5-Methylcytidine
Chemical compound
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 | |
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3D model (JSmol) |
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ChemSpider |
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ECHA InfoCard | 100.016.719 |
PubChem CID |
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UNII |
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CompTox Dashboard (EPA) |
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InChI
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Properties | |
Chemical formula | 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). Infobox references |
Chemical compound
5-Methylcytidine is a modified nucleoside derived from 5-methylcytosine. It is found in ribonucleic acids of animal, plant, and bacterial origin.[1]
References
- ^ Dunn, D. B. (1960). "Isolation of 5-methylcytidine from ribonucleic acid". Biochimica et Biophysica Acta. 38: 176–178. doi:10.1016/0006-3002(60)91219-1. PMID 13818675.
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Nucleic acid constituents
- Purine
- Adenine
- Guanine
- Hypoxanthine
- Xanthine
- Purine analogue
- Pyrimidine
- Unnatural base pair (UBP)
Ribonucleoside |
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Deoxyribonucleoside |
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(Nucleoside monophosphate)
Ribonucleotide | |
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Deoxyribonucleotide | |
Cyclic nucleotide |
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