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30312

Sigma-Aldrich

Nα-Methyl-L-lysine monohydrochloride

≥98.0% (TLC)

Synonym(s):

(S)-6-Amino-2-(methylamino)hexanoic acid hydrochloride, N-Me-Lys-OH · HCl

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100 MG
£240.00
500 MG
£887.00

£240.00

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100 MG
£240.00
500 MG
£887.00

About This Item

Empirical Formula (Hill Notation):
C7H16N2O2 · HCl
CAS Number:
14000-28-3
Molecular Weight:
196.68
Beilstein:
6118109
MDL number:
MFCD00672351
UNSPSC Code:
12352202
PubChem Substance ID:
329753458
NACRES:
NA.32

£240.00

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Quality Level

100

Assay

≥98.0% (TLC)

optical activity

[α]/D 27.5±1.5°, c = 0.1 in 1 M HCl

SMILES string

Cl.CN[C@@H](CCCCN)C(O)=O

InChI

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

InChI key

LWUKQYOOMILVOV-RGMNGODLSA-N

Biochem/physiol Actions

Nα-Methyl-L-lysine was shown to inhibit the growth and sporulation of Penicillium chrysogenum. [1]

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H319

Precautionary Statements

P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM5241
BCBD6428V
BCBC1878V
BCBC1878

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C G Friedrich et al.
Applied and environmental microbiology, 34(6), 706-709 (1977-12-01)
Compounds structurally related to lysine were tested against Penicillium chrysogenum Wis. 54-1255 for inhibition of growth, sporulation, and penicillin formation. This strain is relatively resistant to lysine analogs. The compounds that were the more active inhibitors of growth and whose
D J Gordon et al.
Biochemistry, 40(28), 8237-8245 (2001-07-11)
A potential goal in the prevention or therapy of Alzheimer's disease is to decrease or eliminate neuritic plaques composed of fibrillar beta-amyloid (Abeta). In this paper we describe N-methyl amino acid containing congeners of the hydrophobic "core domain" of Abeta

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