C[C@@H]1O[C@@H]2[C@H](C)C(=O)O[C@@H]2[C@@H]1[C@H]1CCCCN2[C@H]1CCC2=O

InChIKey=KAZLWMNQDDRLDC-FZLLIAENSA-N

C17H25NO4

307.39

Organic compounds

Alkaloids and derivatives

Stemona alkaloids

Parvistemoline-type alkaloids

Not available

Parvistemoline-type alkaloids

Pyrroloazepines Furofurans Azepanes Pyrrolidine-2-ones N-alkylpyrrolidines Gamma butyrolactones Tetrahydrofurans Tertiary carboxylic acid amides Lactams Carboxylic acid esters Oxacyclic compounds Monocarboxylic acids and derivatives Dialkyl ethers Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aliphatic heteropolycyclic compounds

Parvistemoline backbone - Pyrroloazepine - Furofuran - Azepane - N-alkylpyrrolidine - 2-pyrrolidone - Pyrrolidone - Gamma butyrolactone - Tetrahydrofuran - Tertiary carboxylic acid amide - Pyrrolidine - Lactone - Lactam - Carboxylic acid ester - Carboxamide group - Oxacycle - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Ether - Dialkyl ether - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic heteropolycyclic compound

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.

Not available