Structure Information
Structure

Compound Identification

SMILES

CC1(C)C2CC1C(CC2)C(=O)CCOC1=NC2=C(N=CN2C2O[C@@H](CO)[C@H](O)[C@@H]2O)C(N)=N1

InChIKey

InChIKey=FTDMBMYJUDDWSO-SQMXWIIPSA-N

Formula

C22H31N5O6

Mass

461.519

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Taxonomic Classification

Taxonomy Tree

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

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Aromatic monoterpenoid - Monoterpenoid - Nopinane monoterpenoid - Pinane monoterpenoid - Pentose monosaccharide - Imidazopyrimidine - Purine - Alkyl aryl ether - Aminopyrimidine - N-substituted imidazole - Monosaccharide - Imidolactam - Pyrimidine - Oxolane - Azole - Heteroaromatic compound - Imidazole - 1,2-diol - Secondary alcohol - Ketone - Organoheterocyclic compound - Ether - Azacycle - Oxacycle - Primary alcohol - Primary amine - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Amine - Organic oxygen compound - Alcohol - Organooxygen compound - 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

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