5-Methyluridine triphosphate
5-Methyluridine triphosphate
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Systematic (IUPAC) name |
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[(2R,3S,5R)-3-hydroxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methyl (hydroxy-phosphonooxyphosphoryl) hydrogen phosphate |
Clinical data |
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Identifiers |
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? N |
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PubChem |
CID 451388 |
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ChemSpider |
397621 N |
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ChEMBL |
CHEMBL607677 N |
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Chemical data |
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Formula |
C10H17N2O15P3 |
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498.2 g/mol |
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SMILES
- CC1=CN(C(=O)NC1=O)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O)O
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InChI=1S/C10H17N2O15P3/c1-4-2-12(10(16)11-8(4)15)9-7(14)6(13)5(25-9)3-24-29(20,21)27-30(22,23)26-28(17,18)19/h2,5-7,9,13-14H,3H2,1H3,(H,20,21)(H,22,23)(H,11,15,16)(H2,17,18,19)/t5-,6-,7-,9-/m1/s1
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Key:RZCIEJXAILMSQK-JXOAFFINSA-N
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5-Methyluridine triphosphate or m5UTP is one of five nucleoside triphosphates. It is the ribonucleoside triphosphate of thymidine, but the nomenclature with "5-methyluridine" is used because the term thymidine triphosphate is used for the deoxyribonucleoside by convention.[1]
References
- ↑ Coghill, Anne M.; Garson, Lorrin R., ed. (2006). The ACS style guide: effective communication of scientific information (3rd ed.). Washington, D.C.: American Chemical Society. p. 244. ISBN 978-0-8412-3999-9.
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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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| Carbohydrates |
- Alcohols
- Glycoproteins
- Glycosides
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| Lipids |
- Eicosanoids
- Fatty acids
- Glycerides
- Phospholipids
- Sphingolipids
- Steroids
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| Nucleic acids | |
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| Proteins | |
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| Other |
- Tetrapyrroles
- intermediates
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