T1660
Nε,Nε,Nε-三甲基赖氨酸 盐酸盐
≥97% (TLC)
别名:
1-Pentanaminium, 5-amino-5-carboxy-N,N,N-trimethyl-, chloride (1:1), (5S)-
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关于此项目
经验公式（希尔记法）:
C9H20N2O2 · HCl
化学文摘社编号:
分子量:
224.73
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352202
MDL number:
InChI
1S/C9H20N2O2.ClH/c1-11(2,3)7-5-4-6-8(10)9(12)13;/h8H,4-7,10H2,1-3H3;1H/t8-;/m0./s1
SMILES string
[Cl-].C[N+](C)(C)CCCC[C@H](N)C(O)=O
InChI key
ZKIJKCHCMFGMCM-QRPNPIFTSA-N
assay
≥97% (TLC)
form
powder
contains
salts and water as balance
composition
Amino acid content, ~75%
technique(s)
LC/MS: suitable
color
white
storage temp.
−20°C
Quality Level
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Sara P Gaucher et al.
Journal of proteome research, 7(6), 2320-2331 (2008-04-18)
Recent developments in shotgun proteomics have enabled high-throughput studies of a variety of microorganisms at a proteome level and provide experimental validation for predicted open reading frames in the corresponding genome. More importantly, advances in mass spectrometric data analysis now
Andrew J Bannister et al.
The Journal of biological chemistry, 280(18), 17732-17736 (2005-03-12)
Methylation of lysine 4 of histone H3 (K4/H3) is linked to transcriptional activity, whereas methylation of K9/H3 is tightly associated with gene inactivity. These are well characterized sites of methylation within histones, but there are numerous other, less characterized, sites
Frank Hirche et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 877(22), 2158-2162 (2009-06-16)
For the investigation of the metabolism and biosynthesis of carnitine, sensitive determination of carnitine and its metabolic precursors, trimethyllysine and gamma-butyrobetaine, is required. We present here a new simplified method for the analysis of carnitine, its acetyl- and propyl esters
Karin Strijbis et al.
IUBMB life, 62(5), 357-362 (2010-03-23)
The water-soluble zwitterion carnitine is an essential metabolite in eukaryotes required for fatty acid oxidation as it functions as a carrier during transfer of activated acyl and acetyl groups across intracellular membranes. Most eukaryotes are able to synthesize carnitine endogenously
C J Rebouche et al.
The Journal of nutrition, 116(5), 751-759 (1986-05-01)
Rates of carnitine biosynthesis in mammals depend on the availability of substrates and the activity of enzymes subserving the pathway. This study was undertaken to test the hypothesis that the availability of epsilon-N-trimethyllysine is rate-limiting for synthesis of carnitine in
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