1-Methylcytosine
1-Methylcytosine is a methylated form of the DNA base cytosine.
Names | |
---|---|
Preferred IUPAC name
4-Amino-1-methylpyrimidin-2(1H)-one | |
Identifiers | |
3D model (JSmol) |
|
ChEBI | |
ChEMBL | |
ChemSpider | |
MeSH | 1-Methylcytosine |
PubChem CID |
|
UNII | |
CompTox Dashboard (EPA) |
|
| |
| |
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 |
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.
- Hoshika, Shuichi; et al. (22 February 2019). "Hachimoji DNA and RNA: A genetic system with eight building blocks". Science. 363 (6429): 884–887. doi:10.1126/science.aat0971. PMC 6413494. PMID 30792304.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.