Structure Information
Structure

Compound Identification

SMILES

[H]C([H])([H])C1([H])C(=O)OC([H])(C1([H])[H])C1([H])C([H])([H])C([H])([H])C2([H])C([H])(C([H])([H])C([H])([H])C([H])([H])C([H])([H])[N+]12[H])C1([H])C([H])(OC2([H])C([H])(C(=O)OC12[H])C([H])([H])[H])C([H])([H])[H]

InChIKey

InChIKey=NSVYJHREGGWCHW-UHFFFAOYSA-O

Formula

C22H34NO5

Mass

392.515

Export to:

JSON SDF CSV

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 - Parvistemoline backbone - Pyrroloazepine - Furofuran - Azepane - N-alkylpyrrolidine - Gamma butyrolactone - Dicarboxylic acid or derivatives - Tetrahydrofuran - Pyrrolidine - Tertiary aliphatic amine - Tertiary amine - Lactone - Carboxylic acid ester - Amino acid or derivatives - 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 - Amine - Organic cation - 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

Previous Back Next