Structure Information
Structure

Compound Identification

SMILES

CN1C2=CC=CC=C2C2=C1[C@@H]1C[C@@H]3[C@@H](CO[C@](C)(O)[C@@H]3CC(=O)C3=CC=CO3)[C@H](C2)N1C

InChIKey

InChIKey=YVYNTJLGNMGSJB-TWWBAOOUSA-N

Formula

C26H30N2O4

Mass

434.536

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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 - Beta-carboline - Pyridoindole - N-alkylindole - 3-alkylindole - Indole - Indole or derivatives - Aryl ketone - Aryl alkyl ketone - Aralkylamine - N-methylpyrrole - Oxane - Piperidine - Substituted pyrrole - Benzenoid - Furan - Pyrrole - Heteroaromatic compound - Tertiary aliphatic amine - Tertiary amine - Hemiacetal - Ketone - Organoheterocyclic compound - Azacycle - Oxacycle - Hydrocarbon derivative - Amine - Organic oxide - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - 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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