Compound Identification
SMILES
C[C@@H]1[C@H](O[C@@H]2CCCN3CCC[C@H]3[C@@H]12)[C@@H]1OC(=O)C(C)=C1
InChIKey
InChIKey=ROFRWHNTTQEGIC-IJOLSIAMSA-N
Formula
C17H25NO3
Mass
291.391
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 N-alkylpyrrolidines Butenolides Oxolanes Enoate esters Trialkylamines Lactones Amino acids and derivatives Oxacyclic compounds Monocarboxylic acids and derivatives Dialkyl ethers Azacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Stemoamide backbone - Azepane - 2-furanone - N-alkylpyrrolidine - Dihydrofuran - Oxolane - Pyrrolidine - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Amino acid or derivatives - Carboxylic acid ester - Lactone - Tertiary amine - Tertiary aliphatic amine - Monocarboxylic acid or derivatives - Ether - Dialkyl ether - Carboxylic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic oxide - Amine - Carbonyl group - Organic nitrogen compound - Organic oxygen compound - 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