Compound Identification
SMILES
[H][C@]1(CO)O[C@@]([H])(OC2=C(C3=C(C=CN3C)C=C2)C2=CC3=C(OCO3)C=C2CO)[C@]([H])(O)[C@@]([H])(O)[C@]1([H])O
InChIKey
InChIKey=MNBXTLGGZVLCRP-LDBVRRDLSA-N
Formula
C23H25NO9
Mass
459.451
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
- Superclass Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Amaryllidaceae alkaloids
Subclass
Galanthindole-type amaryllidaceae alkaloids
Intermediate Tree Nodes
Not available
Direct Parent
Galanthindole-type amaryllidaceae alkaloids
Alternative Parents
Phenolic glycosides Hexoses O-glycosyl compounds N-alkylindoles Benzodioxoles Indoles Benzenoids Oxanes N-methylpyrroles Heteroaromatic compounds Secondary alcohols Azacyclic compounds Polyols Acetals Oxacyclic compounds Aromatic alcohols Hydrocarbon derivatives Primary alcohols Organonitrogen compounds Organopnictogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Galanthindole-type amaryllidaceae alkaloid - Phenolic glycoside - Hexose monosaccharide - Glycosyl compound - O-glycosyl compound - N-alkylindole - Benzodioxole - Indole - Indole or derivatives - Monosaccharide - N-methylpyrrole - Benzenoid - Oxane - Substituted pyrrole - Heteroaromatic compound - Pyrrole - Secondary alcohol - Polyol - Organoheterocyclic compound - Azacycle - Oxacycle - Acetal - Primary alcohol - Aromatic alcohol - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Alcohol - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as galanthindole-type amaryllidaceae alkaloids. These are amaryllidaceae alkaloids based on a 7-arylindole or 7-aryl-2,3-dihydroindole skeleton.
External Descriptors
Not available