Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1N=CN2[C@H]1CC[C@@H](COP(O)(=O)OP(O)(=O)OP(O)(=O)OC2=CC3=C(C=C2)C=C(C#N)C(=O)O3)O1

InChIKey

InChIKey=SUQKCFBUHGCGQX-GOEBONIOSA-N

Formula

C20H19N6O13P3

Mass

644.322

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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 triphosphates

Direct Parent

Purine 2',3'-dideoxyribonucleoside triphosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine 2',3'-dideoxyribonucleoside triphosphate - Purine 2',3'-dideoxyribonucleoside - Purine nucleoside - Coumarin - 6-aminopurine - Benzopyran - 1-benzopyran - Imidazopyrimidine - Purine - Aminopyrimidine - Pyranone - Monoalkyl phosphate - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Imidolactam - Pyran - Pyrimidine - Benzenoid - Alkyl phosphate - Heteroaromatic compound - Imidazole - Azole - Oxolane - Lactone - Organoheterocyclic compound - Azacycle - Oxacycle - Nitrile - Carbonitrile - Primary amine - Organic nitrogen compound - Hydrocarbon derivative - Amine - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Cyanide - Organic oxide - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine 2',3'-dideoxyribonucleoside triphosphates. These are purine nucleotides with triphosphate group linked to the ribose moiety lacking a hydroxyl group at positions 2 and 3.

External Descriptors

Not available

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