Structure Information
Structure

Compound Identification

SMILES

CCC1[C@H]2[C@@H](CCCN3[C@@H](CCC23)C2C[C@H](C)C(=O)O2)OC11OC(=O)C(C)=C1

InChIKey

InChIKey=UINUUSQOLRQGNF-PFFOFICLSA-N

Formula

C22H31NO5

Mass

389.492

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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

Aliphatic heteropolycyclic compounds

Substituents

Stichoneurine-type alkaloid - Azepane - Ketal - 2-furanone - Dicarboxylic acid or derivatives - Gamma butyrolactone - N-alkylpyrrolidine - Dihydrofuran - Oxolane - Pyrrolidine - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Amino acid or derivatives - Carboxylic acid ester - Lactone - Tertiary amine - Tertiary aliphatic amine - Carboxylic acid derivative - Oxacycle - Azacycle - Acetal - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Aliphatic 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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