Structure Information
Structure

Compound Identification

SMILES

CC(=O)NC1=CC=C(C=C1)C1=CC=C(C=C1)N(C(C)=O)C1=NC2=C(NC(N)=NC2=O)N1[C@H]1C[C@H](O)[C@@H](CO)O1

InChIKey

InChIKey=YIZUHBCLBGXHBM-PWRODBHTSA-N

Formula

C26H27N7O6

Mass

533.545

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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 - 6-oxopurine - Acetanilide - Hypoxanthine - N-acetylarylamine - Imidazopyrimidine - Anilide - Purine - N-arylamide - Aminopyrimidine - Pyrimidone - Monocyclic benzene moiety - N-substituted imidazole - Pyrimidine - Benzenoid - Azole - Heteroaromatic compound - Imidazole - Oxolane - Acetamide - Vinylogous amide - Tertiary carboxylic acid amide - Secondary carboxylic acid amide - Amino acid or derivatives - Secondary alcohol - Carboxamide group - Organoheterocyclic compound - Azacycle - Oxacycle - Carboxylic acid derivative - Primary alcohol - Alcohol - Amine - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Primary amine - Organic oxygen compound - Organonitrogen compound - Organopnictogen compound - Organooxygen compound - 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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