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Structure Information
Structure

Compound Identification

SMILES

COC(=O)C1(C[O-])C2CC3C4=C(CC1[N+]3(C)C\C2=C\C)C1=C(N4C)C(OC)=CC=C1

InChIKey

InChIKey=NOGSEKYKSJBDKV-NSIKDUERSA-N

Formula

C24H30N2O4

Mass

410.514

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Alkaloids and derivatives

Class

Macroline alkaloids

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Macroline alkaloids

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Macroline skeleton - Corynanthean skeleton - Vobasan skeleton - Pyridoindole - Beta-carboline - N-alkylindole - 3-alkylindole - Indole - Indole or derivatives - Piperidinecarboxylic acid - Quinuclidine - Anisole - Phenol ether - Alkyl aryl ether - Aralkylamine - Benzenoid - Piperidine - Substituted pyrrole - N-methylpyrrole - Tetraalkylammonium salt - Heteroaromatic compound - Methyl ester - Pyrrole - Quaternary ammonium salt - Carboxylic acid ester - Carboxylic acid derivative - Ether - Monocarboxylic acid or derivatives - Azacycle - Organoheterocyclic compound - Amine - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Organic salt - Alkoxide - Carbonyl group - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organic zwitterion - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as macroline alkaloids. These are alkaloids with a structure that is based on the tetracyclic macroline skeleton. The macroline skeleton arises by scission of the C-21 to N-4 bond of the akuammilan skeleton, and mostly occurs in bisindole alkaloids.

External Descriptors

Not available

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