Structure Information
Structure

Compound Identification

SMILES

C[N+]1=CC=CC(OCCCCCCCOC2=C[N+](C)=C(C=C2)C(OP(O)(=O)OC[C@H]2O[C@H](C[C@@H]2O)N2C=NC3=C2N=CN=C3N)OP(O)(=O)OC[C@H]2O[C@H](C[C@@H]2O)N2C=NC3=C2N=CN=C3N)=C1C=O

InChIKey

InChIKey=PERPXLFFTZWVBJ-HKROBGSISA-P

Formula

C41H54N12O15P2

Mass

1016.898

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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-aminopurine - Purine - Imidazopyrimidine - 2-pyridine carboxaldehyde - Alkyl aryl ether - Dialkyl phosphate - Aryl-aldehyde - Aminopyrimidine - N-methylpyridinium - Pyridinium - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Imidolactam - Pyridine - Alkyl phosphate - Pyrimidine - Azole - Imidazole - Heteroaromatic compound - Oxolane - Secondary alcohol - Azacycle - Organoheterocyclic compound - Ether - Oxacycle - Aldehyde - Hydrocarbon derivative - Alcohol - Organic nitrogen compound - Organic oxide - Amine - Primary amine - Organonitrogen compound - Organooxygen compound - Organic oxygen 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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