Structure Information
Structure

Compound Identification

SMILES

O[C@H]1C[C@@H](O[C@@H]1COC1(C2=CC=CC=C2)C2=CC=CC=C2SC2=CC=CC=C12)N1C=NC2=C1N=CN=C2NC(=O)C1=CC=CC=C1

InChIKey

InChIKey=MKNSESMLGFJSTR-WTNLLYQRSA-N

Formula

C36H29N5O4S

Mass

627.72

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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 - Thioxanthene - Diarylthioether - Imidazopyrimidine - Benzamide - 1-benzothiopyran - Benzothiopyran - Benzoic acid or derivatives - Purine - Benzylether - Aryl thioether - Benzoyl - N-substituted imidazole - Monocyclic benzene moiety - Pyrimidine - Benzenoid - Imidolactam - Oxolane - Imidazole - Azole - Heteroaromatic compound - Secondary alcohol - Secondary carboxylic acid amide - Carboxamide group - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Dialkyl ether - Ether - Thioether - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Alcohol - Organooxygen 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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