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Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCCCCCCCCCCCOC(COP(O)(=O)OCC1CCC(O1)N1C=NC2=C1NC=NC2=O)COP(O)(=O)OCC1OC(CC1N=[N+]=[N-])N1C=C(C)C(=O)NC1=O

InChIKey

InChIKey=VIMPOHVWZIUTHF-UHFFFAOYSA-N

Formula

C41H67N9O14P2

Mass

971.984

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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 - Imidazopyrimidine - Purine - Dialkyl phosphate - Glycerol ether - Pyrimidone - Hydropyrimidine - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Alkyl phosphate - Pyrimidine - Azole - Imidazole - Heteroaromatic compound - Oxolane - Vinylogous amide - Urea - Azo imide - Lactam - Azo compound - Azacycle - Organoheterocyclic compound - Dialkyl ether - Ether - Oxacycle - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Organic salt - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic zwitterion - 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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