Structure Information
Structure

Compound Identification

SMILES

CC1=CN([C@H]2C[C@H](F)[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=DVUGHAFFGKWXDR-LHBOOPKSSA-N

Formula

C16H21FN2O10

Mass

420.346

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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 - Glycosyl compound - O-glycosyl compound - Beta-hydroxy acid - Pyrimidone - Hydroxy acid - Hydropyrimidine - Oxane - Pyran - Pyrimidine - Monosaccharide - Vinylogous amide - Oxolane - Heteroaromatic compound - Lactam - Urea - Secondary alcohol - Polyol - Carboxylic acid derivative - Carboxylic acid - Acetal - Organoheterocyclic compound - Azacycle - Oxacycle - Monocarboxylic acid or derivatives - Organonitrogen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organohalogen compound - Organofluoride - Carbonyl group - Organic nitrogen compound - Alkyl halide - Organooxygen compound - Alkyl fluoride - 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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