Structure Information
Structure

Compound Identification

SMILES

CC(=O)O[C@H]1C[C@@H](O[C@@H]1COP(=O)(OC[C@H]1O[C@H](C[C@@H]1OC(C)=O)N1C=C(C)C(=O)NC1=O)OC1=CC=C(C=C1)S(C)(=O)=O)N1C=C(C)C(=O)NC1=O

InChIKey

InChIKey=MAONPDWWYFLBAZ-UIQLYKSZSA-N

Formula

C31H37N4O16PS

Mass

784.68

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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 - Benzenesulfonyl group - Phenoxy compound - Pyrimidone - Dialkyl phosphate - Monocyclic benzene moiety - Dicarboxylic acid or derivatives - Hydropyrimidine - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Benzenoid - Heteroaromatic compound - Sulfone - Sulfonyl - Tetrahydrofuran - Vinylogous amide - Carboxylic acid ester - Urea - Lactam - Azacycle - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Organic nitrogen compound - Organonitrogen compound - Organic oxide - Organooxygen compound - Organopnictogen compound - Organic oxygen compound - Carbonyl group - Organosulfur compound - Hydrocarbon derivative - 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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