Structure Information
Structure

Compound Identification

SMILES

C[C@H](CC1=CC=CC=C1)NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H]2COP(O)(=O)O[C@@H]2[C@H]1O

InChIKey

InChIKey=MKYZONTUKKUGCB-OCXLHJLWSA-N

Formula

C19H22N5O6P

Mass

447.388

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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

Aromatic heteropolycyclic compounds

Substituents

3',5'-cyclic purine ribonucleotide - Pentose phosphate - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Amphetamine or derivatives - Monosaccharide phosphate - Imidazopyrimidine - Phenylpropane - Purine - Aminopyrimidine - Secondary aliphatic/aromatic amine - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Organic phosphoric acid derivative - Imidolactam - Benzenoid - Pyrimidine - Oxolane - Azole - Heteroaromatic compound - Imidazole - Secondary alcohol - Secondary amine - Oxacycle - Organoheterocyclic compound - Azacycle - Organic nitrogen compound - Alcohol - Organooxygen compound - Amine - Organic oxide - Organic oxygen compound - Organonitrogen compound - Hydrocarbon derivative - 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

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