Compound Identification
SMILES
CC1OC2C(C)C(=O)OC2C1C1CCCCN2C1CCC2=O
InChIKey
InChIKey=KAZLWMNQDDRLDC-UHFFFAOYSA-N
Formula
C17H25NO4
Mass
307.39
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Alkaloids and derivatives
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Class
Stemona alkaloids
- Subclass Parvistemoline-type alkaloids
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Class
Stemona alkaloids
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Superclass
Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Stemona alkaloids
Subclass
Parvistemoline-type alkaloids
Intermediate Tree Nodes
Not available
Direct Parent
Parvistemoline-type alkaloids
Alternative Parents
Pyrroloazepines Furofurans Azepanes Pyrrolidine-2-ones Gamma butyrolactones N-alkylpyrrolidines Tetrahydrofurans Tertiary carboxylic acid amides Carboxylic acid esters Lactams Azacyclic compounds Oxacyclic compounds Dialkyl ethers Monocarboxylic acids and derivatives Carbonyl compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Organopnictogen compounds
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Parvistemoline backbone - Pyrroloazepine - Furofuran - Azepane - Gamma butyrolactone - N-alkylpyrrolidine - 2-pyrrolidone - Pyrrolidone - Pyrrolidine - Tetrahydrofuran - Tertiary carboxylic acid amide - Carboxamide group - Carboxylic acid ester - Lactam - Lactone - Carboxylic acid derivative - Dialkyl ether - Ether - Oxacycle - Azacycle - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Organic oxide - Carbonyl group - Hydrocarbon derivative - Organic oxygen compound - Organopnictogen compound - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Aliphatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as parvistemoline-type alkaloids. These are alkaloids that feature a conserved pyrrolo[1,2-a]azepine nucleus. They are characterized by a hexahydro-2,6-dimethyl-5-oxofuro[3,2-b]furan-3-yl moiety attached to C-9 in the pyrrolo[1,2-a]azepine nucleus.
External Descriptors
Not available