Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1N=CN2C1CCC(COP(O)(=O)OC2=CNC3=C2C=C(I)C=C3)O1

InChIKey

InChIKey=XFHKYFAJAREYQH-UHFFFAOYSA-N

Formula

C18H18IN6O5P

Mass

556.257

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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 monophosphates

Direct Parent

Purine 2',3'-dideoxyribonucleoside monophosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine 2',3'-dideoxyribonucleoside monophosphate - Purine 2',3'-dideoxyribonucleoside - Purine nucleoside - 6-aminopurine - Imidazopyrimidine - Indole - Indole or derivatives - Purine - Aminopyrimidine - Monoalkyl phosphate - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Aryl iodide - Aryl halide - Pyrimidine - Substituted pyrrole - Alkyl phosphate - Benzenoid - Imidolactam - Heteroaromatic compound - Pyrrole - Imidazole - Tetrahydrofuran - Azole - Organoheterocyclic compound - Azacycle - Oxacycle - Hydrocarbon derivative - Organohalogen compound - Organoiodide - Amine - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Primary amine - Organic oxygen compound - Organopnictogen compound - Organic oxide - Aromatic heteropolycyclic compound

Description

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

External Descriptors

Not available

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