Page last updated: 2024-12-09

alpha-acetyllysine methyl ester

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

alpha-acetyllysine methyl ester: RN refers to the (L-Lys)-isomer [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

N(alpha)-acetyl-L-lysine methyl ester : An alpha-amino acid ester obtained by formal condensation of the carboxy group of N(alpha)-acetyl-L-lysine with the hydroxy group of 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 CID2724394
CHEBI ID64859
SCHEMBL ID2387748
MeSH IDM0190106

Synonyms (21)

Synonym
n.alpha.-acetyl-l-lysine methyl ester
alme
methyl (2s)-2-acetamido-6-aminohexanoate
6072-02-2
alpha-acetyllysine methyl ester
alpha-acetyl-l-lysine methyl ester
l-lysine, n2-acetyl-, methyl ester
n(alpha)-acetyl-l-lysine methyl ester
methyl n-acetyl-l-lysinate
methyl n-acetyl-6-amino-l-norleucinate
CHEBI:64859
methyl n(2)-acetyl-l-lysinate
methyl n(2)-acetyllysinate
SCHEMBL2387748
HHOLXTXLQMKUGJ-QMMMGPOBSA-N
methyl 2-(acetylamino)-6-aminohexanoate #
AKOS030212055
Q27133503
acetyl-l-lysine methyl ester
EN300-24815087
methyl (2s)-6-amino-2-acetamidohexanoate
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (5)

ClassDescription
L-lysine derivativeA proteinogenic amino acid derivative resulting from reaction of L-lysine at the amino group or the carboxy group, or from the replacement of any hydrogen of L-lysine by a heteroatom.
alpha-amino acid esterThe amino acid ester derivative obtained the formal condensation of an alpha-amino acid with an alcohol.
acetamidesCompounds with the general formula RNHC(=O)CH3.
methyl esterAny carboxylic ester resulting from the formal condensation of a carboxy group with methanol.
primary amino compoundA compound formally derived from ammonia by replacing one hydrogen atom by an organyl group.
[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 (3)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's2 (66.67)18.2507
2000's1 (33.33)29.6817
2010's0 (0.00)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: 12.46

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 weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index12.46 (24.57)
Research Supply Index1.79 (2.92)
Research Growth Index4.25 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.46)

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%
Other5 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]