Structure Information
Structure

Compound Identification

SMILES

CC1(C)C2=C(C=CC(OP([O-])(=O)OP([O-])(=O)OP([O-])(=O)OP([O-])(=O)OCC3OC(CC3O)N3C=CC(N)=NC3=O)=C2)N=C2C=C(Cl)C(=O)C(Cl)=C12

InChIKey

InChIKey=HZFQYNPTNITPGN-UHFFFAOYSA-J

Formula

C24H22Cl2N4O17P4

Mass

833.25

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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 polyphosphates

Direct Parent

Pyrimidine 2'-deoxyribonucleoside polyphosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Pyrimidine 2'-deoxyribonucleoside polyphosphate - Acridine - Benzoquinoline - Aminopyrimidine - Pyrimidone - Hydropyrimidine - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Imidolactam - Benzenoid - Alkyl phosphate - Alpha-haloketone - Alpha-chloroketone - Heteroaromatic compound - Oxolane - Ketimine - Ketone - Secondary alcohol - Cyclic ketone - Vinyl halide - Organoheterocyclic compound - Haloalkene - Vinyl chloride - Chloroalkene - Azacycle - Oxacycle - Organic oxygen compound - Primary amine - Organonitrogen compound - Organochloride - Organooxygen compound - Organohalogen compound - Alcohol - Organic nitrogen compound - Imine - Hydrocarbon derivative - Carbonyl group - Organic oxide - Amine - Organic anion - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as pyrimidine 2'-deoxyribonucleoside polyphosphates. These are pyrimidine nucleotides with a polyphosphate (with 4 or more phosphate) group linked to the ribose moiety lacking a hydroxyl group at position 2.

External Descriptors

Not available

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