Compound Identification
SMILES
COC(=O)[C@@H]1[C@H]2C[C@@H]3N(CC[C@@H]4C5=CC=CC=C5N1[C@]34C1=C(OC)C=C3N(C)[C@H]4[C@@H]5C[C@@H]6[C@@H](C(=O)OC)[C@]4(CCN5C\C6=C\C)C3=C1)C\C2=C\C
InChIKey
InChIKey=HTZWAUOEBYTKSR-HHRSCMRWSA-N
Formula
C42H50N4O5
Mass
690.885
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Alkaloids and derivatives
- Class Pleiocarpaman alkaloids
-
Superclass
Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Pleiocarpaman alkaloids
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Pleiocarpaman alkaloids
Alternative Parents
Lignans, neolignans and related compounds Indolonaphthyridine alkaloids Alpha amino acid esters Beta carbolines Carbazoles Quinolizidines Naphthyridines Piperidinecarboxylic acids Anisoles Dialkylarylamines Alkyl aryl ethers Aralkylamines Dicarboxylic acids and derivatives Methyl esters Trialkylamines Azacyclic compounds Hydrocarbon derivatives Organic oxides Carbonyl compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Pleiocarpaman skeleton - Neolignan skeleton - Indolo[3,2-1de][1,5]naphthyridine - Pyridoindole - Alpha-amino acid ester - Carbazole - Beta-carboline - Quinolizidine - Alpha-amino acid or derivatives - Naphthyridine - Piperidinecarboxylic acid - Indole or derivatives - Phenol ether - Dialkylarylamine - Tertiary aliphatic/aromatic amine - Anisole - Alkyl aryl ether - Aralkylamine - Dicarboxylic acid or derivatives - Benzenoid - Piperidine - Methyl ester - Tertiary amine - Tertiary aliphatic amine - Amino acid or derivatives - Carboxylic acid ester - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Ether - Organonitrogen compound - Organic oxide - Hydrocarbon derivative - Organic oxygen compound - Carbonyl group - Organooxygen compound - Amine - Organic nitrogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as pleiocarpaman alkaloids. These are alkaloids with a structure that is based on the pleiocarpaman skeleton. These alkaloids arise from the cyclization of a corynantheine precursor via C-16 to N-1.
External Descriptors
Not available