Top Suppliers:I want be here

146987-10-2

146987-10-2 structure
146987-10-2 structure

Name Nα-Fmoc-Nε-biotinyl-L-lysine
Synonyms Fmoc-L-Lys(biotinyl)-OH
FMOC-L-LYS(BIOTIN)-OH
N-(9-Fluorenylmethyloxycbonyl)-N'-biotinyl-L-lysine
Nα-FMoc-Nε-biotinyl- L -lysine
FMOC-LYS(BIOTIN)-OH
Nα-FMoc-Nε-biotinyl-L-lysine
(S)-2-(Fmoc-amino)-6-[5-[(3aS,4S,6-2-oxohexahydro-4-thieno[3,4-d]imidazolyl]pentanamido]hexanoic Acid
N^a-Biotinyl-N^e-FMoc-L-lysine
NALPHA-BIOTINYL-NSILON-FMOC-L-LYSINE
N-ALPHA-FMOC-N-SILON-D-BIOTINYL-L-LYSINE
(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
Fmoc-Lys(biotinyl)-OH, Nα-Biotinyl-Nε-Fmoc-L-lysine
N-ALPHA-FMOC-N-SILON-BIOTINYL-L-LYSINE
Fmoc-Lys(Biotin)-OH(N-a-Fmoc-N-e-(d-Biotin)-L-lysine
(9H-Fluoren-9-yl)MethOxy]carbonyl Lys(Biotin)-OH
N-ALPHA-(9-FLUORENYLMETHYLOXYCBONYL)-N-SILON-BIOTINYL-L-LYSINE
Nα-[(9H-Fluoren-9-ylmethoxy)carbonyl]-Nε-biotinyl-L-lysine>
FMOC-LYS(BIOT)-OH
FMOC-N-SILON-BIOTINYL-L-LYSINE
FMOC-LYS(BIOTIN)
L-Lysine, N2-[(9H-fluoren-9-ylmethoxy)carbonyl]-N6-[5-[(3aS,4S,6-hexahydro-2-oxo-1H-thieno[3,4-d]imidazol-4-yl]-1-oxopentyl]
N-ALPHA-(9-FLUORENYLMETHOXYCBONYL)-N-SILON-BIOTINYL-L-LYSINE
Nα-[(9H-Fluoren-9-ylmethoxy)carbonyl]-Nε-biotinyl-L-lysine
ε-Biotinoyl-α-(9-fluorenylmethoxycbonyl)-L-lysine
FMOC-LYS(EXTENDED*-BIOTIN)
Fmoc-N-epsilon-biotinyl-L-lysine
N-ALPHA-FMOC-N-SILON-(D-BIOTIN)-L-LYSINE
FMOC-LYS(BIOTINYL)-OH
(2S)-6-[5-[(3aS,4S,6-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]pentanoylamino]-2-(9H-fluoren-9-ylmethoxycbonylamino)hexanoic acid
FMOC-LYS(BIOTIN)-OH //BP
SILON-BIOTINOYL-ALPHA-(9-FLUORENYLMETHOXYCBONYL)-L-LYSINE
2-[[9H-fluoren-9-ylmethoxy(oxo)methyl]amino]-6-[[1-oxo-5-(2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl)pentyl]amino]hexanoic acid
biotinyl- L -lysine
(S)-2-(((9H-FLUOREN-9-YL)METHOXY)CBONYLAMINO)-6-(5-((3AS,4S,6-2-OXO-HEXAHYDRO-1H-THIENO[3,4-D]IMIDAZOL-4-YL)PENTANAMIDO)HEXANOIC ACID
Nalpha-[(9H-Fluoren-9-ylmethoxy)carbonyl]-Nsilon-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
Nα-Fmoc-Nε-biotinyl-L-lysine (HPLC)
(S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-6-(5-((3aS,4S,6-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamido)hexanoic acid
(2S)-6-{5-[(3aS,4S,6-2-oxo-hexahydro-1H-thieno[3,4-d]imidazol-4-yl]pentanamido}-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)hexanoic acid
MFCD00270741
FMOC-K(BIOTIN)-OH
Nalpha-[(9H-Fluoren-9-ylmethoxy)carbonyl]-Nsilon-biotinyl-L-lysine, (HPLC)
Fmoc-Lys(biotin)-OH Novabiochem
FMOC-LYSINE(BIOTINYL)-OH
N-ALPHA-(9-FLUORENYLMETHOXYCBONYL)-L-BIOCYTIN
FMOC-BCT-OH
FMOC BIOCYTIN
Description Fmoc-Lys(Biotin)-OH is a lysine derivative[1].
Related Catalog
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.

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
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

~82%

146987-10-2 structure

146987-10-2

Literature: Feng, Siliang; Li, Senhao; Kang, Xiaoyu; Liu, Keliang Journal of Chemical Research, 2010 , # 6 p. 348 - 350

~%

146987-10-2 structure

146987-10-2

Literature: Wang, Jun; Uttamchandani, Mahesh; Li, Ping Sun; Yao, Shao Q. Chemical Communications, 2006 , # 7 p. 717 - 719

~%

146987-10-2 structure

146987-10-2

Literature: Chemical Communications, , # 7 p. 717 - 719

~%

146987-10-2 structure

146987-10-2

Literature: Chemical Communications, , # 7 p. 717 - 719
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.