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Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](CO)C[C@H]1O.OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1NC=NC[C@H]2O

InChIKey

InChIKey=LTKCTRYZMGHRNR-VKMGIUIFSA-N

Formula

C21H29N9O8

Mass

535.518

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleosides

Subclass

Purine 3'-deoxyribonucleosides

Intermediate Tree Nodes

Not available

Direct Parent

Purine 3'-deoxyribonucleosides

Alternative Parents

Molecular Framework

Not available

Substituents

Purine 3'-deoxyribonucleoside - N-glycosyl compound - Glycosyl compound - Imidazodiazepine - Imidazo-meta-diazepine - 6-aminopurine - Purine - Imidazopyrimidine - Meta-diazepine - Aminopyrimidine - Imidolactam - Monosaccharide - N-substituted imidazole - Pyrimidine - Oxolane - Imidazole - Azole - Heteroaromatic compound - Secondary alcohol - 1,2-diol - Formamidine - Amidine - Oxacycle - Carboxylic acid amidine - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Alcohol - Organic oxygen compound - Organic nitrogen compound - Amine - Hydrocarbon derivative - Primary amine - Primary alcohol - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine 3'-deoxyribonucleosides. These are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at position 3.

External Descriptors

Not available

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