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=NC4=C3NC(N)=NC4=O)=C2)N=C2C=C(Cl)C(=O)C(Cl)=C12

InChIKey

InChIKey=HSYKVGIJHUZFEY-UHFFFAOYSA-J

Formula

C25H22Cl2N6O17P4

Mass

873.27

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleotides

Subclass

Purine deoxyribonucleotides

Intermediate Tree Nodes

Purine deoxyribonucleoside polyphosphates

Direct Parent

Purine 2'-deoxyribonucleoside polyphosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine 2'-deoxyribonucleoside polyphosphate - Acridine - Benzoquinoline - 6-oxopurine - Hypoxanthine - Purine - Imidazopyrimidine - Aminopyrimidine - Pyrimidone - Phosphoric acid ester - Pyrimidine - Organic phosphoric acid derivative - N-substituted imidazole - Benzenoid - Alkyl phosphate - Alpha-haloketone - Oxolane - Alpha-chloroketone - Azole - Vinylogous amide - Imidazole - Heteroaromatic compound - Ketimine - Secondary alcohol - Ketone - Cyclic ketone - Oxacycle - Azacycle - Chloroalkene - Haloalkene - Organoheterocyclic compound - Vinyl halide - Vinyl chloride - Organic oxide - Imine - Amine - Alcohol - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - Organohalogen compound - Hydrocarbon derivative - Organochloride - Organonitrogen compound - Organooxygen compound - Primary amine - Organic anion - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine 2'-deoxyribonucleoside polyphosphates. These are purine nucleotides with 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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