Structure Information
Structure

Compound Identification

SMILES

COC1=CC=CC(=C1)C(=O)N[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C=NC2=C1N=CN=C2NCC1=CC=C(OC)C2=CC=CC=C12

InChIKey

InChIKey=GVQPSKMFKFQAJB-JVUUKAHWSA-N

Formula

C30H30N6O6

Mass

570.606

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