Structure Information
Structure

Compound Identification

SMILES

[NH4+].[NH4+].CCCCC1=CC=C(NC2=NC(=O)C3=C(N2)N(C=N3)[C@H]2CC(O)[C@@H](COP(O)(O)=O)O2)C=C1

InChIKey

InChIKey=VDXSKWXDPXGTKR-FXIYJNFOSA-P

Formula

C20H34N7O7P

Mass

515.507

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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 - 6-oxopurine - Hypoxanthine - Imidazopyrimidine - Purine - Aniline or substituted anilines - Aminopyrimidine - Pyrimidone - Monoalkyl phosphate - Monocyclic benzene moiety - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Benzenoid - Vinylogous amide - Heteroaromatic compound - Oxolane - Azole - Quaternary ammonium salt - Imidazole - Secondary alcohol - Azacycle - Oxacycle - Organoheterocyclic compound - Organic nitrogen compound - Organic oxygen compound - Hydrocarbon derivative - Alcohol - Organic oxide - Amine - Organonitrogen compound - Organooxygen compound - Organic cation - 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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