Fmoc-Lys(Biotin)-OH

Names

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

[Synonym ]:
MFCD00270741
(2S)-6-[5-[(3aS,4S,6aR)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]pentanoylamino]-2-(9H-fluoren-9-ylmethoxycarbonylamino)hexanoic acid
L-Lysine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-[5-[(3aS,4S,6aR)-hexahydro-2-oxo-1H-thieno[3,4-d]imidazol-4-yl]-1-oxopentyl]-
Fmoc-N-epsilon-biotinyl-L-lysine
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-{5-[(3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl]pentanoyl}-L-lysine
Fmoc-Lys(Biotin)-OH

Biological Activity

[Description]:

Fmoc-Lys(Biotin)-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]:
1.3±0.1 g/cm3

[ Boiling Point ]:
936.2±65.0 °C at 760 mmHg

[ Melting Point ]:
183 °C

[ Molecular Formula ]:
C₃₁H₃₈N₄O₆S

[ Molecular Weight ]:
594.722

[ Flash Point ]:
520.0±34.3 °C

[ Exact Mass ]:
594.251221

[ PSA ]:
171.16000

[ LogP ]:
3.20

[ Vapour Pressure ]:
0.0±0.3 mmHg at 25°C

[ Index of Refraction ]:
1.594

[ Storage condition ]:
-15°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

[ Safety Phrases ]:
S22-S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Articles

Synthesis and characterization of site-specific biotinylated probes for the motilin receptor.

Int. J. Pept. Protein Res. 44 , 582, (1994)

The solid-phase synthesis of two porcine motilin derivatives, specifically biotinylated on the side chain of Lys20, was accomplished by preactivation of the protected amino acids N alpha-(9-fluorenylm...