Structure Information
Structure

Compound Identification

SMILES

CCNC(=O)NC1=NC=NC2=C1N=CN2C1OC(COC2=C(C(O)=O)C(F)=CC=C2)C2O[C@@H](OC12)\C=C\C1=CC=CC=C1

InChIKey

InChIKey=PZMKPOCSBHVGNM-DORYNJPLSA-N

Formula

C29H27FN6O7

Mass

590.568

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleosides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Purine nucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine nucleoside - 2-halobenzoic acid or derivatives - Halobenzoic acid or derivatives - 2-halobenzoic acid - Halobenzoic acid - Imidazopyrimidine - Purine - Benzoic acid - Benzoic acid or derivatives - Benzoyl - Phenol ether - Phenoxy compound - Styrene - 1-carboxy-2-haloaromatic compound - Halobenzene - Alkyl aryl ether - Fluorobenzene - Monocyclic benzene moiety - Aryl halide - Aryl fluoride - Imidolactam - Benzenoid - Pyrimidine - N-substituted imidazole - Monosaccharide - Azole - Meta-dioxolane - Oxolane - Heteroaromatic compound - Imidazole - Vinylogous halide - Urea - Acetal - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Carboxylic acid - Ether - Monocarboxylic acid or derivatives - Organooxygen compound - Organic oxygen compound - Carbonyl group - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Organofluoride - Organohalogen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine nucleosides. These are compounds comprising a purine base attached to a ribosyl or deoxyribosyl moiety.

External Descriptors

Not available

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