| Record Information |
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| Version | 1.0 |
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| Creation Date | 2016-09-30 23:19:18 UTC |
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| Update Date | 2020-05-11 20:41:22 UTC |
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| BMDB ID | BMDB0005923 |
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| Secondary Accession Numbers | |
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| Metabolite Identification |
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| Common Name | N4-Acetylcytidine |
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| Description | N4-Acetylcytidine belongs to the class of organic compounds known as pyrimidine nucleosides. Pyrimidine nucleosides are compounds comprising a pyrimidine base attached to a ribosyl or deoxyribosyl moiety. Based on a literature review a significant number of articles have been published on N4-Acetylcytidine. |
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| Structure | |
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| Synonyms | | Value | Source |
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| 4-Acetyl-1-(beta-D-ribofuranosyl)cytosine | ChEBI | | N-{1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]-2-oxo-1,2-dihydropyrimidin-4-yl}acetamide | ChEBI | | 4-Acetyl-1-(b-D-ribofuranosyl)cytosine | Generator | | 4-Acetyl-1-(β-D-ribofuranosyl)cytosine | Generator | | 4-Acetyl-1-(beta-delta-ribofuranosyl)cytosine | HMDB | | 4-Acetylcytidine | HMDB | | N-4-Acetylcytidine | HMDB | | N-Acetyl-cytidine | HMDB | | N-Acetylcytidine | HMDB | | Acetylcytidine | MeSH, HMDB |
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| Chemical Formula | C11H15N3O6 |
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| Average Molecular Weight | 285.2533 |
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| Monoisotopic Molecular Weight | 285.096085227 |
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| IUPAC Name | N-{1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-2-oxo-1,2-dihydropyrimidin-4-yl}acetamide |
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| Traditional Name | N4-acetylcytidine |
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| CAS Registry Number | 3768-18-1 |
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| SMILES | CC(=O)NC1=NC(=O)N(C=C1)[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O |
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| InChI Identifier | InChI=1S/C11H15N3O6/c1-5(16)12-7-2-3-14(11(19)13-7)10-9(18)8(17)6(4-15)20-10/h2-3,6,8-10,15,17-18H,4H2,1H3,(H,12,13,16,19)/t6-,8-,9-,10-/m1/s1 |
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| InChI Key | NIDVTARKFBZMOT-PEBGCTIMSA-N |
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| Chemical Taxonomy |
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| Description | belongs to the class of organic compounds known as pyrimidine nucleosides. Pyrimidine nucleosides are compounds comprising a pyrimidine base attached to a ribosyl or deoxyribosyl moiety. |
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| Kingdom | Organic compounds |
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| Super Class | Nucleosides, nucleotides, and analogues |
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| Class | Pyrimidine nucleosides |
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| Sub Class | Not Available |
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| Direct Parent | Pyrimidine nucleosides |
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| Alternative Parents | |
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| Substituents | - Pyrimidine nucleoside
- Glycosyl compound
- N-glycosyl compound
- Pentose monosaccharide
- Pyrimidone
- Hydropyrimidine
- Monosaccharide
- Pyrimidine
- Tetrahydrofuran
- Heteroaromatic compound
- Secondary alcohol
- Organoheterocyclic compound
- Organic 1,3-dipolar compound
- Propargyl-type 1,3-dipolar organic compound
- Carboximidic acid
- Oxacycle
- Azacycle
- Carboximidic acid derivative
- Hydrocarbon derivative
- Organooxygen compound
- Organonitrogen compound
- Alcohol
- Organic oxygen compound
- Organic nitrogen compound
- Organopnictogen compound
- Primary alcohol
- Organic oxide
- Aromatic heteromonocyclic compound
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| Molecular Framework | Aromatic heteromonocyclic compounds |
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| External Descriptors | |
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| Ontology |
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| Status | Expected but not Quantified |
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| Origin | |
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| Biofunction | Not Available |
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| Application | Not Available |
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| Cellular locations | Not Available |
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| Physical Properties |
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| State | Solid |
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| Experimental Properties | | Property | Value | Reference |
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| Melting Point | Not Available | Not Available | | Boiling Point | Not Available | Not Available | | Water Solubility | Not Available | Not Available | | LogP | Not Available | Not Available |
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| Predicted Properties | |
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| Spectra |
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| Spectra | |
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