C\C=C\[C@H]1[C@@H]2OC(=O)C(C)[C@@H]2[C@H]2C[C@@H]([C@@H]3C[C@H](C)C(=O)O3)N3CCCC[C@H]1[C@H]23

InChIKey=FSTDHQGAFMTHOW-ZNZHFPFTSA-N

C23H33NO4

387.52

Organic compounds

Alkaloids and derivatives

Stemona alkaloids

Stemoamide-type alkaloids

Not available

Stichoneurine-type alkaloids

Stenine-type alkaloids Indoles and derivatives Azepanes N-alkylpyrrolidines Gamma butyrolactones Dicarboxylic acids and derivatives Oxolanes Trialkylamines Carboxylic acid esters Amino acids and derivatives Oxacyclic compounds Azacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aliphatic heteropolycyclic compounds

Stichoneurine-type alkaloid - Stenine backbone - Indole or derivatives - Azepane - Dicarboxylic acid or derivatives - Gamma butyrolactone - N-alkylpyrrolidine - Oxolane - Pyrrolidine - Amino acid or derivatives - Carboxylic acid ester - Lactone - Tertiary amine - Tertiary aliphatic amine - Carboxylic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Amine - Organic nitrogen compound - Carbonyl group - 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