Structure Information
Structure

Compound Identification

SMILES

COC1=CC=C(\C=C(/C)C(=O)N[C@@H]2[C@@H](CO)O[C@H](C2O)N2C=NC3=C2N=CN=C3N(C)C)C=C1

InChIKey

InChIKey=BJXDTKDCQFOZOF-WBMRUQKWSA-N

Formula

C23H28N6O5

Mass

468.514

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleosides

Subclass

Purine 3'-deoxyribonucleosides

Intermediate Tree Nodes

Not available

Direct Parent

Purine 3'-deoxyribonucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine 3'-deoxyribonucleoside - Cinnamic acid amide - Cinnamic acid or derivatives - N-glycosyl compound - 6-alkylaminopurine - Glycosyl compound - 6-aminopurine - Pentose monosaccharide - Purine - Imidazopyrimidine - Phenoxy compound - Anisole - Dialkylarylamine - Phenol ether - Methoxybenzene - Alkyl aryl ether - Aminopyrimidine - Pyrimidine - Monosaccharide - Benzenoid - N-substituted imidazole - Imidolactam - Monocyclic benzene moiety - Azole - Heteroaromatic compound - Imidazole - Oxolane - Secondary alcohol - Secondary carboxylic acid amide - Amino acid or derivatives - Tertiary amine - Carboxamide group - Organoheterocyclic compound - Ether - Azacycle - Oxacycle - Carboxylic acid derivative - Amine - Carbonyl group - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Primary alcohol - Organonitrogen compound - Organooxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine 3'-deoxyribonucleosides. These are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at position 3.

External Descriptors

Not available

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