Structure Information
Structure

Compound Identification

SMILES

CC[C@H](C)[C@H](N)C(=O)OCC(CO)OC(=O)CCC(=O)OC[C@@H]1CC[C@@H](O1)N1C=NC2=C1NC=NC2=O

InChIKey

InChIKey=RZKOHBVVSYVPIR-JFAPPWHYSA-N

Formula

C23H33N5O9

Mass

523.543

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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 - Isoleucine or derivatives - Alpha-amino acid ester - 1,2-acyl-sn-glycerol - 6-oxopurine - Alpha-amino acid or derivatives - Diacylglycerol - Hypoxanthine - Diradylglycerol - Purine - Tricarboxylic acid or derivatives - Imidazopyrimidine - Glycerolipid - Fatty acid ester - Pyrimidone - Fatty acyl - N-substituted imidazole - Pyrimidine - Azole - Heteroaromatic compound - Imidazole - Vinylogous amide - Oxolane - Amino acid or derivatives - Carboxylic acid ester - Carboxylic acid derivative - Organoheterocyclic compound - Azacycle - Oxacycle - Primary amine - Organic oxygen compound - Alcohol - Primary aliphatic amine - Carbonyl group - Organic nitrogen compound - Organic oxide - Amine - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Primary alcohol - 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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