Page last updated: 2024-11-06

glycine methyl ester

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

Description

Glycine methyl ester (GME) is a derivative of the amino acid glycine, where the carboxyl group is esterified with methanol. It is a colorless liquid with a characteristic odor. GME is commonly used as a building block in peptide synthesis and is also a valuable intermediate in organic synthesis. It is a versatile reagent, readily participating in various reactions such as amidation, esterification, and alkylation. GME's importance in research stems from its ability to act as a precursor to other bioactive molecules. For instance, it can be used to synthesize dipeptides and cyclic peptides that exhibit diverse biological activities. Additionally, GME has been investigated for its potential therapeutic applications, including its role in treating neurological disorders and cancer. The study of GME focuses on understanding its synthesis, reactivity, and potential applications in medicine and material science.'

glycine methyl ester: RN given refers to parent cpd [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

methyl glycinate : A glycinyl ester obtained by the formal condensation of the carboxy group of glycine 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]

FloraRankFlora DefinitionFamilyFamily Definition
GlycinegenusA non-essential amino acid. It is found primarily in gelatin and silk fibroin and used therapeutically as a nutrient. It is also a fast inhibitory neurotransmitter.[MeSH]FabaceaeThe large family of plants characterized by pods. Some are edible and some cause LATHYRISM or FAVISM and other forms of poisoning. Other species yield useful materials like gums from ACACIA and various LECTINS like PHYTOHEMAGGLUTININS from PHASEOLUS. Many of them harbor NITROGEN FIXATION bacteria on their roots. Many but not all species of beans belong to this family.[MeSH]

Cross-References

ID SourceID
PubMed CID69221
CHEMBL ID1193103
CHEBI ID87375
MeSH IDM0108968

Synonyms (43)

Synonym
chebi:87375 ,
CHEMBL1193103
glycine, methyl ester
nh2ch2cooch3
methyl 2-aminoacetate
glycine o-methyl ester
methyl aminoacetate
616-34-2
methyl glycine
glycine, methyl ester (6ci,8ci,9ci)
methyl glycinate
methyl glycine ester
(methoxycarbonyl)methylamine
glycine methyl ester
A25962
glycine methylester;2-aminoacetic acid methyl ester;aminoacetic acid methyl;d-glycine methyl ester;glycine methyl;glycine methyl ester
STK739605
einecs 210-477-9
ahx73584r6 ,
unii-ahx73584r6
methyl2-aminoacetate
AKOS005530483
o-methyl-glycine
meu ,
glyome
glycine-methylester
gly-ome
amino-acetic acid methyl ester
aminoacetic acid methyl ester
glycine-methyl ester
h-gly-och3
methyl amino-acetate
h-gly-ome
glycine methylester
methylglycinate
methyl aminoacetate #
DTXSID30210599
aminoacetate methyl ester
FT-0717724
Q27159568
EN300-33965
CS-0454289
E80444

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" However, the LD50 decreased 90-fold when the highest modification was achieved."( Reduction of ricin toxicity without impairing the saccharide-binding properties by chemical modification of the carboxyl groups.
Díaz-Mauriño, T; Solís, D; Vallejo, M, 1993
)
0.29

Bioavailability

ExcerptReferenceRelevance
" Our results suggest that L-valine is a desirable L-amino acid for the esterification of poorly permeable drugs to enhance their oral bioavailability targeting intestinal PEPT1."( Recognition of L-amino acid ester compounds by rat peptide transporters PEPT1 and PEPT2.
Hashimoto, Y; Inui, KI; Saito, H; Sawada, K; Terada, T, 1999
)
0.3
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
metaboliteAny intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
[role 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]

Drug Classes (1)

ClassDescription
glycinyl esterAn alpha-amino acid ester in which the amnio acid component is glycine.
[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 (2)

Assay IDTitleYearJournalArticle
AID678878TP_TRANSPORTER: inhibition of Gly-Sar uptake (Gly-Sar: 20 uM, Gly-OMe: 10000 uM) in PEPT2-expressing LLC-PK1 cells1999The Journal of pharmacology and experimental therapeutics, Nov, Volume: 291, Issue:2
Recognition of L-amino acid ester compounds by rat peptide transporters PEPT1 and PEPT2.
AID679861TP_TRANSPORTER: inhibition of Gly-Sar uptake (Gly-Sar: 20 uM, Gly-OMe: 10000 uM) in PEPT1-expressing LLC-PK1 cells1999The Journal of pharmacology and experimental therapeutics, Nov, Volume: 291, Issue:2
Recognition of L-amino acid ester compounds by rat peptide transporters PEPT1 and PEPT2.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (31)

TimeframeStudies, This Drug (%)All Drugs %
pre-19908 (25.81)18.7374
1990's8 (25.81)18.2507
2000's8 (25.81)29.6817
2010's5 (16.13)24.3611
2020's2 (6.45)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 38.22

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

MetricThis Compound (vs All)
Research Demand Index38.22 (24.57)
Research Supply Index3.53 (2.92)
Research Growth Index4.48 (4.65)
Search Engine Demand Index50.53 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (38.22)

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%
Other33 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]