Structure Information
Structure

Compound Identification

SMILES

OC(=O)C(F)(F)F.COC[C@H]1CCCN1C1=NC2=C(N=CN2[C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C(NCC(C2=CC=CC=C2)C2=CC=CC=C2)=N1

InChIKey

InChIKey=DVBDQVJDPAKKED-SEIWCADGSA-N

Formula

C32H37F3N6O7

Mass

674.678

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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

Not available

Substituents

Purine nucleoside - Diphenylmethane - N-glycosyl compound - Glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Pentose monosaccharide - Imidazopyrimidine - Purine - Dialkylarylamine - Aminopyrimidine - N-substituted imidazole - Monosaccharide - Monocyclic benzene moiety - Imidolactam - Pyrimidine - Benzenoid - Azole - Heteroaromatic compound - Alpha-halocarboxylic acid - Imidazole - Alpha-halocarboxylic acid or derivatives - Pyrrolidine - Oxolane - Secondary alcohol - Oxacycle - Azacycle - Carboxylic acid derivative - Carboxylic acid - Dialkyl ether - Organoheterocyclic compound - Ether - Monocarboxylic acid or derivatives - Organic oxygen compound - Alkyl halide - Alkyl fluoride - Carbonyl group - Alcohol - Organic nitrogen compound - Organic oxide - Amine - Primary alcohol - Organooxygen compound - Organonitrogen compound - Organofluoride - Hydrocarbon derivative - Organohalogen 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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