Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCCCCOC(CCCCCCCCC)C(C)OOP(O)(=O)OP(=O)(OCCC)OC[C@@H]1CC[C@@H](O1)N1C=NC2=C1N=C(F)N=C2N

InChIKey

InChIKey=OEKZLQFLVBONAV-DWWKXAEXSA-N

Formula

C36H66FN5O10P2

Mass

809.895

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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 diphosphates

Direct Parent

Purine 2',3'-dideoxyribonucleoside diphosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine 2',3'-dideoxyribonucleoside diphosphate - Purine 2',3'-dideoxyribonucleoside - Purine nucleoside - 6-aminopurine - Organic pyrophosphate - Imidazopyrimidine - Purine - Aminopyrimidine - Halopyrimidine - 2-halopyrimidine - Dialkyl phosphate - Alkyl phosphate - Pyrimidine - Imidolactam - Aryl fluoride - Aryl halide - Phosphoric acid ester - N-substituted imidazole - Organic phosphoric acid derivative - Heteroaromatic compound - Azole - Oxolane - Imidazole - Azacycle - Organoheterocyclic compound - Oxacycle - Dialkyl ether - Ether - Organooxygen compound - Amine - Hydrocarbon derivative - Primary amine - Organic oxide - Organic oxygen compound - Organonitrogen compound - Organohalogen compound - Organofluoride - Organic nitrogen compound - Aromatic heteropolycyclic compound

Description

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

External Descriptors

Not available

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