Structure Information
Structure

Compound Identification

SMILES

OC1C(COP(O)(=O)OP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=CC(=O)NC2=O)OC(C1O)N1C=NC2=C1C(=S)N=CN2

InChIKey

InChIKey=CLQSRYHBRBUXTM-DXBJRKCQSA-N

Formula

C19H25N6O18P3S

Mass

750.41

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleotides

Subclass

Purine ribonucleotides

Intermediate Tree Nodes

Not available

Direct Parent

Purine ribonucleoside triphosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine ribonucleoside triphosphate - Pyrimidine ribonucleoside triphosphate - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - Monosaccharide phosphate - Purinethione - Imidazopyrimidine - Purine - Monoalkyl phosphate - Pyrimidinethione - Pyrimidone - Hydropyrimidine - Monosaccharide - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Alkyl phosphate - Pyrimidine - Heteroaromatic compound - Oxolane - Vinylogous amide - Azole - Imidazole - Secondary alcohol - Urea - 1,2-diol - Lactam - Oxacycle - Organoheterocyclic compound - Azacycle - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Alcohol - Organonitrogen compound - Organic oxygen compound - Organooxygen compound - Organosulfur compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine ribonucleoside triphosphates. These are purine ribobucleotides with a triphosphate group linked to the ribose moiety.

External Descriptors

Not available

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