Structure Information
Structure

Compound Identification

SMILES

CC1=CN([C@H]2C[C@H](SCCNC(=O)OCC3C4=CC=CC=C4C4=CC=CC=C34)[C@@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)O2)C(=O)NC1=O

InChIKey

InChIKey=QJTPVZKBBZRHDC-TZRRMPRUSA-N

Formula

C27H32N3O15P3S

Mass

763.54

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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 triphosphates

Direct Parent

Pyrimidine 2',3'-dideoxyribonucleoside triphosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Pyrimidine 2',3'-dideoxyribonucleoside triphosphate - 2',3'-dideoxy-3'-thionucleoside triphosphate - 2',3'-dideoxy-3'-thionucleoside - Fluorene - Pyrimidone - Monoalkyl phosphate - Hydropyrimidine - Alkyl phosphate - Benzenoid - Pyrimidine - Organic phosphoric acid derivative - Phosphoric acid ester - Carbamic acid ester - Vinylogous amide - Oxolane - Heteroaromatic compound - Lactam - Urea - Oxacycle - Azacycle - Organoheterocyclic compound - Dialkylthioether - Sulfenyl compound - Thioether - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Carbonyl group - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as pyrimidine 2',3'-dideoxyribonucleoside triphosphates. These are pyrimidine nucleotides with triphosphate group linked to the ribose moiety lacking a hydroxyl group at positions 2 and 3.

External Descriptors

Not available

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