Compound Identification
SMILES
CN1C2=CC=CC=C2C2=C1[C@@H]1C[C@@H]3[C@@H](CO[C@](C)(O)[C@@H]3CC(=O)C3=CC=CO3)[C@H](C2)N1C
InChIKey
InChIKey=YVYNTJLGNMGSJB-TWWBAOOUSA-N
Formula
C26H30N2O4
Mass
434.536
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Alkaloids and derivatives
- Class Macroline alkaloids
-
Superclass
Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Macroline alkaloids
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Macroline alkaloids
Alternative Parents
Beta carbolines 3-alkylindoles N-alkylindoles Aryl alkyl ketones Aralkylamines Piperidines Oxanes N-methylpyrroles Benzenoids Heteroaromatic compounds Furans Trialkylamines Hemiacetals Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Macroline skeleton - Beta-carboline - Pyridoindole - N-alkylindole - 3-alkylindole - Indole - Indole or derivatives - Aryl ketone - Aryl alkyl ketone - Aralkylamine - N-methylpyrrole - Oxane - Piperidine - Substituted pyrrole - Benzenoid - Furan - Pyrrole - Heteroaromatic compound - Tertiary aliphatic amine - Tertiary amine - Hemiacetal - Ketone - Organoheterocyclic compound - Azacycle - Oxacycle - Hydrocarbon derivative - Amine - Organic oxide - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as macroline alkaloids. These are alkaloids with a structure that is based on the tetracyclic macroline skeleton. The macroline skeleton arises by scission of the C-21 to N-4 bond of the akuammilan skeleton, and mostly occurs in bisindole alkaloids.
External Descriptors
Not available