Structure Information
Structure

Compound Identification

SMILES

CCN1CC2(COC(=O)c3ccccc3N3C(=O)CCC3=O)CCC(O)C34C5CC6C(OC)C5(O)C(O)(CC6OC)C(O)(CC23)C14

InChIKey

InChIKey=NSUPDHTYRQUZFR-UHFFFAOYSA-N

Formula

C34H44N2O10

Mass

640.73

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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

Aconitane-type diterpenoid alkaloids

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Aconitane-type diterpenoid alkaloid - Acylaminobenzoic acid or derivatives - 1-phenylpyrrolidine - Benzoate ester - Quinolidine - Benzoic acid or derivatives - Alkaloid or derivatives - Benzoyl - Azepane - Monocyclic benzene moiety - Carboxylic acid imide, n-substituted - Piperidine - Pyrrolidone - 2-pyrrolidone - Benzenoid - Carboxylic acid imide - Cyclic alcohol - Dicarboximide - Tertiary alcohol - Pyrrole - Pyrrolidine - Tertiary aliphatic amine - Tertiary amine - Carboxylic acid ester - 1,2-aminoalcohol - Lactam - Amino acid or derivatives - Secondary alcohol - Azacycle - Monocarboxylic acid or derivatives - Ether - Polyol - Dialkyl ether - Carboxylic acid derivative - Organoheterocyclic compound - Amine - Carbonyl group - Organic oxide - Organopnictogen compound - Organic oxygen compound - Alcohol - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as aconitane-type diterpenoid alkaloids. These are alkaloid diterpenoids with a structure based on the hexacyclic aconitane skeleton. These compounds have no oxygen functionality at the C7 atom.

External Descriptors

Not available

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