Compound Identification
SMILES
CC[C@H]1[C@H]2[C@@H](CCCN3C(=CC(=O)[C@@]23O)[C@@H]2C[C@H](C)C(=O)O2)O[C@@]1(C)OC(=O)[C@H](C)CO
InChIKey
InChIKey=LKOXOSQZRBEAJC-UYTGGGRFSA-N
Formula
C23H33NO8
Mass
451.516
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
Ketals Beta hydroxy acids and derivatives Azepanes Gamma butyrolactones Dicarboxylic acids and derivatives Vinylogous amides Tetrahydrofurans Pyrrolines Ketones Carboxylic acid esters Oxacyclic compounds Azacyclic compounds Alkanolamines Primary alcohols Organopnictogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Stemoamide backbone - Ketal - Beta-hydroxy acid - Azepane - Hydroxy acid - Gamma butyrolactone - Dicarboxylic acid or derivatives - Vinylogous amide - Tetrahydrofuran - Pyrroline - Lactone - Ketone - Carboxylic acid ester - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Alkanolamine - Acetal - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Organonitrogen compound - Carbonyl group - 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