Structure Information
Structure

Compound Identification

SMILES

CC1(C)C2=C(C=CC(OP([O-])(=O)OP([O-])(=O)OP([O-])(=O)OP([O-])(=O)OCC3CCC(O3)N3C=NC4=C3NC(N)=NC4=O)=C2)N=C2C=C(Cl)C(=O)C(Cl)=C12

InChIKey

InChIKey=ZKJYWOIOZLNKOY-UHFFFAOYSA-J

Formula

C25H22Cl2N6O16P4

Mass

857.27

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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',3'-dideoxyribonucleoside polyphosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine 2',3'-dideoxyribonucleoside polyphosphate - Purine 2',3'-dideoxyribonucleoside - Purine nucleoside - Acridine - Benzoquinoline - 6-oxopurine - Hypoxanthine - Purine - Imidazopyrimidine - Aminopyrimidine - Pyrimidone - Pyrimidine - Phosphoric acid ester - Alkyl phosphate - Organic phosphoric acid derivative - Benzenoid - N-substituted imidazole - Alpha-chloroketone - Azole - Oxolane - Alpha-haloketone - Heteroaromatic compound - Vinylogous amide - Imidazole - Ketimine - Ketone - Cyclic ketone - Vinyl chloride - Vinyl halide - Oxacycle - Azacycle - Chloroalkene - Haloalkene - Organoheterocyclic compound - Amine - Primary amine - Organic oxygen compound - Organic nitrogen compound - Imine - Organohalogen compound - Organochloride - Carbonyl group - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organic anion - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine 2',3'-dideoxyribonucleoside polyphosphates. These are purine nucleotides with polyphosphate (with 4 or more phosphate) group linked to the ribose moiety lacking a hydroxyl group at positions 2 and 3.

External Descriptors

Not available

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