Structure Information
Structure

Compound Identification

SMILES

CN[C@@H]1[C@@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)O[C@H]([C@@H]1O)N1C=NC2=C1N=CN=C2N

InChIKey

InChIKey=AOXISSGNFZFAKD-HUKYDQBMSA-N

Formula

C11H19N6O12P3

Mass

520.224

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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 3'-deoxyribonucleoside triphosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine 3'-deoxyribonucleoside triphosphate - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - Monosaccharide phosphate - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Monoalkyl phosphate - Organic phosphoric acid derivative - N-substituted imidazole - Monosaccharide - Phosphoric acid ester - Alkyl phosphate - Pyrimidine - Imidolactam - Oxolane - Heteroaromatic compound - Imidazole - Azole - 1,2-aminoalcohol - Secondary alcohol - Oxacycle - Secondary amine - Secondary aliphatic amine - Organoheterocyclic compound - Azacycle - Organic nitrogen compound - Organic oxygen compound - Primary amine - Organic oxide - Hydrocarbon derivative - Amine - Alcohol - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine 3'-deoxyribonucleoside triphosphates. These are purine nucleotides with triphosphate group linked to the ribose moiety lacking a hydroxyl group at position 3.

External Descriptors

Not available

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