You are using an unsupported browser. Please upgrade your browser to a newer version to get the best experience on ClassyFire.
Structure Information
Structure

Compound Identification

SMILES

C1=CC=CC=C1.CCO[P@]1(=O)OC[C@@H]2O[C@@H]([C@H](O)[C@@H]2O1)N1C=NC2=C1N=CN=C2N

InChIKey

InChIKey=IRTSOWBBYWGRAO-HDEQLFIVSA-N

Formula

C18H22N5O6P

Mass

435.377

Export to:

JSON SDF CSV

Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleotides

Subclass

Cyclic purine nucleotides

Intermediate Tree Nodes

Not available

Direct Parent

3',5'-cyclic purine nucleotides

Alternative Parents

Molecular Framework

Not available

Substituents

3',5'-cyclic purine ribonucleotide - Pentose phosphate - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Monosaccharide phosphate - Imidazopyrimidine - Purine - Aminopyrimidine - N-substituted imidazole - Imidolactam - Benzenoid - Organic phosphoric acid derivative - Pyrimidine - Monosaccharide - Monocyclic benzene moiety - Phosphoric acid ester - Aromatic hydrocarbon - Azole - Imidazole - Heteroaromatic compound - Oxolane - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Amine - Alcohol - Hydrocarbon derivative - Organic oxide - Unsaturated hydrocarbon - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Primary amine - Hydrocarbon - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 3',5'-cyclic purine nucleotides. These are purine nucleotides in which the oxygen atoms linked to the C3 and C5 carbon atoms of the ribose moiety are both bonded the same phosphorus atom of the phosphate group.

External Descriptors

Not available

Previous Back Next