Compound Identification
SMILES
CS(O)(=O)=O.CCN1CCC2=C3C1CCC(C)N3C1=CC=CC=C21
InChIKey
InChIKey=GYJGOPUKUMODSO-UHFFFAOYSA-N
Formula
C18H26N2O3S
Mass
350.48
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 Naphthyridines 3-alkylindoles Aralkylamines Benzenoids Sulfonyls Pyrroles Organosulfonic acids Methanesulfonates Heteroaromatic compounds Alkanesulfonic acids Trialkylamines Azacyclic compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Not available
Substituents
Indolo[3,2-1de][1,5]naphthyridine - Beta-carboline - Pyridoindole - 3-alkylindole - Naphthyridine - Indole - Indole or derivatives - Aralkylamine - Benzenoid - Pyrrole - Methanesulfonate - Alkanesulfonic acid - Sulfonyl - Organosulfonic acid - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Heteroaromatic compound - Tertiary aliphatic amine - Tertiary amine - Azacycle - Organoheterocyclic compound - Organonitrogen compound - Amine - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Organosulfur 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