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Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](N=[N+]=[N-])[C@H]1O

InChIKey

InChIKey=DANBERCPRJIPTD-QYYRPYCUSA-N

Formula

C10H15N8O12P3

Mass

532.195

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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-5-phosphate - Pentose phosphate - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Monosaccharide phosphate - Pentose monosaccharide - Imidazopyrimidine - Purine - Aminopyrimidine - Monoalkyl phosphate - Alkyl phosphate - Organic phosphoric acid derivative - Pyrimidine - Imidolactam - N-substituted imidazole - Monosaccharide - Phosphoric acid ester - Azole - Imidazole - Heteroaromatic compound - Oxolane - Secondary alcohol - Azo compound - Azo imide - Organoheterocyclic compound - Azacycle - Oxacycle - Primary amine - Amine - Alcohol - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Organic salt - Organonitrogen compound - Organic oxygen compound - Organic zwitterion - Organooxygen 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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