Structure Information
Structure

Compound Identification

SMILES

CC(C)C(=O)NC1=NC(=O)C2=C(N1)N(C=N2)[C@H]1C[C@H](SC(=O)C2=CC=CC=C2)[C@@H](CO)O1

InChIKey

InChIKey=JUHPPAGNTYXGQJ-QLFBSQMISA-N

Formula

C21H23N5O5S

Mass

457.51

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleosides

Subclass

Purine 2',3'-dideoxyribonucleosides

Intermediate Tree Nodes

Not available

Direct Parent

Purine 2',3'-dideoxyribonucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine 2',3'-dideoxyribonucleoside - 2',3'-dideoxy-3'-thionucleoside - 6-oxopurine - Hypoxanthine - Benzoic acid or derivatives - Imidazopyrimidine - Purine - Thiobenzoic acid or derivatives - N-arylamide - Benzoyl - Pyrimidone - Benzenoid - Monocyclic benzene moiety - Pyrimidine - N-substituted imidazole - Heteroaromatic compound - Vinylogous amide - Azole - Imidazole - Oxolane - Carbothioic s-ester - Thiocarboxylic acid ester - Secondary carboxylic acid amide - Carboxamide group - Organoheterocyclic compound - Oxacycle - Azacycle - Sulfenyl compound - Thiocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Alcohol - Primary alcohol - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine 2',3'-dideoxyribonucleosides. These are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at positions 2 and 3.

External Descriptors

Not available

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