Structure Information
Structure

Compound Identification

SMILES

CC[C@H]1[C@H]2OC(=O)[C@@H](C)[C@H]2C2=C3[C@H]1CCCCN3C(=C2)[C@H]1C[C@H](C)C(=O)O1

InChIKey

InChIKey=RFGMIDHPFYCJDM-BMVOVXEMSA-N

Formula

C22H29NO4

Mass

371.477

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Alkaloids and derivatives

Class

Stemona alkaloids

Subclass

Stemoamide-type alkaloids

Intermediate Tree Nodes

Not available

Direct Parent

Stichoneurine-type alkaloids

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Stichoneurine-type alkaloid - Pyrroloazepine - Indole or derivatives - Azepine - Dicarboxylic acid or derivatives - Gamma butyrolactone - Substituted pyrrole - Oxolane - Pyrrole - Heteroaromatic compound - Lactone - Carboxylic acid ester - Carboxylic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Carbonyl group - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as stichoneurine-type alkaloids. These are stemona alkaloids with a structure that typically contains a 3-methyloxolan-2-one and a 5-propyloxolan-2-one moieties that are attached to the characteristic pyrrolo[1,2-a]azepine skeleton at the C3 and C9 position, respectively.

External Descriptors

Not available

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