Fmoc-Lys(Dabcyl)-OH

Names

[ Name ]:
Fmoc-Lys(Dabcyl)-OH

[Synonym ]:
Fmoc-Lys(Dabcyl)-OH
N|A-4-[4-(Dimethylamino)phenylazo)benzoyl]-N|A-Fmoc-L-lysine
AmbotzFAA1498
N|A-Fmoc-N|A-Dabcyl-L-lysine
Fmoc-Lys(Dadcyl)-OH
Nepsilon-4-[4-(Dimethylamino)phenylazo)benzoyl]-Nalpha-Fmoc-L-lysine
Nalpha-Fmoc-Nepsilon-Dabcyl-L-lysine
N6-[4-[[4-(Dimethylamino)phenyl]azo]benzoyl]-N2-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-lysine

Biological Activity

[Description]:

Fmoc-Lys(Dabcyl)-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]:
1.26

[ Molecular Formula ]:
C₃₆H₃₇N₅O₅

[ Molecular Weight ]:
619.70900

[ Exact Mass ]:
619.27900

[ PSA ]:
136.18000

[ LogP ]:
7.65530

[ Appearance of Characters ]:
Crystalline Powder | Red

[ 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

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Articles

Automated Synthesis of Fluorogenic Protease Substrates: Design of Probes for Alzheimers Disease-Associated Proteases. Wang, G.T., et al.

Bioorg. Med. Chem. Lett. 2 , 1665, (1992)

Q.M. Wang et al.

Antiviral Chem. Chemother. 8 , 303, (1997)