Compound Identification
SMILES
CO[C@H]1CC=C2CCN3CCC[C@]4(CO)OC(=O)C=C4[C@]23C1
InChIKey
InChIKey=SSUDSSITGZKVST-XKQJLSEDSA-N
Formula
C17H23NO4
Mass
305.374
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
Indoles and derivatives Azepanes N-alkylpyrrolidines Butenolides Enoate esters Trialkylamines Amino acids and derivatives Lactones Oxacyclic compounds Azacyclic compounds Monocarboxylic acids and derivatives Dialkyl ethers Carbonyl compounds Hydrocarbon derivatives Organic oxides Primary alcohols
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Stemoamide backbone - Indole or derivatives - Azepane - 2-furanone - N-alkylpyrrolidine - Dihydrofuran - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Pyrrolidine - Amino acid or derivatives - Carboxylic acid ester - Lactone - Tertiary aliphatic amine - Tertiary amine - Carboxylic acid derivative - Dialkyl ether - Oxacycle - Ether - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Amine - Hydrocarbon derivative - Alcohol - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Carbonyl group - Organonitrogen compound - Organooxygen compound - Primary alcohol - 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