CC[C@H](C)[C@H](N1C(O)C2=CC(C)=CC(O)=C2C2=C1C(=O)C1=C(C=CC=C1OCC1=CC=CC=C1)C2=O)C(=O)OC(C)(C)C

InChIKey=GHZWQYLWYOFYMV-ZCWIFQGLSA-N

C35H37NO7

583.681

Organic compounds

Alkaloids and derivatives

Protopine alkaloids

Not available

Not available

Protopine alkaloids

Isoleucine and derivatives Phenanthridines and derivatives Alpha amino acid esters Quinoline quinones Naphthoquinones Aryl ketones Quinones Phenol ethers 1-hydroxy-4-unsubstituted benzenoids Fatty acid esters 1-hydroxy-2-unsubstituted benzenoids Alkyl aryl ethers Benzene and substituted derivatives Vinylogous amides Carboxylic acid esters Azacyclic compounds Monocarboxylic acids and derivatives Alkanolamines Hydrocarbon derivatives Organic oxides

Aromatic heteropolycyclic compounds

Protopine skeleton - Phenanthridine - Benzoquinoline - Isoleucine or derivatives - Alpha-amino acid ester - Naphthoquinone - Quinoline quinone - Alpha-amino acid or derivatives - Naphthalene - Quinoline - Aryl ketone - Phenol ether - Quinone - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Fatty acid ester - Alkyl aryl ether - Phenol - Monocyclic benzene moiety - Benzenoid - Fatty acyl - Vinylogous amide - Carboxylic acid ester - Ketone - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Ether - Alkanolamine - Carboxylic acid derivative - Azacycle - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as protopine alkaloids. These are alkaloids with a structure based on a tricyclic protopine formed by oxidative ring fission of protoberberine N-metho salts.

Not available