Structure Information
Structure

Compound Identification

SMILES

CC(C)C(=O)NC1=NC=NC2=C1N=CN2[C@H]1C[C@H](O)[C@@H](COC(=O)OCC2=C3C=CC=CC3=CC3=CC=CC=C23)O1

InChIKey

InChIKey=CDMCEAGJLNEKRH-ISJGIBHGSA-N

Formula

C30H29N5O6

Mass

555.591

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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 - Anthracene - Imidazopyrimidine - Purine - N-arylamide - Carbonic acid diester - N-substituted imidazole - Pyrimidine - Benzenoid - Imidolactam - Heteroaromatic compound - Oxolane - Azole - Imidazole - Secondary carboxylic acid amide - Secondary alcohol - Carboxamide group - Carbonic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Carbonyl group - Organooxygen compound - Alcohol - 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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