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-N

Formula

C24H26Cl2N4O17P4

Mass

837.28

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