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

InChIKey=JPIFQMSMUJHUBQ-SQTHQVPUSA-N

C22H35NO4

377.525

Organic compounds

Alkaloids and derivatives

Stemona alkaloids

Stemoamide-type alkaloids

Not available

Stichoneurine-type alkaloids

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

Aliphatic heteropolycyclic compounds

Stichoneurine-type alkaloid - Pyrroloazepine - Azepane - Dicarboxylic acid or derivatives - Gamma butyrolactone - N-alkylpyrrolidine - Pyrrolidine - Tetrahydrofuran - Amino acid or derivatives - Carboxylic acid ester - Lactone - Tertiary amine - Tertiary aliphatic amine - Carboxylic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - 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