Structure Information
Structure

Compound Identification

SMILES

C[C@H]1C[C@H](OC1=O)c1ccc2[C@H](CCCCn12)[C@@H]1[C@H](C)O[C@@H]2[C@H](C)C(=O)O[C@H]12

InChIKey

InChIKey=BCTUHTLEKUMPLL-ZHGGVEMFSA-N

Formula

C22H29NO5

Mass

387.476

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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 - Furofuran - Azepine - Substituted pyrrole - Gamma butyrolactone - Dicarboxylic acid or derivatives - Heteroaromatic compound - Tetrahydrofuran - Pyrrole - Lactone - Carboxylic acid ester - Oxacycle - Azacycle - Organoheterocyclic compound - Ether - Dialkyl ether - Carboxylic acid derivative - 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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