Structure Information
Structure

Compound Identification

SMILES

CC1=CN(C2CC(O)C(COP(O)(=O)OP(O)(=O)OP(O)(=O)OP(O)(=O)OC3=CC4=C(C=C3)N=C3C=C(Cl)C(=O)C(Cl)=C3C4(C)C)O2)C(=O)NC1=O

InChIKey

InChIKey=DRJPNZJEPUGJAP-UHFFFAOYSA-N

Formula

C25H27Cl2N3O18P4

Mass

852.29

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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 - Pyrimidone - Monoalkyl phosphate - Hydropyrimidine - Alkyl phosphate - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Benzenoid - Alpha-haloketone - Alpha-chloroketone - Heteroaromatic compound - Oxolane - Vinylogous amide - Cyclic ketone - Lactam - Ketone - Ketimine - Secondary alcohol - Urea - Oxacycle - Azacycle - Chloroalkene - Haloalkene - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Vinyl halide - Vinyl chloride - Organohalogen compound - Alcohol - Organochloride - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Carbonyl group - Organic oxide - Imine - Hydrocarbon derivative - Organic nitrogen compound - 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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