Compound Identification
SMILES
O[C@@H]1[C@@H](CN2CCOCC2)O[C@H]([C@@H]1O)N1C=CC(=O)NC1=O
InChIKey
InChIKey=LZYQLCIKQTYBER-HJQYOEGKSA-N
Formula
C13H19N3O6
Mass
313.31
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 Pentoses Pyrimidones Hydropyrimidines Morpholines Vinylogous amides Heteroaromatic compounds Oxolanes Trialkylamines Lactams Ureas 1,2-diols Secondary alcohols Azacyclic compounds Oxacyclic compounds Dialkyl ethers Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
5'-deoxyribonucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Pyrimidone - Hydropyrimidine - Monosaccharide - Morpholine - Oxazinane - Pyrimidine - Heteroaromatic compound - Oxolane - Vinylogous amide - Urea - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - 1,2-diol - Lactam - Dialkyl ether - Oxacycle - Azacycle - Organoheterocyclic compound - Ether - Hydrocarbon derivative - Alcohol - Organic oxygen compound - Organic nitrogen compound - Amine - Organonitrogen compound - Organooxygen compound - Organic oxide - 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 These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom.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