Structure Information
Structure

Compound Identification

SMILES

COC1=CC=C(C=C1)C(OC[C@H]1O[C@H](C[C@@H]1OP(O)(=O)OC[C@H]1O[C@H](C[C@@H]1O)N1C=C(C)C(=O)NC1=O)N1C=C(C)C(=O)NC1=O)(C1=CC=CC=C1)C1=CC=C(OC)C=C1

InChIKey

InChIKey=NRHRFDFHTTWCBH-UWNKZCSISA-N

Formula

C41H45N4O14P

Mass

848.799

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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 - Triphenyl compound - Ribonucleoside 3'-phosphate - Benzylether - Phenoxy compound - Anisole - Phenol ether - Methoxybenzene - Alkyl aryl ether - Pyrimidone - Dialkyl phosphate - Monocyclic benzene moiety - Pyrimidine - Phosphoric acid ester - Benzenoid - Organic phosphoric acid derivative - Alkyl phosphate - Hydropyrimidine - Heteroaromatic compound - Vinylogous amide - Oxolane - Lactam - Urea - Secondary alcohol - Azacycle - Oxacycle - Ether - Dialkyl ether - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Organic oxygen compound - 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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