Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1O[C@H]([C@H](OCCCNC(=O)C(F)(F)F)[C@@H]1O)N1C=NC2=C1N=CN=C2N(C(=O)C1=CC=CC=C1)C(=O)C1=CC=CC=C1

InChIKey

InChIKey=HMTRCGCANMHWNS-BMWKMAGWSA-N

Formula

C29H27F3N6O7

Mass

628.565

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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 - N-glycosyl compound - Glycosyl compound - Imidazopyrimidine - Benzoic acid or derivatives - Purine - Benzoyl - Monocyclic benzene moiety - N-substituted imidazole - Pyrimidine - Monosaccharide - Carboxylic acid imide, n-substituted - Imidolactam - Benzenoid - Azole - Heteroaromatic compound - Imidazole - Oxolane - Carboxylic acid imide - Secondary alcohol - Secondary carboxylic acid amide - Carboxamide group - Oxacycle - Carboxylic acid derivative - Azacycle - Dialkyl ether - Ether - Organoheterocyclic compound - Organic nitrogen compound - Alkyl halide - Alkyl fluoride - Alcohol - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Primary alcohol - Organooxygen compound - Organonitrogen compound - Organofluoride - 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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