Structure Information
Structure

Compound Identification

SMILES

CC(C)(C)C(=O)SCCOP(O)(=O)OCC1CCC(O1)N1C=NC2=C1N=CN=C2N

InChIKey

InChIKey=HEXGHMQDKRAXQR-UHFFFAOYSA-N

Formula

C17H26N5O6PS

Mass

459.46

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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 - Purine - Aminopyrimidine - Dialkyl phosphate - N-substituted imidazole - Imidolactam - Organic phosphoric acid derivative - Alkyl phosphate - Phosphoric acid ester - Pyrimidine - Heteroaromatic compound - Azole - Imidazole - Oxolane - Thiocarboxylic acid ester - Amino acid or derivatives - Carbothioic s-ester - Thiocarboxylic acid or derivatives - Oxacycle - Carboxylic acid derivative - Organoheterocyclic compound - Azacycle - Sulfenyl compound - Hydrocarbon derivative - Organic nitrogen compound - Organic oxygen compound - Amine - Carbonyl group - Primary amine - Organonitrogen compound - Organooxygen compound - Organosulfur 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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