Structure Information
Structure

Compound Identification

SMILES

CC1=CC(=O)OC2=C1C=C(OP([O-])(=O)OP([O-])(=O)OP([O-])(=O)OP([O-])(=O)OC[C@H]1OC(CC1O)N1C=NC3=C1N=CN=C3N)C=C2

InChIKey

InChIKey=HWRVWHRCDIICAX-OGVSOVDVSA-J

Formula

C20H19N5O17P4

Mass

725.287

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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 - Coumarin - 6-aminopurine - Benzopyran - 1-benzopyran - Imidazopyrimidine - Purine - Aminopyrimidine - Pyranone - Imidolactam - Benzenoid - N-substituted imidazole - Alkyl phosphate - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Pyran - Azole - Imidazole - Heteroaromatic compound - Oxolane - Lactone - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Organooxygen compound - Organonitrogen compound - Amine - Organic nitrogen compound - Organic oxide - Organic oxygen compound - Primary amine - Hydrocarbon derivative - Alcohol - 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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