Compound Identification
SMILES
COC(=O)[C@H]1CC(=O)N2C3=C(C=C(Cl)C=C3)C3=C2[C@H]1NCC3
InChIKey
InChIKey=UUBIPWORYDNUGD-FZMZJTMJSA-N
Formula
C16H15ClN2O3
Mass
318.76
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 Aralkylamines Aryl chlorides Benzenoids Pyrroles Methyl esters Heteroaromatic compounds Amino acids and derivatives Lactams Monocarboxylic acids and derivatives Azacyclic compounds Dialkylamines Hydrocarbon derivatives Organic oxides Organochlorides Carbonyl compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Indolo[3,2-1de][1,5]naphthyridine - Beta-carboline - Pyridoindole - Naphthyridine - 3-alkylindole - Indole - Indole or derivatives - Aralkylamine - Aryl chloride - Aryl halide - Benzenoid - Heteroaromatic compound - Methyl ester - Pyrrole - Amino acid or derivatives - Carboxylic acid ester - Lactam - Secondary amine - Carboxylic acid derivative - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Secondary aliphatic amine - Azacycle - Organochloride - Hydrocarbon derivative - Amine - Organohalogen compound - Carbonyl group - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - 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