Structure Information
Structure

Compound Identification

SMILES

[I-].C[N+]1=CC=CC=C1C(OP(O)(=O)OC[C@H]1O[C@H](C[C@@H]1O)N1C=NC2=C1NC(N)=NC2=O)OP(O)(=O)OC[C@H]1O[C@H](C[C@@H]1O)N1C=NC2=C1NC(N)=NC2=O

InChIKey

InChIKey=FKZKBHIDTSWVFD-TVRDLCMASA-N

Formula

C27H34IN11O14P2

Mass

925.484

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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 - Aminopyrimidine - N-methylpyridinium - Pyrimidone - Dialkyl phosphate - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Pyridine - Pyridinium - Pyrimidine - Alkyl phosphate - Azole - Vinylogous amide - Heteroaromatic compound - Imidazole - Oxolane - Secondary alcohol - Azacycle - Organoheterocyclic compound - Oxacycle - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Amine - Primary amine - Organic oxide - Organic iodide salt - Organic zwitterion - Organic salt - 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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