Structure Information
Structure

Compound Identification

SMILES

CC(COC(=O)O[C@H]1C[C@@H](O[C@@H]1COP(=O)(OCCC#N)O[C@H]1C[C@@H](O[C@@H]1CO)N1C=C(C)C(=O)NC1=O)N1C=C(C)C(=O)NC1=O)C1=CC=CC=C1[N+]([O-])=O

InChIKey

InChIKey=KOZDRTFLPUSBCW-YGFSZFHJSA-N

Formula

C33H39N6O16P

Mass

806.675

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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 - Ribonucleoside 3'-phosphate - Nitrobenzene - Nitroaromatic compound - Trialkyl phosphate - Pyrimidone - Monocyclic benzene moiety - Carbonic acid diester - Hydropyrimidine - Organic phosphoric acid derivative - Benzenoid - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Vinylogous amide - Oxolane - Heteroaromatic compound - Lactam - C-nitro compound - Carbonic acid derivative - Organic nitro compound - Urea - Allyl-type 1,3-dipolar organic compound - Organoheterocyclic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Azacycle - Oxacycle - Carbonitrile - Nitrile - Organic oxoazanium - Organic salt - Hydrocarbon derivative - Organic nitrogen compound - Organic oxide - Organonitrogen compound - Organooxygen compound - Alcohol - Cyanide - Carbonyl group - Primary alcohol - Organic oxygen compound - Organic zwitterion - 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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