Compound Identification
SMILES
NC1=NC=NC2=C1N=CN2[C@]1(Cl)O[C@H](C(O)P(=O)=O)[C@@](O)([C@H]1O)P(=O)=O
InChIKey
InChIKey=UUIYRLHXLDXWAN-HAOGJCAUSA-N
Formula
C10H10ClN5O8P2
Mass
425.61
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
6-aminopurines Aminopyrimidines and derivatives Imidolactams N-substituted imidazoles Oxolanes Heteroaromatic compounds Secondary alcohols Chlorohydrins Oxacyclic compounds Azacyclic compounds Organophosphorus compounds Hydrocarbon derivatives Alkyl chlorides Primary amines Organochlorides Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - N-substituted imidazole - Imidolactam - Pyrimidine - Azole - Imidazole - Heteroaromatic compound - Oxolane - Chlorohydrin - Halohydrin - Secondary alcohol - Organoheterocyclic compound - Oxacycle - Azacycle - Alkyl chloride - Organochloride - Organohalogen compound - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Alcohol - Organic nitrogen compound - Organic oxide - Organic oxygen compound - Amine - Alkyl halide - Organophosphorus compound - Primary amine - 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