5-Methylcytosine
| Names | |
|---|---|
| Preferred IUPAC name
4-Amino-5-methylpyrimidin-2(1H)-one | |
| Identifiers | |
3D model (JSmol) |
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| 120387 | |
| ChEBI | |
| ChemSpider | |
| ECHA InfoCard | 100.008.236 |
| EC Number |
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| KEGG | |
| MeSH | 5-Methylcytosine |
PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C5H7N3O | |
| Molar mass | 125.131 g·mol−1 |
| Hazards | |
| GHS labelling: | |
| Warning | |
| H317, H319 | |
| P261, P264, P272, P280, P302+P352, P305+P351+P338, P321, P333+P313, P337+P313, P363, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |
5-Methylcytosine (5mC) is a methylated form of the DNA base cytosine (C) that regulates gene transcription and takes several other biological roles. When cytosine is methylated, the DNA maintains the same sequence, but the expression of methylated genes can be altered (the study of this is part of the field of epigenetics). 5-Methylcytosine is incorporated in the nucleoside 5-methylcytidine.