Compound Identification
SMILES
CN1CC[C@]23[C@H]4OC5=C(O)C=CC(C[C@H]1[C@]2(O)CC1=C4N(CC2=CC=CC=C2)C=C1C1=CC=CC=C1)=C35
InChIKey
InChIKey=MEJFDGHXWAVSFS-NKIORRDJSA-N
Formula
C32H30N2O3
Mass
490.603
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 Phenylpyrroles Tetralins Indoles and derivatives Coumarans 1-hydroxy-2-unsubstituted benzenoids Alkyl aryl ethers Aralkylamines 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 - 3-phenylpyrrole - Tetralin - Indole or derivatives - Coumaran - Alkyl aryl ether - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Aralkylamine - Monocyclic benzene moiety - Piperidine - Substituted pyrrole - Benzenoid - Tertiary alcohol - Pyrrole - Heteroaromatic compound - Tertiary aliphatic amine - Tertiary amine - 1,2-aminoalcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Ether - Amine - Organic oxygen compound - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Alcohol - Organic nitrogen compound - 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