Compound Identification
SMILES
OC1COC(OCC2OC(Oc3cnc4ccc(=O)n5c6ccccc6c3c45)C(O)C(O)C2O)C(O)C1O
InChIKey
InChIKey=PDYICIGELWDBMF-UHFFFAOYSA-N
Formula
C25H26N2O11
Mass
530.486
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 Disaccharides O-glycosyl compounds Naphthyridines Indoles Indolizines Pyridinones Benzenoids Oxanes Pyrroles Heteroaromatic compounds Lactams Secondary alcohols Oxacyclic compounds Azacyclic compounds Polyols Acetals Organopnictogen compounds Hydrocarbon derivatives Organonitrogen compounds Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Indolo[3,2-1de][1,5]naphthyridine - Beta-carboline - Pyridoindole - Disaccharide - Glycosyl compound - O-glycosyl compound - Diazanaphthalene - Naphthyridine - Indole - Indole or derivatives - Indolizine - Pyrrolopyridine - Pyridinone - Benzenoid - Pyridine - Oxane - Pyrrole - Heteroaromatic compound - Secondary alcohol - Lactam - Organoheterocyclic compound - Acetal - Polyol - Oxacycle - Azacycle - Alcohol - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic nitrogen compound - Organic oxygen 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