[O-]S([O-])(=O)=O.CC[C@@]12CCCN3CCC4=C([C@H]13)N(C1=CC=CC=C41)[C@](O)(C2)C(=O)OC

InChIKey=NYLMYCHXIHMDRS-YAFGAGFVSA-L

C21H26N2O7S

450.51

Organic compounds

Alkaloids and derivatives

Eburnan-type alkaloids

Not available

Not available

Eburnan-type alkaloids

Indolonaphthyridine alkaloids Beta carbolines 3-alkylindoles Alpha amino acids and derivatives Naphthyridines Aralkylamines Piperidines Benzenoids Organic sulfate salts Methyl esters Pyrroles Heteroaromatic compounds Organic sulfuric acids and derivatives Trialkylamines Alkanolamines Azacyclic compounds Monocarboxylic acids and derivatives Hydrocarbon derivatives Carbonyl compounds Organic oxides Organic anions

Aromatic heteropolycyclic compounds

Eburna alkaloid - Indolo[3,2-1de][1,5]naphthyridine - Beta-carboline - Pyridoindole - Naphthyridine - 3-alkylindole - Alpha-amino acid or derivatives - Indole - Indole or derivatives - Aralkylamine - Organic sulfate salt - Benzenoid - Piperidine - Heteroaromatic compound - Organic sulfuric acid or derivatives - Methyl ester - Pyrrole - Amino acid or derivatives - Carboxylic acid ester - Tertiary aliphatic amine - Tertiary amine - Alkanolamine - Organoheterocyclic compound - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Azacycle - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organic oxygen compound - Amine - Organic anion - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as eburnan-type alkaloids. These are alkaloids with a structure based on the eburnan skeleton, that arises from rearrangement of the aspidospermidine ring system, involving migration of C-21 from C-7 to C-2, fission of the 2,16-bond, and attachment of C-16 to N-1.

Not available