Structure Information
Structure

Compound Identification

SMILES

CCOC1=CC=CC(=C1)C(=O)N[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C=NC2=C1N=CN=C2NCCC1=CNC2=C1C=CC=C2OCC1=CC=CC=C1

InChIKey

InChIKey=LRNQKMDVMSDLQT-GXPCTCNKSA-N

Formula

C36H37N7O6

Mass

663.735

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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 - N-glycosyl compound - 6-alkylaminopurine - Glycosyl compound - 6-aminopurine - 3-alkylindole - Indole or derivatives - Purine - Indole - Imidazopyrimidine - Benzamide - Benzoic acid or derivatives - Phenoxy compound - Phenol ether - Benzoyl - Aminopyrimidine - Alkyl aryl ether - Substituted pyrrole - N-substituted imidazole - Benzenoid - Imidolactam - Monocyclic benzene moiety - Pyrimidine - Azole - Heteroaromatic compound - Imidazole - Pyrrole - Oxolane - Secondary alcohol - Carboxamide group - Secondary carboxylic acid amide - Oxacycle - Azacycle - Carboxylic acid derivative - Ether - Organoheterocyclic compound - Organooxygen compound - Alcohol - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Organic oxygen compound - Organic oxide - Primary alcohol - Amine - 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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