Structure Information
Structure

Compound Identification

SMILES

CC1=NC(=CN1[C@H]1C[C@@H](O[C@@H]1CO)N1C=C(Cl)C(=O)NC1=O)[N+]([O-])=O

InChIKey

InChIKey=SVZJGTXQXLFMNW-IQJOONFLSA-N

Formula

C13H14ClN5O6

Mass

371.73

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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 - 1,2,4-trisubstituted-imidazole - Nitroaromatic compound - Nitroimidazole - Trisubstituted imidazole - Halopyrimidine - Pyrimidone - Aryl chloride - Aryl halide - Hydropyrimidine - N-substituted imidazole - Pyrimidine - Imidolactam - Heteroaromatic compound - Tetrahydrofuran - Vinylogous amide - Azole - Imidazole - Urea - Organic nitro compound - Lactam - C-nitro compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Oxacycle - Azacycle - Organoheterocyclic compound - Organic oxoazanium - Organic zwitterion - Organopnictogen compound - Organohalogen compound - Organic nitrogen compound - Organochloride - Organonitrogen compound - Organic oxygen compound - Organooxygen compound - Primary alcohol - Organic oxide - Alcohol - Hydrocarbon derivative - 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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