Compound Identification
SMILES
[H]C12OC3=C(OCC4([H])N=CC(C)(C)C(=O)C4(C)C)C=CC4=C3[C@@]11CCN(C)[C@]([H])(C4)[C@]1([H])C=CC2([H])O
InChIKey
InChIKey=GWOLALFQJJPZJZ-QEUPZMOISA-N
Formula
C27H34N2O4
Mass
450.579
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 Coumarans Tetrahydropyridines Alkyl aryl ethers Aralkylamines Piperidines Trialkylamines Secondary alcohols Cyclic ketones Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Azacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives Imines
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Morphinan - Phenanthrene - Tetralin - Coumaran - Alkyl aryl ether - Tetrahydropyridine - Aralkylamine - Hydropyridine - Piperidine - Benzenoid - Cyclic ketone - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - Ketone - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Oxacycle - Azacycle - Organoheterocyclic compound - Ether - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organic oxygen compound - Imine - Organic oxide - Hydrocarbon derivative - Carbonyl group - Alcohol - Amine - 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