Structure Information
Structure

Compound Identification

SMILES

O[C@H]1C[C@@H](O[C@@H]1COP(O)(O)=O)N1C=C(\C=C\C2=CC(=CC=C2)[N+]([O-])=O)C(=O)NC1=O

InChIKey

InChIKey=IOCFJZURCLIIAL-NMJJRHIFSA-N

Formula

C17H18N3O10P

Mass

455.316

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Pyrimidine nucleotides

Subclass

Pyrimidine deoxyribonucleotides

Intermediate Tree Nodes

Pyrimidine deoxyribonucleoside monophosphates

Direct Parent

Pyrimidine 2'-deoxyribonucleoside monophosphates

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Pyrimidine 2'-deoxyribonucleoside monophosphate - Nitrobenzene - Nitroaromatic compound - Styrene - Monoalkyl phosphate - Pyrimidone - Alkyl phosphate - Monocyclic benzene moiety - Hydropyrimidine - Benzenoid - Pyrimidine - Phosphoric acid ester - Organic phosphoric acid derivative - Vinylogous amide - Oxolane - Heteroaromatic compound - Urea - C-nitro compound - Secondary alcohol - Organic nitro compound - Lactam - Organic oxoazanium - Oxacycle - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organooxygen compound - Organonitrogen compound - Alcohol - Organic nitrogen compound - Organic oxygen compound - Organic salt - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic cation - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as pyrimidine 2'-deoxyribonucleoside monophosphates. These are pyrimidine nucleotides with a monophosphate group linked to the ribose moiety lacking a hydroxyl group at position 2.

External Descriptors

Not available

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