Structure Information
Structure

Compound Identification

SMILES

COC1=C(OC)C=C(CCNC2=NC=NC3=C2N=CN3[C@@H]2O[C@H](CO)[C@@H](O)[C@H]2NC(=O)C2=CC3=C(NC=C3)C=C2)C=C1

InChIKey

InChIKey=LYULKWJIJACHKG-BYHVZLFPSA-N

Formula

C29H31N7O6

Mass

573.61

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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 - Indolecarboxylic acid derivative - Indolecarboxamide derivative - 6-alkylaminopurine - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Dimethoxybenzene - O-dimethoxybenzene - Indole or derivatives - Purine - Indole - Imidazopyrimidine - Anisole - Phenol ether - Phenoxy compound - Methoxybenzene - Aminopyrimidine - Alkyl aryl ether - Benzenoid - N-substituted imidazole - Pyrimidine - Imidolactam - Monocyclic benzene moiety - Azole - Heteroaromatic compound - Imidazole - Pyrrole - Oxolane - Secondary alcohol - Secondary carboxylic acid amide - Carboxamide group - Organoheterocyclic compound - Carboxylic acid derivative - Ether - Oxacycle - Azacycle - Organooxygen compound - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Organic oxide - Primary alcohol - Amine - Organic oxygen 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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