[H][C@]1(C)C[C@]([H])(OC1=O)[C@]1([H])C[C@@]2([H])[C@]3([H])N1CCCC[C@]3([H])[C@@]([H])(CC=C)[C@]1([H])OC(=O)C([H])(C)[C@]21[H]

InChIKey=KESNDIVRNVSOTE-XOBIQDLYSA-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 Dicarboxylic acids and derivatives Gamma butyrolactones N-alkylpyrrolidines Tetrahydrofurans Amino acids and derivatives Trialkylamines Carboxylic acid esters Oxacyclic compounds Azacyclic compounds Carbonyl compounds Organopnictogen compounds Hydrocarbon derivatives Organic oxides

Aliphatic heteropolycyclic compounds

Stichoneurine-type alkaloid - Stenine backbone - Indole or derivatives - 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 - Organooxygen compound - Organonitrogen compound - Organic oxide - 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