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Structure Information
Structure

Compound Identification

SMILES

[H]\C(C)=C1\C(=O)[C@@]23CCN(C)CC[C@]1([H])C[C@@]2([H])N(C(C)=O)C1=C3C=CC(OC)=C1O

InChIKey

InChIKey=HXWIJPIEAIUMKA-ZHEWFFLKSA-N

Formula

C22H28N2O4

Mass

384.476

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Alkaloids and derivatives

Class

Condylocarpan alkaloids

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Condylocarpan alkaloids

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Condylocarpan skeleton - Carbazole - Indole or derivatives - Anisole - Alkyl aryl ether - 1-hydroxy-4-unsubstituted benzenoid - Aralkylamine - Benzenoid - Tertiary carboxylic acid amide - Acetamide - Amino acid or derivatives - Carboxamide group - Ketone - Tertiary amine - Tertiary aliphatic amine - Ether - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organic oxide - Amine - Carbonyl group - Organopnictogen compound - Organic oxygen compound - Hydrocarbon derivative - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as condylocarpan alkaloids. These are alkaloids with a structure based on the condylocarpan backbone. These alkaloids contain a ring system similar to that of the curan group, but are formed by cyclisation of C-21 on to C-7 in a Corynanthe precursor, rather than the formation of a 3,7 bond.

External Descriptors

Not available

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