Compound Identification
SMILES
O=C1C[C@H]2[C@H](CCCN3[C@H]2CCC3=O)O1
InChIKey
InChIKey=RQKQXDRKITZZLF-VGMNWLOBSA-N
Formula
C11H15NO3
Mass
209.245
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Alkaloids and derivatives
-
Class
Stemona alkaloids
- Subclass Stemoamide-type alkaloids
-
Class
Stemona alkaloids
-
Superclass
Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Stemona alkaloids
Subclass
Stemoamide-type alkaloids
Intermediate Tree Nodes
Not available
Direct Parent
Stemoamide-type alkaloids
Alternative Parents
Azepanes Pyrrolidine-2-ones Gamma butyrolactones N-alkylpyrrolidines Tertiary carboxylic acid amides Oxolanes Amino acids and derivatives Tertiary amines Carboxylic acid esters Lactams Oxacyclic compounds Azacyclic compounds Monocarboxylic acids and derivatives Hydrocarbon derivatives Carbonyl compounds Organic oxides
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Stemoamide backbone - Azepane - Gamma butyrolactone - Pyrrolidone - 2-pyrrolidone - N-alkylpyrrolidine - Oxolane - Pyrrolidine - Tertiary carboxylic acid amide - Amino acid or derivatives - Carboxamide group - Carboxylic acid ester - Lactam - Lactone - Tertiary amine - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Carbonyl group - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Amine - Aliphatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as stemoamide-type alkaloids. These are alkaloids which include a tricyclic 2H-furo[3,2-c]pyrrolo[1,2-a]azepine nucleus.
External Descriptors
Not available