CC1OC2C(C)C(=O)OC2C1C1CCCCN2C(CCC12)C1CC(C)C(=O)O1

InChIKey=NSVYJHREGGWCHW-UHFFFAOYSA-N

C22H33NO5

391.508

Organic compounds

Alkaloids and derivatives

Stemona alkaloids

Stemoamide-type alkaloids

Not available

Stichoneurine-type alkaloids

Parvistemoline-type alkaloids Pyrroloazepines Furofurans Azepanes N-alkylpyrrolidines Dicarboxylic acids and derivatives Gamma butyrolactones Tetrahydrofurans Trialkylamines Amino acids and derivatives Carboxylic acid esters Oxacyclic compounds Azacyclic compounds Dialkyl ethers Carbonyl compounds Organic oxides Organopnictogen compounds Hydrocarbon derivatives

Aliphatic heteropolycyclic compounds

Stichoneurine-type alkaloid - Parvistemoline backbone - Pyrroloazepine - Furofuran - Azepane - Dicarboxylic acid or derivatives - Gamma butyrolactone - N-alkylpyrrolidine - Pyrrolidine - Tetrahydrofuran - Amino acid or derivatives - Carboxylic acid ester - Lactone - Tertiary aliphatic amine - Tertiary amine - Carboxylic acid derivative - Dialkyl ether - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Organic oxide - Amine - Organopnictogen compound - Hydrocarbon derivative - Organic oxygen compound - Carbonyl group - Organonitrogen compound - Organooxygen compound - Aliphatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as stichoneurine-type alkaloids. These are stemona alkaloids with a structure that typically contains a 3-methyloxolan-2-one and a 5-propyloxolan-2-one moieties that are attached to the characteristic pyrrolo[1,2-a]azepine skeleton at the C3 and C9 position, respectively.

Not available