Structure Information
Structure

Compound Identification

SMILES

NC1=NC(=O)N(C=C1)[C@H]1CC[C@@H](CO)O1.OC[C@@H]1CC[C@@H](O1)N1C=NC2=C1NC=NC2=O.CC1=CN([C@H]2C[C@H](N=[N+]=[N-])[C@@H](CO)O2)C(=O)NC1=O

InChIKey

InChIKey=OWMCHPAOTUQULO-GXIWTGGYSA-N

Formula

C29H38N12O10

Mass

714.697

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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

Not available

Substituents

Purine 2',3'-dideoxyribonucleoside - Pyrimidine 2',3'-dideoxyribonucleoside - Pyrimidine nucleoside - 6-oxopurine - Hypoxanthine - Purinone - Imidazopyrimidine - Purine - Aminopyrimidine - Pyrimidone - Hydropyrimidine - N-substituted imidazole - Pyrimidine - Imidolactam - Azole - Imidazole - Heteroaromatic compound - Oxolane - Vinylogous amide - Urea - Azo compound - Azo imide - Lactam - Azacycle - Organoheterocyclic compound - Oxacycle - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organic oxide - Alcohol - Hydrocarbon derivative - Organic salt - Organic zwitterion - Amine - Primary alcohol - Primary amine - Organic nitrogen 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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