Structure Information
Structure

Compound Identification

SMILES

CC(C)(C)C1NNC(O1)[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2NC1=C(Cl)C=C(F)C=C1

InChIKey

InChIKey=YWXIQSBUHQRBIO-KTHZVYGDSA-N

Formula

C21H25ClFN7O4

Mass

493.92

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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 - 6-aminopurine - Imidazopyrimidine - Purine - Aniline or substituted anilines - Aminopyrimidine - Halobenzene - Fluorobenzene - Chlorobenzene - N-substituted imidazole - Aryl chloride - Aryl fluoride - Aryl halide - Imidolactam - Benzenoid - Pyrimidine - Monocyclic benzene moiety - 1,3,4-oxadiazolidine - Oxolane - Heteroaromatic compound - Imidazole - Azole - 1,2-diol - Secondary alcohol - Alkylhydrazine - Oxacycle - Azacycle - Organoheterocyclic compound - Secondary amine - Organooxygen compound - Organic nitrogen compound - Amine - Alcohol - Organic oxygen compound - Hydrocarbon derivative - Organonitrogen compound - Organofluoride - Organochloride - Organohalogen compound - Hydrazine derivative - 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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