Names | |
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IUPAC name
5-Methylcytidine | |
Systematic IUPAC name
4-Amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methylpyrimidin-2(1H)-one | |
Other names
m5C | |
Identifiers | |
3D model (JSmol) |
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ChemSpider | |
ECHA InfoCard | 100.016.719 |
PubChem CID |
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UNII | |
CompTox Dashboard (EPA) |
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Properties | |
C10H15N3O5 | |
Molar mass | 257.246 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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5-Methylcytidine is a modified nucleoside derived from 5-methylcytosine. It is found in ribonucleic acids of animal, plant, and bacterial origin.[1]
Nucleic acid constituents
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Nucleobase |
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Nucleoside |
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Nucleotide (Nucleoside monophosphate) |
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Nucleoside diphosphate |
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Nucleoside triphosphate |
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