Structure Information
Structure

Compound Identification

SMILES

CNC1=NC2=C(C=C(Cl)C=C2)C(=NC1)C1=CC=CN1.CC1=CN([C@H]2C[C@H](N=[N+]=[N-])[C@@H](CO)O2)C(=O)NC1=O

InChIKey

InChIKey=PBBDFKDFNVPUQJ-XKPASDJRSA-N

Formula

C24H26ClN9O4

Mass

539.98

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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

Not available

Substituents

Pyrimidine 2',3'-dideoxyribonucleoside - Benzodiazepine - 1,4-benzodiazepine - Pyrimidone - Aryl chloride - Aryl halide - Hydropyrimidine - Pyrimidine - Substituted pyrrole - Benzenoid - Imidolactam - Heteroaromatic compound - Pyrrole - Vinylogous amide - Oxolane - Urea - Azo compound - Azo imide - Ketimine - Lactam - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Amidine - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid amidine - Organic salt - Organohalogen compound - Organochloride - Organonitrogen compound - Imine - Amine - Organooxygen compound - Organic nitrogen compound - Primary alcohol - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Alcohol - Organic zwitterion - Aromatic heteropolycyclic 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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