Structure Information
Structure

Compound Identification

SMILES

OCC1OC(CC1O)N1C=NC2=C1N=CN=C2NC1C(O)C2=CC=CC=C2C2=CC=CC=C12

InChIKey

InChIKey=FQTJUGDLYVBZHV-UHFFFAOYSA-N

Formula

C24H23N5O4

Mass

445.479

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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 - Hydrophenanthrene - Phenanthrene - 6-alkylaminopurine - 6-aminopurine - Naphthalene - Imidazopyrimidine - Purine - Secondary aliphatic/aromatic amine - Aminopyrimidine - Imidolactam - Benzenoid - Pyrimidine - N-substituted imidazole - Tetrahydrofuran - Heteroaromatic compound - Azole - Imidazole - Secondary alcohol - Oxacycle - Secondary amine - Azacycle - Organoheterocyclic compound - Alcohol - Organopnictogen compound - Organic nitrogen compound - Organonitrogen compound - Organic oxygen compound - Organooxygen compound - Hydrocarbon derivative - Amine - Primary alcohol - 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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