C[C@H]1OC[C@H]2[C@@H]3NC4=CC=CC=C4C33CCN4[C@H]3C[C@H]2[C@H]1[C@@H]4\C=C\C1=CN2CCC34[C@@H]2C[C@@H]1[C@@H](CO)[C@@H]3NC1=CC=CC=C41

InChIKey=FMNWIRPKXNZZBL-ZBXSNBANSA-N

C38H44N4O2

588.796

Organic compounds

Alkaloids and derivatives

Strychnos alkaloids

Not available

Not available

Strychnos alkaloids

Yohimbine alkaloids Carbazoles Indolines Indolizidines Aralkylamines Secondary alkylarylamines Tetrahydropyridines Piperidines Oxanes N-alkylpyrrolidines Benzenoids 1,3-aminoalcohols Trialkylamines Oxacyclic compounds Allylamines Enamines Dialkyl ethers Azacyclic compounds Primary alcohols Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Strychnan skeleton - Akuammicine-skeleton - Yohimbine alkaloid - Yohimban skeleton - Stemmadenine-skeleton - Carbazole - Indole or derivatives - Dihydroindole - Indolizidine - Secondary aliphatic/aromatic amine - Aralkylamine - Tetrahydropyridine - Oxane - Piperidine - Benzenoid - N-alkylpyrrolidine - Pyrrolidine - 1,3-aminoalcohol - Tertiary aliphatic amine - Tertiary amine - Organoheterocyclic compound - Azacycle - Secondary amine - Oxacycle - Dialkyl ether - Enamine - Ether - Allylamine - Primary alcohol - Organic oxygen compound - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Amine - Alcohol - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as strychnos alkaloids. These are alkaloids having a core structure based on the strychnan, stemmadenine (seco-curan), or the akuammicine (curan) skeleton.

Not available