CS(O)(=O)=O.CC[C@@]12CCCN3CCC4=C([C@H]13)N(C1=CC=CC=C41)C(=C2)C(=O)OC1CC(C)CC(C)(C)C1

InChIKey=BCHXUZSLWSFIKB-MBLZCJMFSA-N

C30H42N2O5S

542.74

Organic compounds

Alkaloids and derivatives

Eburnan-type alkaloids

Not available

Not available

Eburnan-type alkaloids

Indolonaphthyridine alkaloids Beta carbolines Alpha amino acids and derivatives 3-alkylindoles Naphthyridines Aralkylamines Benzenoids Piperidines Sulfonyls Pyrroles Organosulfonic acids Methanesulfonates Alkanesulfonic acids Heteroaromatic compounds Enoate esters Trialkylamines Azacyclic compounds Monocarboxylic acids and derivatives Carbonyl compounds Hydrocarbon derivatives Organic oxides

Not available

Eburna alkaloid - Indolo[3,2-1de][1,5]naphthyridine - Beta-carboline - Pyridoindole - Alpha-amino acid or derivatives - Naphthyridine - 3-alkylindole - Indole - Indole or derivatives - Aralkylamine - Piperidine - Benzenoid - Alpha,beta-unsaturated carboxylic ester - Alkanesulfonic acid - Enoate ester - Heteroaromatic compound - Sulfonyl - Organosulfonic acid - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Pyrrole - Methanesulfonate - Tertiary aliphatic amine - Amino acid or derivatives - Carboxylic acid ester - Tertiary amine - Azacycle - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Carboxylic acid derivative - Hydrocarbon derivative - Organic oxide - Amine - Carbonyl group - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic nitrogen compound - 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