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IUPAC name pyrimidopurin-10(3H)-one | |
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Chemical formula | C8H5N5O |
Molar mass | 187.1582 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Y verify (what is ?) Infobox references |
M1G (pyrimidopurin-10(3H)-one) is a heterocyclic compound which is a by-product of base excision repair (BER) of a specific type of DNA adduct called M1dG. The M1dG adduct in turn is formed by a condensation reaction between guanosine nucleotides in DNA and either malondialdehyde or base propenal. If not repaired, these adducts are mutagenic and carcinogenic.
Malondialdehyde is an end product of lipid peroxidation while base propenal is a result of DNA peroxidation.
M1dG is the major endogenous DNA adduct in humans. M1dG adducts have been detected in cell DNA in liver, leucocytes, pancreas and breast in concentrations of 1-120 per 10 nucleotides. Detection and quantification of M1dG adducts in the body as measured by free M1G is a tool for detecting DNA damage that may lead to cancer. Free M1G is also biomarker for oxidative stress.
References
- ^ Marnett LJ (1999). "Lipid peroxidation-DNA damage by malondialdehyde". Mutat. Res. 424 (1–2): 83–95. doi:10.1016/S0027-5107(99)00010-X. PMID 10064852.
- ^ Seto H, Okuda T, Takesue T, Ikemura T (1983). "Reaction of Malonaldehyde with Nucleic Acid. I. Formation of Fluorescent Pyrimidopurin-10(3H)-one Nucleosides". Bulletin of the Chemical Society of Japan. 56 (6): 1799–1802. doi:10.1246/bcsj.56.1799.
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: CS1 maint: multiple names: authors list (link) - Knutson CG, Akingbade D, Crews BC, Voehler M, Stec DF, Marnett LJ (2007). "Metabolism in vitro and in vivo of the DNA base adduct, M1G". Chem. Res. Toxicol. 20 (3): 550–7. doi:10.1021/tx600334x. PMID 17311424.
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External links
- pyrimido(1,2-a)purin-10(3H)-one at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
- 3-(2'-deoxy-beta-D-erythro-pentofuranosyl)pyrimido(1,2-alpha)purin-10(3H)-one at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
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