1-Methylcytosine
Appearance
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Preferred IUPAC name
4-Amino-1-methylpyrimidin-2(1H)-one | |
Identifiers | |
3D model (JSmol)
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ChEBI | |
ChEMBL | |
ChemSpider | |
MeSH | 1-Methylcytosine |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C5H7N3O | |
Molar mass | 125.131 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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1-Methylcytosine is a methylated form of the DNA base cytosine.
In 1-methylcytosine, a methyl group is attached to the 1st atom in the 6-atom ring. This methyl group distinguishes 1-methylcytosine from cytosine.
History
[edit]Miriam Rossi worked on the refinement of 1-methylcytosine.[1]
1-Methylcytosine is used as a nucleobase of hachimoji DNA, in which it pairs with isoguanine.[2]
References
[edit]- ^ Kistenmacher, T. J.; Rossi, M. (1977-12-15). "1-Methylcytosine: a refinement". Acta Crystallographica Section B. 33 (12): 3962–3965. Bibcode:1977AcCrB..33.3962R. doi:10.1107/S0567740877012618. ISSN 0567-7408.
- ^ Hoshika, Shuichi; et al. (22 February 2019). "Hachimoji DNA and RNA: A genetic system with eight building blocks". Science. 363 (6429): 884–887. Bibcode:2019Sci...363..884H. doi:10.1126/science.aat0971. PMC 6413494. PMID 30792304.