Compound Identification
SMILES
CNCC1=CN([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C(=S)NC1=O
InChIKey
InChIKey=HXVKEKIORVUWDR-FDDDBJFASA-N
Formula
C11H17N3O5S
Mass
303.33
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
- Class Pyrimidine nucleosides
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Superclass
Nucleosides, nucleotides, and analogues
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Pyrimidine nucleosides
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Pyrimidine nucleosides
Alternative Parents
Glycosylamines Pentoses Pyrimidones Pyrimidinethiones 2-Thiopyrimidines Aralkylamines Hydropyrimidines Vinylogous amides Oxolanes Heteroaromatic compounds Thioureas Secondary alcohols Lactams Oxacyclic compounds Azacyclic compounds Dialkylamines Hydrocarbon derivatives Organic oxides Primary alcohols
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Pyrimidine nucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - 2-thiopyrimidine - Thiopyrimidine - Pyrimidinethione - Pyrimidone - Aralkylamine - Hydropyrimidine - Monosaccharide - Pyrimidine - Heteroaromatic compound - Vinylogous amide - Oxolane - Thiourea - Secondary alcohol - Lactam - Secondary amine - Oxacycle - Azacycle - Organoheterocyclic compound - Secondary aliphatic amine - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Amine - Organosulfur compound - Alcohol - Organic oxygen compound - Organic nitrogen compound - Organic oxide - Primary alcohol - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as pyrimidine nucleosides. These are compounds comprising a pyrimidine base attached to a ribosyl or deoxyribosyl moiety.
External Descriptors
Not available