Structure Information
Structure

Compound Identification

SMILES

NC1=NC(=O)C2=C(N1)N(C=N2)C1CCC(COP([O-])(=O)OP([O-])(=O)OP([O-])(=O)OC2=CC3=C(C=C2)C(=CC(=O)O3)C(F)(F)F)O1

InChIKey

InChIKey=KCVXTRBUIBOLMH-UHFFFAOYSA-K

Formula

C20H16F3N5O14P3

Mass

700.287

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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 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-oxopurine - Benzopyran - Hypoxanthine - 1-benzopyran - Imidazopyrimidine - Purine - Aminopyrimidine - Pyranone - Pyrimidone - Alkyl phosphate - Pyrimidine - Pyran - Benzenoid - Phosphoric acid ester - Organic phosphoric acid derivative - N-substituted imidazole - Azole - Heteroaromatic compound - Imidazole - Oxolane - Vinylogous amide - Lactone - Oxacycle - Organoheterocyclic compound - Azacycle - Primary amine - Organic oxygen compound - Organohalogen compound - Organofluoride - Organonitrogen compound - Alkyl halide - Alkyl fluoride - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Organooxygen compound - Amine - Organic anion - 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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