C[C@@H]1O[C@@H]2[C@H](C)C(=O)O[C@@H]2[C@@H]1[C@H]1CCCCN2[C@@H](CC[C@@H]12)[C@@H]1C[C@H](C)C(=O)O1

InChIKey=NSVYJHREGGWCHW-FSDFIUDMSA-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 Dicarboxylic acids and derivatives N-alkylpyrrolidines Gamma butyrolactones Oxolanes Amino acids and derivatives Trialkylamines Carboxylic acid esters Dialkyl ethers Azacyclic compounds Oxacyclic compounds Carbonyl compounds Organic oxides Hydrocarbon derivatives

Aliphatic heteropolycyclic compounds

Stichoneurine-type alkaloid - Parvistemoline backbone - Pyrroloazepine - Furofuran - Azepane - Dicarboxylic acid or derivatives - Gamma butyrolactone - N-alkylpyrrolidine - Pyrrolidine - Oxolane - Amino acid or derivatives - Carboxylic acid ester - Lactone - Tertiary aliphatic amine - Tertiary amine - Carboxylic acid derivative - Dialkyl ether - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Hydrocarbon derivative - Amine - Organic oxide - Organic nitrogen compound - 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