Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1O[C@H](C[C@@H]1N1C=NC(=C1)[N+]([O-])=O)N1C=C(Cl)C(=O)NC1=O

InChIKey

InChIKey=MOPJAMVVBHXJQG-QXFUBDJGSA-N

Formula

C12H12ClN5O6

Mass

357.71

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