| 词条 | 5-Methylcytidine |
| 释义 |
| ImageFile = 5-Methylcytidine.svg | ImageSize = 150px | IUPACName = 1-[(4S,2R,3R,5R)-3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-4-amino-5-methyl-pyrimidin-2-one | OtherNames = m5C |Section1={{Chembox Identifiers | CASNo = 2140-61-6 | CASNo_Ref = {{cascite|correct|CAS}} | PubChem = 92918 | ChemSpiderID = 83877 | SMILES = O=C1/N=C(/N)\\C(=C/N1[C@@H]2O[C@@H]([C@@H](O)[C@H]2O)CO)C | InChI = 1/C10H15N3O5/c1-4-2-13(10(17)12-8(4)11)9-7(16)6(15)5(3-14)18-9/h2,5-7,9,14-16H,3H2,1H3,(H2,11,12,17)/t5-,6-,7-,9-/m1/s1 | InChIKey = ZAYHVCMSTBRABG-JXOAFFINBK | StdInChI = 1S/C10H15N3O5/c1-4-2-13(10(17)12-8(4)11)9-7(16)6(15)5(3-14)18-9/h2,5-7,9,14-16H,3H2,1H3,(H2,11,12,17)/t5-,6-,7-,9-/m1/s1 | StdInChIKey = ZAYHVCMSTBRABG-JXOAFFINSA-N |Section2={{Chembox Properties | C=10 | H=15 | N=3 | O=5 | Appearance = | Density = | MeltingPt = | BoilingPt = | Solubility = |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }}5-Methylcytidine is a modified nucleoside derived from 5-methylcytosine. It is found in ribonucleic acids of animal, plant, and bacterial origin.[1] References1. ^{{cite journal | author = Dunn, D. B. | title = Isolation of 5-methylcytidine from ribonucleic acid | journal = Biochimica et Biophysica Acta | year = 1960 | volume = 38 | pages = 176–178 | doi = 10.1016/0006-3002(60)91219-1 | pmid = 13818675}} {{Nucleobases, nucleosides, and nucleotides}}{{DEFAULTSORT:Methylcytodine, 5-}}{{organic-compound-stub}} 2 : Nucleosides|Pyrimidones |
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