Compound Identification
SMILES
CC1C(=O)O[C@@H]2CCCN3[C@@H](CCC3=O)[C@]12Br
InChIKey
InChIKey=GSPIVXBGUXTGJB-MPGRNQODSA-N
Formula
C12H16BrNO3
Mass
302.168
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Alkaloids and derivatives
-
Class
Stemona alkaloids
- Subclass Stemoamide-type alkaloids
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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 Carboxylic acid esters Lactams Azacyclic compounds Oxacyclic compounds Monocarboxylic acids and derivatives Organobromides Organonitrogen compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Alkyl bromides
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Stemoamide backbone - Azepane - Gamma butyrolactone - N-alkylpyrrolidine - 2-pyrrolidone - Pyrrolidone - Oxolane - Tertiary carboxylic acid amide - Pyrrolidine - Carboxamide group - Carboxylic acid ester - Lactam - Lactone - Carboxylic acid derivative - Oxacycle - Azacycle - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Organic nitrogen compound - Alkyl halide - Alkyl bromide - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organohalogen compound - Organobromide - Organonitrogen compound - Organooxygen compound - Carbonyl group - 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