Structure Information
Structure

Compound Identification

SMILES

CON1C2=NC=NC3=C2N(CC[C@]1(C)CC[C@@]1(C)[C@H](C)CC[C@@]2(C)[C@@H]1CCCC2=C)C(=O)N3C

InChIKey

InChIKey=WUJLQYOSWFQWEL-XWPWZHHHSA-N

Formula

C27H41N5O2

Mass

467.658

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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 - 6-alkylaminopurine - Pyrimidodiazepine - Purinone - Imidazopyrimidine - Purine - Para-diazepine - N-substituted imidazole - Imidolactam - Pyrimidine - Azole - Imidazole - Heteroaromatic compound - Urea - Azacycle - N-organohydroxylamine - Organoheterocyclic compound - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organic oxygen 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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