Structure Information
Structure

Compound Identification

SMILES

CC(=O)NC1=CC=C(C=C1)C1=CC=C(NC2=NC3=C(NC(N)=NC3=O)N2[C@H]2C[C@H](O)[C@@H](CO)O2)C=C1

InChIKey

InChIKey=BJJUQBWYLRXWNN-IPMKNSEASA-N

Formula

C24H25N7O5

Mass

491.508

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