Compound Identification
SMILES
OCC1OC(C(O)C1O)N1C=NC2=C1N=C(I)N=C2NN1CCCCC1
InChIKey
InChIKey=LXHOSGMPFDCRKI-UHFFFAOYSA-N
Formula
C15H21IN6O4
Mass
476.275
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 Pentoses Purines and purine derivatives 2-halopyrimidines Piperidines N-substituted imidazoles Imidolactams Aryl iodides Tetrahydrofurans Heteroaromatic compounds Secondary alcohols Oxacyclic compounds Azacyclic compounds Alkylhydrazines Primary alcohols Organopnictogen compounds Organoiodides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - N-glycosyl compound - Glycosyl compound - Pentose monosaccharide - Purine - Imidazopyrimidine - 2-halopyrimidine - Halopyrimidine - Imidolactam - Pyrimidine - Piperidine - N-substituted imidazole - Monosaccharide - Aryl iodide - Aryl halide - Heteroaromatic compound - Tetrahydrofuran - Imidazole - Azole - Secondary alcohol - Alkylhydrazine - Oxacycle - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Organonitrogen compound - Organoiodide - Organohalogen compound - Hydrazine derivative - Alcohol - 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