Compound Identification
SMILES
CC1(C)O[C@@H]2[C@H](O1)[C@H](O[C@H]2N1C=NC2=C1N=CN=C2N)C(=O)NO
InChIKey
InChIKey=HHUNLHXAOMTCFR-BSFVXNEUSA-N
Formula
C13H16N6O5
Mass
336.308
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 Ketals Aminopyrimidines and derivatives Primary aromatic amines N-substituted imidazoles Imidolactams Oxolanes 1,3-dioxolanes Heteroaromatic compounds Amino acids and derivatives Hydroxamic acids Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Organic oxides Organopnictogen compounds Carbonyl compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - 6-aminopurine - Purine - Imidazopyrimidine - Ketal - Aminopyrimidine - Imidolactam - Pyrimidine - Primary aromatic amine - N-substituted imidazole - Heteroaromatic compound - Imidazole - Oxolane - Meta-dioxolane - Azole - Hydroxamic acid - Amino acid or derivatives - Acetal - Carboxylic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Organic oxygen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Amine - Organopnictogen compound - Primary amine - 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