Structure Information
Structure

Compound Identification

SMILES

COC1=CC=CC(=C1)C(=O)NC1C(O)C(CO)OC1N1C=NC2=C1N=CN=C2NCC1=C(C)C=CC(C)=C1

InChIKey

InChIKey=VVQCNHSFLGPELH-UHFFFAOYSA-N

Formula

C27H30N6O5

Mass

518.574

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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 - 6-alkylaminopurine - N-glycosyl compound - Glycosyl compound - 6-aminopurine - Purine - Imidazopyrimidine - Benzamide - Benzoic acid or derivatives - Phenoxy compound - Phenol ether - P-xylene - Benzoyl - Methoxybenzene - Benzylamine - Anisole - Xylene - Secondary aliphatic/aromatic amine - Alkyl aryl ether - Aminopyrimidine - Monocyclic benzene moiety - Imidolactam - Benzenoid - N-substituted imidazole - Pyrimidine - Imidazole - Oxolane - Azole - Heteroaromatic compound - Amino acid or derivatives - Secondary alcohol - Secondary carboxylic acid amide - Carboxamide group - Secondary amine - Ether - Carboxylic acid derivative - Organoheterocyclic compound - Azacycle - Oxacycle - Organooxygen compound - Organic nitrogen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Amine - Primary alcohol - 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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