Structure Information
Structure

Compound Identification

SMILES

CCNC(=O)C1OC(C(O)C1O)N1C=NC2=C1N=CN=C2NC(CC)CC1=CC=CC=C1

InChIKey

InChIKey=VCUQGOSHXYKVAK-UHFFFAOYSA-N

Formula

C22H28N6O4

Mass

440.504

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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-alkylaminopurine - 6-aminopurine - Amphetamine or derivatives - Imidazopyrimidine - Purine - Aminopyrimidine - Secondary aliphatic/aromatic amine - Monocyclic benzene moiety - N-substituted imidazole - Pyrimidine - Imidolactam - Benzenoid - Oxolane - Imidazole - Heteroaromatic compound - Azole - Amino acid or derivatives - Secondary carboxylic acid amide - Secondary alcohol - Carboxamide group - 1,2-diol - Organoheterocyclic compound - Azacycle - Secondary amine - Oxacycle - Carboxylic acid derivative - Alcohol - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic nitrogen compound - 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

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