Structure Information
Structure

Compound Identification

SMILES

CCCCC1=CC=C(NC2=NC3=C(N=CN3[C@@H]3O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@@H]3N=[N+]=[N-])C(N)=N2)C=C1

InChIKey

InChIKey=IWKLVLPXGABJRS-QHHYFVSCSA-N

Formula

C20H28N9O12P3

Mass

679.416

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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 triphosphates

Direct Parent

Purine 2'-deoxyribonucleoside triphosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine 2'-deoxyribonucleoside triphosphate - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Imidazopyrimidine - Purine - Aniline or substituted anilines - Aminopyrimidine - Monoalkyl phosphate - Monocyclic benzene moiety - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Benzenoid - Imidolactam - Azole - Heteroaromatic compound - Imidazole - Oxolane - Azo imide - Azo compound - Secondary alcohol - Oxacycle - Azacycle - Secondary amine - Organoheterocyclic compound - Organonitrogen compound - Amine - Organic oxide - Organic nitrogen compound - Alcohol - Organic oxygen compound - Organic salt - Organic zwitterion - Organooxygen compound - Primary amine - Hydrocarbon derivative - Aromatic heteropolycyclic compound

Description

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

External Descriptors

Not available

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