30312
Nα-Methyl-L-lysine monohydrochloride
≥98.0% (TLC)
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Synonym(s):
(S)-6-Amino-2-(methylamino)hexanoic acid hydrochloride, N-Me-Lys-OH · HCl
Empirical Formula (Hill Notation):
C7H16N2O2 · HCl
CAS Number:
Molecular Weight:
196.68
Beilstein:
6118109
MDL number:
UNSPSC Code:
12352202
PubChem Substance ID:
NACRES:
NA.32
Recommended Products
Quality Level
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.
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Regulatory Information
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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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