Compound Identification
SMILES
CN(C)[C@@H]1N2C3=CC=CC=C3C3=C2C(=C[C@]11CCOC1=O)N(CC3)C(C)=O
InChIKey
InChIKey=UWACLXLGGVZUIK-TZIWHRDSSA-N
Formula
C21H23N3O3
Mass
365.433
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
- Superclass Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Indolonaphthyridine alkaloids
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Indolonaphthyridine alkaloids
Alternative Parents
Beta carbolines 3-alkylindoles Naphthyridines Aminopyridines and derivatives Benzenoids Gamma butyrolactones Heteroaromatic compounds Acetamides Oxolanes Tertiary carboxylic acid amides Pyrroles Carboxylic acid esters Monocarboxylic acids and derivatives Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Carbonyl compounds Amines Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Indolo[3,2-1de][1,5]naphthyridine - Beta-carboline - Pyridoindole - Naphthyridine - 3-alkylindole - Indole - Indole or derivatives - Aminopyridine - Gamma butyrolactone - Benzenoid - Heteroaromatic compound - Oxolane - Pyrrole - Tertiary carboxylic acid amide - Acetamide - Carboxamide group - Carboxylic acid ester - Lactone - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Oxacycle - Organic oxide - Organooxygen compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Amine - Organonitrogen compound - Carbonyl group - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as indolonaphthyridine alkaloids. These are a numerous and relatively straightforward subgroup of the b-carbolines, e.g. Canthin-6-one, in which an additional C3 unit is attached between C-1 and the indole nitrogen to form an additional ring. The group includes a few dimeric examples, such as Haplophytine.
External Descriptors
Not available