(lit.)

[ Molecular Formula ]:
C₁₄H₂₀N₂O₄

[ Molecular Weight ]:
280.320

[ Flash Point ]:
254.4±28.7 °C

[ Exact Mass ]:
280.142303

[ PSA ]:
101.65000

[ LogP ]:
1.36

[ Vapour Pressure ]:
0.0±1.3 mmHg at 25°C

[ Index of Refraction ]:
1.550

MSDS

Click to get detail MSDS

Safety Information

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

[ Hazard Codes ]:
Xn

[ Risk Phrases ]:
R20/21/22

[ Safety Phrases ]:
S22-S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2924299090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2924299090

[ Summary ]:
2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Nanofibrous spongy microspheres enhance odontogenic differentiation of human dental pulp stem cells.

Adv. Healthc. Mater. 4 , 1993-2000, (2015)

Dentin regeneration is challenging due to its complicated anatomical structure and the shortage of odontoblasts. In this study, a novel injectable cell carrier, nanofibrous spongy microspheres (NF-SMS...

Characterization of Nalpha-benzyloxycarbonyl-L-lysine oxidizing enzyme from Rhodococcus sp. AIU Z-35-1.

J. Biosci. Bioeng. 104(3) , 218-23, (2007)

An oxidase catalyzing conversion of N(alpha)-benzyloxycarbonyl-L-lysine (N(alpha)-Z-L-lysine) to N(alpha)-benzyloxycarbonyl-L-aminoadipate-delta-semialdehyde (N(alpha)-Z-L-AASA) was purified from Rhod...

The pH dependency of bovine spleen cathepsin B-catalyzed transfer of N alpha-benzyloxycarbonyl-L-lysine from p-nitrophenol to water and dipeptide nucleophiles. Comparisons with papain.

J. Biol. Chem. 258(3) , 1650-5, (1983)

Cathepsin B has been shown to catalyze the transfer of the N alpha-benzyloxycarbonyl-L-lysyl residue from the corresponding p-nitrophenyl ester substrate to water and dipeptide nucleophiles. These rea...