Compound Identification
SMILES
CCCCCCCCCCCCCCCCCCCC(=O)NC1=NC(=S)N(C=C1)[C@@H]1O[C@H](CO)[C@@H](O)[C@@H]1O
InChIKey
InChIKey=CGBAYSHESKKJRQ-NNTQFHGGSA-N
Formula
C29H51N3O5S
Mass
553.8
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
- Class Pyrimidine nucleosides
-
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 N-arylamides Pyrimidinethiones Imidolactams Hydropyrimidines Fatty amides Oxolanes Heteroaromatic compounds Secondary alcohols 1,2-diols Secondary carboxylic acid amides Oxacyclic compounds Azacyclic compounds Primary alcohols Organosulfur compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Pyrimidine nucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - N-arylamide - Pyrimidinethione - Pyrimidine - Fatty amide - Imidolactam - Monosaccharide - Fatty acyl - Hydropyrimidine - Heteroaromatic compound - Oxolane - Secondary carboxylic acid amide - Carboxamide group - 1,2-diol - Secondary alcohol - Carboxylic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Carbonyl group - Alcohol - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - 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