Compound Identification
SMILES
CC1(C)O[C@@H]2[C@H](CO)O[C@@H]([C@H]2O1)N1C=NC2=C1NC(=O)NC2=O
InChIKey
InChIKey=NTPNWZDFSVOISL-YRCUVVFSSA-N
Formula
C13H16N4O6
Mass
324.293
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
- Class Purine nucleosides
-
Superclass
Nucleosides, nucleotides, and analogues
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Purine nucleosides
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Purine nucleosides
Alternative Parents
Xanthines 6-oxopurines Alkaloids and derivatives Pyrimidones Ketals N-substituted imidazoles Monosaccharides Vinylogous amides 1,3-dioxolanes Oxolanes Heteroaromatic compounds Ureas Lactams Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Organic oxides Organonitrogen compounds Organopnictogen compounds Primary alcohols
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - Xanthine - 6-oxopurine - Purinone - Purine - Imidazopyrimidine - Alkaloid or derivatives - Ketal - Pyrimidone - Pyrimidine - Monosaccharide - N-substituted imidazole - Azole - Heteroaromatic compound - Imidazole - Vinylogous amide - Oxolane - Meta-dioxolane - Lactam - Urea - Organoheterocyclic compound - Azacycle - Oxacycle - Acetal - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Alcohol - Primary alcohol - Organic oxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as purine nucleosides. These are compounds comprising a purine base attached to a ribosyl or deoxyribosyl moiety.
External Descriptors
Not available