Page last updated: 2024-12-07

1-methylguanosine

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

Description

1-Methylguanosine (m1G) is a naturally occurring nucleoside, a derivative of guanosine with a methyl group attached to the N1 position of the guanine base. It is found in various biological molecules, including RNA, DNA, and tRNA. m1G plays a role in regulating gene expression and other cellular processes. In tRNA, m1G is critical for maintaining the correct structure and function of the molecule, influencing the efficiency of protein synthesis. The synthesis of m1G is catalyzed by specific methyltransferases, which transfer a methyl group from S-adenosyl methionine to the guanine base. Researchers study m1G to understand its roles in various cellular processes, including gene expression, RNA splicing, and protein synthesis. m1G has also been implicated in certain diseases, such as cancer. Understanding the function and regulation of m1G could lead to the development of new therapies for these diseases.'

1-methylguanosine : Guanosine substituted with a methyl group at position N-1. [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 CID96373
CHEMBL ID3246759
CHEBI ID19062
SCHEMBL ID62505
MeSH IDM0074862

Synonyms (22)

Synonym
2-amino-9-[(2r,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1-methyl-6,9-dihydro-1h-purin-6-one
2140-65-0
n1-methylguanosine
1-methylguanosine
2-amino-9-[(2r,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]-1-methyl-1,9-dihydro-6h-purin-6-one
CHEBI:19062 ,
2-amino-9-[(2r,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1-methylpurin-6-one
nsc 70897
CHEMBL3246759 ,
SCHEMBL62505
1-methyl-guanosine
trmd protein
J-014033
CS-0061836
HY-113136
AKOS030573954
2-amino-9-((2r,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-1-methyl-1h-purin-6(9h)-one
bdbm50557953
Q27109106
2-azanyl-9-[(2r,3r,4s,5r)-5-(hydroxymethyl)-3,4-bis(oxidanyl)oxolan-2-yl]-1-methyl-purin-6-one
DTXSID901316493
AS-77299
[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
methylguanosineAny guanosine carrying one or more methyl substituents.
[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]

Protein Targets (1)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (4)

Assay IDTitleYearJournalArticle
AID1136399Activity of human erythrocyte purine nucleoside phosphorylase assessed as ribose relase at 5 umol after 30 mins by orcinol reaction relative to guanosine1978Journal of medicinal chemistry, Sep, Volume: 21, Issue:9
Stereoelectronic factors in the binding of substrate analogues and inhibitors to purine nucleoside phosphorylase isolated from human erythrocytes.
AID1710678Metabolic stability in human intestinal S9 fraction assessed as parent compound remaining at 33 uM incubated for 2 hrs by LC/MS/MS analysis2020RSC medicinal chemistry, Dec-17, Volume: 11, Issue:12
A benzoxazole derivative as an inhibitor of anaerobic choline metabolism by human gut microbiota.
AID1710669Inhibition of CutC in Escherichia coli MS 200-1 assessed as reduction in d9-TMA formation using d9-choline chloride as substrate incubated for 4 hrs under anaerobic condition by LC-MS-MS analysis2020RSC medicinal chemistry, Dec-17, Volume: 11, Issue:12
A benzoxazole derivative as an inhibitor of anaerobic choline metabolism by human gut microbiota.
AID1710670Inhibition of N-terminal His6-tagged Desulfovibrio desulfuricans G20 CutC encoding 52 residues assessed as reduction in acetaldehyde using choline as substrate in presence of NADH-dependent yeast alcohol dehydrogenase by UV-Vis absorbance based assay2020RSC medicinal chemistry, Dec-17, Volume: 11, Issue:12
A benzoxazole derivative as an inhibitor of anaerobic choline metabolism by human gut microbiota.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (36)

TimeframeStudies, This Drug (%)All Drugs %
pre-199013 (36.11)18.7374
1990's10 (27.78)18.2507
2000's3 (8.33)29.6817
2010's8 (22.22)24.3611
2020's2 (5.56)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 22.63

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 Index22.63 (24.57)
Research Supply Index3.66 (2.92)
Research Growth Index4.65 (4.65)
Search Engine Demand Index23.28 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (22.63)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (2.63%)6.00%
Case Studies1 (2.63%)4.05%
Observational0 (0.00%)0.25%
Other36 (94.74%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]