Page last updated: 2024-12-07

l-lysine methyl ester

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Description

L-lysine methyl ester (L-Lys-OMe) is a synthetic derivative of the essential amino acid L-lysine. It is a white, crystalline solid that is soluble in water. The compound is often used as a building block for the synthesis of peptides and other biologically active molecules. It is also being investigated for its potential therapeutic benefits, particularly in the areas of wound healing and immune modulation. Some studies suggest that L-Lys-OMe can enhance wound healing by promoting collagen synthesis and reducing inflammation. It is also being explored for its potential to modulate the immune response, with some research indicating that it can suppress the production of pro-inflammatory cytokines. Further research is ongoing to better understand the mechanisms of action and potential applications of L-Lys-OMe in various fields.'

methyl L-lysinate : The L-lysyl ester formed by conjugating L-lysine with methanol. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID117779
CHEMBL ID1229067
CHEBI ID21354
SCHEMBL ID214894
MeSH IDM0064503

Synonyms (24)

Synonym
l-lysine methylester
methyl lysinate
CHEBI:21354 ,
l-lysine methyl ester
687-64-9
methyl l-lysinate
STK801848
methyl (2s)-2,6-diaminohexanoate
AKOS005622600
CHEMBL1229067
BBL010918
einecs 211-697-8
S11847
SCHEMBL214894
KPNBUPJZFJCCIQ-LURJTMIESA-N
lysine methyl ester
LME ,
methyl (s)-2,6-diaminohexanoate
alpha,epsilon-diaminocaproic methyl ester
13515-95-2
Q27109393
(s)-methyl 2,6-diaminohexanoate
CS-0454891
EN300-7689229
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
L-lysyl esterAn alpha-amino acid ester of L-lysine.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Research

Studies (8)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (12.50)18.7374
1990's1 (12.50)18.2507
2000's2 (25.00)29.6817
2010's4 (50.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 19.13

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index19.13 (24.57)
Research Supply Index2.20 (2.92)
Research Growth Index4.80 (4.65)
Search Engine Demand Index15.26 (26.88)
Search Engine Supply Index3.00 (0.95)

This Compound (19.13)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other8 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]