Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCCCCCCCCCCC(=O)NC([C@@H](C)OCC)C1=NC2=C(N=CN2[C@@H]2O[C@H](COP(O)(=O)OP(O)(O)=O)C[C@H]2F)C(N)=N1

InChIKey

InChIKey=VGDNSAWPEJAACM-MTWXVTQQSA-N

Formula

C33H59FN6O10P2

Mass

780.813

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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 - Monoalkyl phosphate - Organic phosphoric acid derivative - N-substituted imidazole - N-acyl-amine - Phosphoric acid ester - Fatty amide - Fatty acyl - Pyrimidine - Imidolactam - Alkyl phosphate - Oxolane - Azole - Heteroaromatic compound - Imidazole - Amino acid or derivatives - Secondary carboxylic acid amide - Carboxamide group - Oxacycle - Carboxylic acid derivative - Dialkyl ether - Ether - Azacycle - Organoheterocyclic compound - Organic oxygen compound - Amine - Alkyl halide - Alkyl fluoride - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Primary amine - Organooxygen compound - Organonitrogen compound - Organohalogen compound - Organofluoride - 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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