Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCCCCCCCCC(=O)OCC(COP(O)(=O)OC[C@@H]1CC[C@@H](O1)N1C=NC2=C1NC=NC2=O)OC(=O)CCCCCCCCCCCCCCC

InChIKey

InChIKey=MJKQNINGUQHQRN-JVOCVZPZSA-N

Formula

C45H79N4O10P

Mass

867.119

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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-oxopurine - Hypoxanthine - Glycerophospholipid - Imidazopyrimidine - Purine - Fatty acid ester - Pyrimidone - Dialkyl phosphate - N-substituted imidazole - Alkyl phosphate - Dicarboxylic acid or derivatives - Pyrimidine - Organic phosphoric acid derivative - Fatty acyl - Phosphoric acid ester - Azole - Imidazole - Heteroaromatic compound - Oxolane - Vinylogous amide - Carboxylic acid ester - Azacycle - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Carbonyl group - 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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