Structure Information
Structure

Compound Identification

SMILES

OC[C@@H]1C[C@@H](O)[C@@H](O1)N1C=NC2=C1N=CN=C2NC1CCN(C1)C(=O)C1=CC(F)=CC=C1

InChIKey

InChIKey=BKTHVDXBRSAQQK-YGNZUQDKSA-N

Formula

C21H23FN6O4

Mass

442.451

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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

Aromatic heteropolycyclic compounds

Substituents

Purine 3'-deoxyribonucleoside - 6-alkylaminopurine - 6-aminopurine - 3-halobenzoic acid or derivatives - Halobenzoic acid or derivatives - Benzamide - Benzoic acid or derivatives - Imidazopyrimidine - Purine - Benzoyl - N-acylpyrrolidine - Fluorobenzene - Halobenzene - Aminopyrimidine - Monocyclic benzene moiety - N-substituted imidazole - Aryl halide - Aryl fluoride - Imidolactam - Benzenoid - Pyrimidine - Imidazole - Tertiary carboxylic acid amide - Oxolane - Heteroaromatic compound - Azole - Pyrrolidine - Carboxamide group - Secondary alcohol - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Oxacycle - Primary alcohol - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Organic oxygen compound - Alcohol - Organohalogen compound - Organofluoride - Organonitrogen compound - Amine - Organooxygen 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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