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Structure Information
Structure

Compound Identification

SMILES

COC1=C(OC)C=C2C(=C1)N(C1CC3CCN(C)CCC21C(=O)C3(O)C(C)O)C(C)=O

InChIKey

InChIKey=CMRDCKYJDPIYRC-UHFFFAOYSA-N

Formula

C23H32N2O6

Mass

432.517

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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 - Aralkylamine - Acyloin - Benzenoid - Cyclic alcohol - Tertiary alcohol - Tertiary carboxylic acid amide - Acetamide - Amino acid or derivatives - Tertiary amine - Ketone - Tertiary aliphatic amine - Secondary alcohol - 1,2-diol - Carboxamide group - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Ether - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Amine - Alcohol - Organooxygen compound - Organopnictogen compound - Organonitrogen compound - 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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