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Structure Information
Structure

Compound Identification

SMILES

COC1C2OP(O)(=O)OCC2OC1N1C=NC2=C1N=C(SC1=CC=C(C=C1)C(C)C)N=C2N

InChIKey

InChIKey=WFFVDTXQFYOEGF-UHFFFAOYSA-N

Formula

C20H24N5O6PS

Mass

493.47

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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 - Diarylthioether - Monosaccharide phosphate - 6-aminopurine - Phenylpropane - Imidazopyrimidine - Cumene - Purine - Aryl thioether - Thiophenol ether - Aminopyrimidine - Organic phosphoric acid derivative - N-substituted imidazole - Monosaccharide - Monocyclic benzene moiety - Pyrimidine - Benzenoid - Imidolactam - Oxolane - Azole - Heteroaromatic compound - Imidazole - Oxacycle - Azacycle - Organoheterocyclic compound - Dialkyl ether - Ether - Sulfenyl compound - Thioether - Organic oxygen compound - Amine - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Primary amine - Organosulfur compound - Organooxygen compound - Organonitrogen compound - 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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