Compound Identification
SMILES
OC[C@]12CCO[C@H]1[C@@H](O)[C@@H](O2)N1C=NC2=C1N=C(Cl)N=C2Cl
InChIKey
InChIKey=YPXWCLRJUVUBCO-BQIHAETKSA-N
Formula
C12H12Cl2N4O4
Mass
347.15
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
Glycosylamines Purines and purine derivatives Furofurans 2-halopyrimidines Aryl chlorides Monosaccharides N-substituted imidazoles Heteroaromatic compounds Oxolanes Secondary alcohols Azacyclic compounds Dialkyl ethers Oxacyclic compounds Hydrocarbon derivatives Primary alcohols Organochlorides Organonitrogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - Glycosyl compound - N-glycosyl compound - Purine - Imidazopyrimidine - Furofuran - 2-halopyrimidine - Halopyrimidine - Aryl chloride - Aryl halide - N-substituted imidazole - Monosaccharide - Pyrimidine - Oxolane - Imidazole - Heteroaromatic compound - Azole - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Ether - Dialkyl ether - Organochloride - Organonitrogen compound - Organooxygen compound - Primary alcohol - Alcohol - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Organohalogen 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