Structure Information
Structure

Compound Identification

SMILES

[H][C@@]1(C)CC[C@]2(C)C([H])(CC[C@]3(C)[C@@]([H])(C)[C@@]([H])(O)CCC23[H])[C@@]1(C)CC1=CNC2=C1C=CC(O)=C2

InChIKey

InChIKey=NWKNHNUJGTXAFZ-GVRCUDJHSA-N

Formula

C28H41NO2

Mass

423.641

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Lipids and lipid-like molecules

Class

Prenol lipids

Subclass

Diterpenoids

Intermediate Tree Nodes

Not available

Direct Parent

Colensane and clerodane diterpenoids

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Clerodane diterpenoid - Hydrophenanthrene - Phenanthrene - Hydroxyindole - 3-alkylindole - Indole - Indole or derivatives - 1-hydroxy-2-unsubstituted benzenoid - Benzenoid - Substituted pyrrole - Cyclic alcohol - Heteroaromatic compound - Pyrrole - Secondary alcohol - Azacycle - Organoheterocyclic compound - Alcohol - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as colensane and clerodane diterpenoids. These are diterpenoids with a structure based on the clerodane or the colensane skeleton. Clerodanes arise from labdanes by two methyl migrations.

External Descriptors

Not available

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