Compound Identification
SMILES
CCNC(=O)[C@H]1O[C@H]([C@@H]2OC(C)(C)O[C@H]12)N1C=NC2=C(C)N=C(Cl)N=C12
InChIKey
InChIKey=LJGFNPGLSMCWGE-FBKDDSFISA-N
Formula
C16H20ClN5O4
Mass
381.82
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 2-halopyrimidines Ketals Aryl chlorides N-substituted imidazoles Oxolanes 1,3-dioxolanes Heteroaromatic compounds Secondary carboxylic acid amides Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Carbonyl compounds Organic oxides Organochlorides Organonitrogen compounds Organopnictogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - Purine - Imidazopyrimidine - Halopyrimidine - Ketal - 2-halopyrimidine - N-substituted imidazole - Aryl halide - Pyrimidine - Aryl chloride - Heteroaromatic compound - Imidazole - Azole - Oxolane - Meta-dioxolane - Carboxamide group - Secondary carboxylic acid amide - Acetal - Carboxylic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organopnictogen compound - Organooxygen compound - Organohalogen compound - Organochloride - Organonitrogen 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