Page last updated: 2024-11-06

glutamic acid dimethyl ester

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

Description

Glutamic acid dimethyl ester is a derivative of glutamic acid, an important amino acid involved in neurotransmission and metabolism. The dimethyl ester form is synthesized by esterification of the carboxyl groups of glutamic acid with methanol. This modification alters the compound's properties, making it more soluble in organic solvents and potentially increasing its bioavailability. Glutamic acid dimethyl ester has been investigated for its potential applications in various fields. For instance, it has been studied as a potential building block for the synthesis of peptides and other biologically active molecules. Furthermore, research has explored its potential use in drug delivery systems and as a precursor for the production of biodegradable polymers. The interest in glutamic acid dimethyl ester stems from its unique chemical structure and its potential for diverse applications in medicine, materials science, and other fields. Further research is needed to fully understand its properties and potential applications.'

glutamic acid dimethyl ester: RN given refers to (L)-isomer [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID93032
CHEMBL ID1229075
CHEBI ID184065
SCHEMBL ID131050
MeSH IDM0109663

Synonyms (29)

Synonym
dimethyl glutamate
l-glutamic acid dimethyl ester
6525-53-7
dimethyl l-glutamate
dimethyl (2s)-2-aminopentanedioate
CHEBI:184065
l-glutamic acid, dimethyl ester
unii-3k9bk9lb73
3k9bk9lb73 ,
einecs 229-414-1
glutamic acid dimethyl ester
(s)-dimethyl 2-aminopentanedioate
CHEMBL1229075
SCHEMBL131050
l-glutamic acid dimethylester
J-502486
l-glutamic acid, 1,5-dimethyl ester
glutamic acid, dimethyl ester, l-
(s)-glutamic acid dimethyl ester
dimethyl 2-aminopentanedioate #
DTXSID40215570
(s)-dimethyl2-aminopentanedioate
CS-0094331
Q27257398
AKOS016844376
A850031
EN300-172754
1,5-dimethyl (2s)-2-aminopentanedioate
HY-W037817
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
glutamic acid derivativeAn amino acid derivative resulting from reaction of glutamic acid at the amino group or either of the carboxy groups, or from the replacement of any hydrogen by a heteroatom. The definition normally excludes peptides containing glutamic acid residues.
[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]

Bioassays (7)

Assay IDTitleYearJournalArticle
AID724508Antimicrobial activity against methicillin-sensitive Staphylococcus aureus isolate 309-12013Bioorganic & medicinal chemistry letters, Feb-01, Volume: 23, Issue:3
Synthesis and evaluation of novel sulfenamides as novel anti Methicillin-resistant Staphylococcus aureus agents.
AID724315Antimicrobial activity against methicillin-resistant Staphylococcus aureus isolate 6-422013Bioorganic & medicinal chemistry letters, Feb-01, Volume: 23, Issue:3
Synthesis and evaluation of novel sulfenamides as novel anti Methicillin-resistant Staphylococcus aureus agents.
AID724313Antimicrobial activity against methicillin-resistant Staphylococcus aureus isolate 309-82013Bioorganic & medicinal chemistry letters, Feb-01, Volume: 23, Issue:3
Synthesis and evaluation of novel sulfenamides as novel anti Methicillin-resistant Staphylococcus aureus agents.
AID724316Antimicrobial activity against methicillin-resistant Staphylococcus aureus isolate 309-42013Bioorganic & medicinal chemistry letters, Feb-01, Volume: 23, Issue:3
Synthesis and evaluation of novel sulfenamides as novel anti Methicillin-resistant Staphylococcus aureus agents.
AID724317Antimicrobial activity against methicillin-resistant Staphylococcus aureus isolate Chaoyang2013Bioorganic & medicinal chemistry letters, Feb-01, Volume: 23, Issue:3
Synthesis and evaluation of novel sulfenamides as novel anti Methicillin-resistant Staphylococcus aureus agents.
AID724314Antimicrobial activity against methicillin-resistant Staphylococcus aureus isolate 309-72013Bioorganic & medicinal chemistry letters, Feb-01, Volume: 23, Issue:3
Synthesis and evaluation of novel sulfenamides as novel anti Methicillin-resistant Staphylococcus aureus agents.
AID724510Antimicrobial activity against Staphylococcus aureus ATCC 65382013Bioorganic & medicinal chemistry letters, Feb-01, Volume: 23, Issue:3
Synthesis and evaluation of novel sulfenamides as novel anti Methicillin-resistant Staphylococcus aureus agents.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (21)

TimeframeStudies, This Drug (%)All Drugs %
pre-19903 (14.29)18.7374
1990's9 (42.86)18.2507
2000's5 (23.81)29.6817
2010's3 (14.29)24.3611
2020's1 (4.76)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 18.29

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 Index18.29 (24.57)
Research Supply Index3.09 (2.92)
Research Growth Index4.75 (4.65)
Search Engine Demand Index10.37 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (18.29)

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%
Other21 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]