Structure Information
Structure

Compound Identification

SMILES

CCC1[C@H]2[C@@H](CCCn3c(ccc23)[C@@H]2C[C@H](C)C(=O)O2)O[C@]11OC(=O)C(C)=C1

InChIKey

InChIKey=KKSONBBSOWYZHQ-VQYLNPHBSA-N

Formula

C22H27NO5

Mass

385.46

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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 - Ketal - Azepine - Substituted pyrrole - Gamma butyrolactone - Dicarboxylic acid or derivatives - 2-furanone - Heteroaromatic compound - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Tetrahydrofuran - Pyrrole - Dihydrofuran - Lactone - Carboxylic acid ester - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Acetal - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - 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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