Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCCCCCCCCCCCOC(COC[C@@H]1CC[C@@H](O1)N1C=NC2=C1NC=NC2=O)COC[C@H]1O[C@H](C[C@@H]1N=[N+]=[N-])N1C=C(C)C(=O)NC1=O

InChIKey

InChIKey=WMXOMWKYPOZJRO-OSUUMQKUSA-N

Formula

C41H65N9O8

Mass

812.026

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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 - Pyrimidine 2',3'-dideoxyribonucleoside - Pyrimidine nucleoside - 6-oxopurine - Hypoxanthine - Trialkylglycerol - Imidazopyrimidine - Purine - Pyrimidone - Glycerolipid - Glycerol ether - Hydropyrimidine - N-substituted imidazole - Pyrimidine - Azole - Imidazole - Heteroaromatic compound - Oxolane - Vinylogous amide - Azo imide - Urea - Azo compound - Lactam - Azacycle - Oxacycle - Organoheterocyclic compound - Dialkyl ether - Ether - Organooxygen compound - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Organonitrogen compound - Organic nitrogen compound - Organic salt - Organic zwitterion - 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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