Compound Identification
SMILES
CC[C@H]1[C@@H]2OC(=O)[C@@H](C)[C@@H]2[C@]23CCN4CCCC[C@]1(O2)[C@]34O
InChIKey
InChIKey=OOPWKRQLSGPZSK-UAKWQSKWSA-N
Formula
C17H25NO4
Mass
307.39
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Alkaloids and derivatives
-
Class
Stemona alkaloids
- Subclass Stenine-type alkaloids
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Class
Stemona alkaloids
-
Superclass
Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Stemona alkaloids
Subclass
Stenine-type alkaloids
Intermediate Tree Nodes
Not available
Direct Parent
Stenine-type alkaloids
Alternative Parents
Indoles and derivatives 1,4-oxazepines Azepanes Oxanes N-alkylpyrrolidines Gamma butyrolactones Tetrahydrofurans Oxetanes Hemiaminals Cyclic alcohols and derivatives Carboxylic acid esters Oxacyclic compounds Azacyclic compounds Monocarboxylic acids and derivatives Dialkyl ethers Carbonyl compounds Hydrocarbon derivatives Organic oxides Organopnictogen compounds
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Stenine backbone - Indole or derivatives - Para-oxazepine - Azepane - Gamma butyrolactone - N-alkylpyrrolidine - Oxane - Cyclic alcohol - Tetrahydrofuran - Pyrrolidine - Carboxylic acid ester - Hemiaminal - Lactone - Oxetane - Alkanolamine - Carboxylic acid derivative - Dialkyl ether - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Organic nitrogen compound - Organic oxygen compound - Hydrocarbon derivative - Carbonyl group - Organopnictogen compound - Organic oxide - Organonitrogen compound - Organooxygen compound - Aliphatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as stenine-type alkaloids. These are alkaloids which can be structurally represented by the tetracyclic\nfuro[2,3-h]pyrrolo[3,2,1-jk][1]benzazepin-10(2H)-one nucleus.
External Descriptors
Not available