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Structure Information
Structure

Compound Identification

SMILES

COC1=C(O)C2=C3[C@H](CCC4=CC(OC)=C(OC)C(OC)=C24)N(C(O)C(=O)C3=C1)S(C)(=O)=O

InChIKey

InChIKey=NQNSTIZFOVWHPH-BJDAYTSDSA-N

Formula

C22H25NO9S

Mass

479.5

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Alkaloids and derivatives

Class

Homoaporphines

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Homoaporphines

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Homoaporphine - Isoquinolone - Tetrahydroisoquinoline - Anisole - Phenol ether - Aryl alkyl ketone - Aryl ketone - Alkyl aryl ether - Phenol - Organic sulfonic acid amide - Organosulfonic acid amide - Benzenoid - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Sulfonyl - Ketone - Alkanolamine - Organoheterocyclic compound - Azacycle - Ether - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Organic oxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as homoaporphines. These are alkaloids derived from phenethylisoquinoline precursors by direct intramolecular oxidative coupling. They incorporate a nucleus A and are always pentaoxygenated at C- 1, -2, - 10, - 11, and - 12. The nitrogen function in ring B is usually N-methylated, but it may also be secondary.

External Descriptors

Not available

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