Compound Identification
SMILES
O=C1CC[C@@H]2N1CCCC[C@@]21OC(=O)C=C1
InChIKey
InChIKey=HHIMWJSPIDITHJ-CABZTGNLSA-N
Formula
C12H15NO3
Mass
221.256
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Alkaloids and derivatives
-
Class
Stemona alkaloids
- Subclass Tuberostemospironine-type alkaloids
-
Class
Stemona alkaloids
-
Superclass
Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Stemona alkaloids
Subclass
Tuberostemospironine-type alkaloids
Intermediate Tree Nodes
Not available
Direct Parent
Tuberostemospironine-type alkaloids
Alternative Parents
Pyrroloazepines Azepanes Pyrrolidine-2-ones Butenolides N-alkylpyrrolidines Tertiary carboxylic acid amides Enoate esters Lactams Lactones Azacyclic compounds Oxacyclic compounds Monocarboxylic acids and derivatives Carbonyl compounds Organic oxides Hydrocarbon derivatives Organonitrogen compounds
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Tuberostemospironine backbone - Pyrroloazepine - Azepane - 2-furanone - Pyrrolidone - 2-pyrrolidone - N-alkylpyrrolidine - Dihydrofuran - Pyrrolidine - Tertiary carboxylic acid amide - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Carboxamide group - Carboxylic acid ester - Lactone - Lactam - Oxacycle - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Organic oxide - Aliphatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as tuberostemospironine-type alkaloids. These are alkaloids with a structure that is characterized by a 2H-spiro[furan-2,9A[9H]pyrrolo[1,2-a]azepin]-\n5-one nucleus which displays a spiro gamma-lactone at C-9 of the basic ring.
External Descriptors
Not available