Structure Information
Structure

Compound Identification

SMILES

COC1=C(OC)C=C(CCNC2=NC=NC3=C2N=CN3[C@@H]2O[C@H](CO)[C@@H](O)[C@H]2NC(=O)C2=CC=C(C=C2)C2=CC=CC=C2)C=C1

InChIKey

InChIKey=WDXVCMUBUIBYPY-UNVYQVKTSA-N

Formula

C33H34N6O6

Mass

610.671

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleosides

Subclass

Purine 2'-deoxyribonucleosides

Intermediate Tree Nodes

Not available

Direct Parent

Purine 2'-deoxyribonucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine 2'-deoxyribonucleoside - Biphenyl - N-glycosyl compound - Glycosyl compound - 6-alkylaminopurine - 6-aminopurine - O-dimethoxybenzene - Dimethoxybenzene - Imidazopyrimidine - Purine - Benzamide - Benzoic acid or derivatives - Phenoxy compound - Phenol ether - Anisole - Methoxybenzene - Benzoyl - Alkyl aryl ether - Aminopyrimidine - Pyrimidine - N-substituted imidazole - Monocyclic benzene moiety - Benzenoid - Imidolactam - Azole - Heteroaromatic compound - Imidazole - Oxolane - Secondary carboxylic acid amide - Secondary alcohol - Carboxamide group - Oxacycle - Azacycle - Organoheterocyclic compound - Ether - Carboxylic acid derivative - Organonitrogen compound - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organooxygen compound - Amine - Primary alcohol - Organic oxygen compound - Organic oxide - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine 2'-deoxyribonucleosides. These are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at position 2.

External Descriptors

Not available

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