Structure Information
Structure

Compound Identification

SMILES

CCOC1=NC(N)=NC2=C1N=CN2C1CC(O)C(COP([O-])([O-])=O)O1

InChIKey

InChIKey=WXGDGPAAUVLZNL-UHFFFAOYSA-L

Formula

C12H16N5O7P

Mass

373.263

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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'-deoxyribonucleoside monophosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine 2'-deoxyribonucleoside monophosphate - Hypoxanthine - Imidazopyrimidine - Purine - Alkyl aryl ether - Aminopyrimidine - N-substituted imidazole - Organic phosphoric acid derivative - Alkyl phosphate - Pyrimidine - Phosphoric acid ester - Azole - Imidazole - Heteroaromatic compound - Oxolane - Secondary alcohol - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Organic oxygen compound - Amine - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Alcohol - Organopnictogen compound - Organonitrogen compound - Organooxygen compound - Primary amine - Organic anion - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine 2'-deoxyribonucleoside monophosphates. These are purine nucleotides with monophosphate group linked to the ribose moiety lacking a hydroxyl group at position 2.

External Descriptors

Not available

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