Compound Identification
SMILES
CC1(C)O[C@@H]2[C@H](O1)[C@H](O[C@H]2N1C=NC2=C1N=CN=C2Cl)C(O)=O
InChIKey
InChIKey=BWQOSYSWEARUOW-MCHASIABSA-N
Formula
C13H13ClN4O5
Mass
340.72
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
Purines and purine derivatives Halopyrimidines Ketals Aryl chlorides N-substituted imidazoles Oxolanes 1,3-dioxolanes Heteroaromatic compounds Oxacyclic compounds Azacyclic compounds Carboxylic acids Monocarboxylic acids and derivatives Organonitrogen compounds Organopnictogen compounds Organochlorides Hydrocarbon derivatives Organic oxides Carbonyl compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - Imidazopyrimidine - Purine - Ketal - Halopyrimidine - Aryl chloride - Aryl halide - N-substituted imidazole - Pyrimidine - Meta-dioxolane - Azole - Heteroaromatic compound - Imidazole - Oxolane - Acetal - Carboxylic acid derivative - Carboxylic acid - Oxacycle - Azacycle - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Organopnictogen compound - Organic oxide - Carbonyl group - Organohalogen compound - Organochloride - Organonitrogen compound - Organooxygen 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