Structure Information
Structure

Compound Identification

SMILES

CC1=CN([C@H]2C[C@H](N)[C@@H](CO[C@@H]3O[C@@H]([C@@H](O)[C@H](O)[C@H]3O)C(O)=O)O2)C(=O)NC1=O

InChIKey

InChIKey=XOYCLJDJUKHHHS-LHBOOPKSSA-N

Formula

C16H23N3O10

Mass

417.371

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Pyrimidine nucleosides

Subclass

Pyrimidine 2',3'-dideoxyribonucleosides

Intermediate Tree Nodes

Not available

Direct Parent

Pyrimidine 2',3'-dideoxyribonucleosides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Pyrimidine 2',3'-dideoxyribonucleoside - O-glucuronide - 1-o-glucuronide - Glucuronic acid or derivatives - O-glycosyl compound - Glycosyl compound - Pyrimidone - Beta-hydroxy acid - Pyrimidine - Pyran - Oxane - Monosaccharide - Hydroxy acid - Hydropyrimidine - Heteroaromatic compound - Vinylogous amide - Tetrahydrofuran - Amino acid - Urea - Secondary alcohol - Lactam - Amino acid or derivatives - Oxacycle - Azacycle - Organoheterocyclic compound - Polyol - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Acetal - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Carbonyl group - Amine - Alcohol - Aromatic heteromonocyclic compound

Description

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

External Descriptors

Not available

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