Compound Identification
SMILES
CC1=C(CC2=CC=CC=C2)C2=C(N1)[C@@H]1OC3=C(O)C=CC4=C3C11CCN(CC3CC3)C(C4)[C@]1(O)C2
InChIKey
InChIKey=PTRLFMOZDQWPIS-FKKYHJNPSA-N
Formula
C30H32N2O3
Mass
468.597
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Alkaloids and derivatives
- Class Morphinans
-
Superclass
Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Morphinans
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Morphinans
Alternative Parents
Phenanthrenes and derivatives Tetralins Indoles and derivatives Coumarans 1-hydroxy-2-unsubstituted benzenoids Alkyl aryl ethers Aralkylamines Substituted pyrroles Piperidines Benzene and substituted derivatives Tertiary alcohols Heteroaromatic compounds Trialkylamines 1,2-aminoalcohols Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Morphinan - Phenanthrene - Tetralin - Indole or derivatives - Coumaran - Alkyl aryl ether - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Aralkylamine - Monocyclic benzene moiety - Benzenoid - Piperidine - Substituted pyrrole - Heteroaromatic compound - Pyrrole - Tertiary alcohol - Tertiary aliphatic amine - 1,2-aminoalcohol - Tertiary amine - Oxacycle - Ether - Organoheterocyclic compound - Azacycle - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Alcohol - Organic nitrogen compound - Amine - Hydrocarbon derivative - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as morphinans. These are polycyclic compounds with a four-ring skeleton with three condensed six-member rings forming a partially hydrogenated phenanthrene moiety, one of which is aromatic while the two others are alicyclic.
External Descriptors
Not available