Structure Information
Structure

Compound Identification

SMILES

CC(=O)CCC(=O)O[C@H]1C[C@@H](O[C@@H]1CO[P+]([O-])(OC[C@H]1O[C@H](C[C@@H]1OC(=O)CCC(C)=O)N1C=C(C)C(OC2=CC=CC=C2)=NC1=O)SCCC#N)N1C=C(C)C(OC2=CC=CC=C2)=NC1=O

InChIKey

InChIKey=QPSTWRRWMSYVSI-MKQWCXJJSA-N

Formula

C45H50N5O15PS

Mass

963.95

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Pyrimidine nucleosides

Subclass

Pyrimidine 2'-deoxyribonucleosides

Intermediate Tree Nodes

Not available

Direct Parent

Pyrimidine 2'-deoxyribonucleosides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Pyrimidine 2'-deoxyribonucleoside - Diaryl ether - Phenoxy compound - Gamma-keto acid - Phenol ether - Fatty acid ester - Pyrimidone - Monocyclic benzene moiety - Dicarboxylic acid or derivatives - Hydropyrimidine - Keto acid - Fatty acyl - Pyrimidine - Benzenoid - Heteroaromatic compound - Oxolane - Carboxylic acid ester - Ketone - Sulfenyl compound - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Organothiophosphorus compound - Ether - Oxacycle - Nitrile - Carbonitrile - Organic salt - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Cyanide - Organic oxygen compound - Organosulfur compound - Organic nitrogen compound - Carbonyl group - Organic zwitterion - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as pyrimidine 2'-deoxyribonucleosides. These are compounds consisting of a pyrimidine linked to a ribose which lacks a hydroxyl group at position 2.

External Descriptors

Not available

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