General Information of MET (ID: META00804) |
Name |
7-Methylguanosine
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Synonyms |
Click to Show/Hide Synonyms of This Metabolite
2-Amino-6,9-dihydro-7-methyl-6-oxo-9-beta-D-ribofuranosyl-1H-purinium; 2-Amino-6,9-dihydro-7-methyl-6-oxo-9-beta-delta-ribofuranosyl-1H-purinium; 2-Methylguanosine; G; N(2)-Methylguanosine; N(7)-Methylguanosine; m7g
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Source |
Endogenous;Food
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Structure Type |
Purine nucleosides (Click to Show/Hide the Complete Structure Type Hierarchy)
Nucleosides, nucleotides, and analogues
Purine nucleosides
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PubChem CID |
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HMDB ID |
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Formula |
C11H16N5O5
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Structure |
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3D MOL
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2D MOL
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Click to Show/Hide the Molecular/Functional Data (External Links/Property/Function) of This Metabolite
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DrugBank ID |
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ChEBI ID |
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FooDB ID |
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ChemSpider ID |
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METLIN ID |
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Physicochemical Properties |
Molecular Weight |
298.2752 |
Topological Polar Surface Area |
N.A. |
XlogP |
N.A. |
Complexity |
N.A. |
Heavy Atom Count |
N.A. |
Rotatable Bond Count |
N.A. |
Hydrogen Bond Donor Count |
N.A. |
Hydrogen Bond Acceptor Count |
N.A. |
Function |
7-methylguanosine is an endogenous methylated nucleoside found in human fluids; methylated purine bases are present in higher amounts in tumor-bearing patients compared to healthy controls.DNA hypermethylation is a common finding in malignant cells and has been explored as a therapeutic target for hypomethylating agents. When chemical bonds to DNA, the DNA becomes damaged and proper and complete replication cannot occur to make the normal intended cell. A DNA adduct is an abnormal piece of DNA covalently-bonded to a cancer-causing chemical. This has shown to be the start of a cancerous cell, or carcinogenesis. DNA adducts in scientific experiments are used as bio-markers and as such are themselves measured to reflect quantitatively, for comparison, the amount of cancer in the subject. 7-Methylguanosine is a substrate for purine-nucleoside phosphorylase and Eukaryotic translation initiation factor 4E.
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Regulatory Network
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