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Key Documents

Altri documenti

04685

Sigma-Aldrich

Nε-Methyl-L-lysine hydrochloride

≥98.0% (TLC)

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About This Item

Formula empirica (notazione di Hill):
C7H16N2O2 · HCl
Numero CAS:
7622-29-9
Peso molecolare:
196.68
Numero CE:
231-539-1
Numero MDL:
MFCD00012621
Codice UNSPSC:
12352202
ID PubChem:
329747972
NACRES:
NA.32

Livello qualitativo

100

Saggio

≥98.0% (TLC)

Attività ottica

[α]/D 20.5±1.5°, c = 0.1 in 1 M HCl

Temperatura di conservazione

2-8°C

Stringa SMILE

Cl.CNCCCC[C@H](N)C(O)=O

InChI

1S/C7H16N2O2.ClH/c1-9-5-3-2-4-6(8)7(10)11;/h6,9H,2-5,8H2,1H3,(H,10,11);1H/t6-;/m0./s1
AQELUQTVJOFFBN-RGMNGODLSA-N

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Azioni biochim/fisiol

N ε-methyl-L-lysine was identified as a lysine analog with inhibitory effects on the growth and sporulation of Penicillium chrysogenum and benzyl-penicillin formation by mycelia.

Confezionamento

Bottomless glass bottle. Contents are inside inserted fused cone.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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L-Lysine methyl ester dihydrochloride

Sigma-Aldrich

L0645

L-Lysine methyl ester dihydrochloride

L-Lysine hydrochloride natural, FG

Sigma-Aldrich

W384712

L-Lysine hydrochloride

NHS Act Sepharose™ 4 Fast Flow Cytiva 17-0906-01, pack of 25 mL

GE17-0906-01

NHS Act Sepharose™ 4 Fast Flow

L-lisina from non-animal source, meets EP, JP, USP testing specifications, suitable for cell culture, 98.5-101.0%

Sigma-Aldrich

L8662

L-lisina

L-lisina analytical standard

Supelco

23128

L-lisina

L-lisina reagent grade, ≥98% (HPLC)

Sigma-Aldrich

L5626

L-lisina

F Zappacosta et al.
European journal of biochemistry, 222(3), 761-767 (1994-06-15)
Advanced mass spectrometric procedures have been extensively used to provide an accurate structural characterization of aspartate aminotransferase from Sulfolobus solfataricus. The amino acid sequence of this enzyme had previously been deduced from the DNA sequence. The accurate molecular mass of
H Kalász et al.
Journal of chromatographic science, 43(4), 165-168 (2005-06-25)
Administration of (14)C-labelled L-deprenyl to rats results in the urinary elimination of a 14C-labelled compound. The 9-fluorenylmethoxycarbonyl chloride-reacted urine sample is fractionated by high-performance liquid chromatography (HPLC) on an octadecyl silica stationary phase. N(epsilon)-Monomethyl-lysine is identified in the fraction containing
M Moracci et al.
Enzyme and microbial technology, 17(11), 992-997 (1995-11-01)
The gene coding for the beta-glycosidase from the archaeon Sulfolobus solfataricus has been overexpressed in Escherichia coli. The enzyme was purified to homogeneity with a rapid purification procedure employing a thermal precipitation as a crucial step. The final yield was
H Kalász et al.
Journal of chromatography. A, 1079(1-2), 208-212 (2005-07-26)
Nepsilon-Monomethyllysine was identified in the serum, urine, brain, and liver samples of rats treated per os with L-deprenyl. The identification procedure included reaction with Fmoc chloride, clean-up, and analysis using HPLC-UV-MS. Oral administration of (-)-N-14C-methyl-N-propynyl(2-phenyl-1-methyl)ethylammonium hydrochloride L-deprenyl) to rats resulted
M Kushiro et al.
Nephron, 79(4), 458-468 (1998-08-05)
Increases in extracellular matrix (ECM) and changes in its components have been documented in the glomeruli of diabetic nephropathy. Advanced glycation end products formed by glycoxidation have been shown to induce the synthesis of ECM components and transforming growth factor
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