Chemistry:1-Methylcytosine
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Short description: Chemical compound
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Preferred IUPAC name
4-Amino-1-methylpyrimidin-2(1H)-one | |
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ChEBI | |
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MeSH | 1-Methylcytosine |
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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). | |
Infobox references | |
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
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
- ↑ Kistenmacher, T. J.; Rossi, M. (1977-12-15). "1-Methylcytosine: a refinement". Acta Crystallographica Section B 33 (12): 3962–3965. doi:10.1107/S0567740877012618. ISSN 0567-7408. Bibcode: 1977AcCrB..33.3962R.
- ↑ Hoshika, Shuichi (22 February 2019). "Hachimoji DNA and RNA: A genetic system with eight building blocks". Science 363 (6429): 884–887. doi:10.1126/science.aat0971. PMID 30792304. Bibcode: 2019Sci...363..884H.
Original source: https://en.wikipedia.org/wiki/1-Methylcytosine.
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