Compound Identification
SMILES
CC1=CN([C@@H]2O[C@H](CNP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]2O)C(=O)NC1=O
InChIKey
InChIKey=OYUZHGXXSZCYHB-JXOAFFINSA-N
Formula
C10H18N3O14P3
Mass
497.182
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
- Class 5'-deoxyribonucleosides
-
Superclass
Nucleosides, nucleotides, and analogues
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
5'-deoxyribonucleosides
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
5'-deoxyribonucleosides
Alternative Parents
Glycosylamines Pyrimidones Organic phosphoramides Monosaccharides Hydropyrimidines Vinylogous amides Oxolanes Heteroaromatic compounds Ureas Secondary alcohols 1,2-diols Lactams Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Organic oxides Organonitrogen compounds
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
5'-deoxyribonucleoside - Glycosyl compound - N-glycosyl compound - Pyrimidone - Hydropyrimidine - Monosaccharide - Organic phosphoric acid derivative - Pyrimidine - Organic phosphoric acid amide - Heteroaromatic compound - Oxolane - Vinylogous amide - 1,2-diol - Lactam - Urea - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Alcohol - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as 5'-deoxyribonucleosides. These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom. The nucleobases here are limited to purine, pyrimidine, and pyridine derivatives.
External Descriptors
Not available