Compound Identification
SMILES
[H][C@@]12OC3=C(O)C=CC4=C3C11CCN(CCC)C([H])(C4)C11C[C@]([H])([C@@](C)(O)C3=CC=CC=C3)[C@]2(OC)C=C1
InChIKey
InChIKey=WHXZIYBKAHZLOV-ZDPIIRMKSA-N
Formula
C30H35NO4
Mass
473.613
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
Benzylisoquinolines Phenanthrenes and derivatives Tetralins Azaspirodecane derivatives Coumarans 1-hydroxy-2-unsubstituted benzenoids Alkyl aryl ethers Aralkylamines Piperidines Benzene and substituted derivatives Tertiary alcohols Trialkylamines Oxacyclic compounds Azacyclic compounds Dialkyl ethers Aromatic alcohols Organopnictogen compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Benzylisoquinoline - Morphinan - Phenanthrene - Azaspirodecane - Tetralin - Coumaran - Alkyl aryl ether - 1-hydroxy-2-unsubstituted benzenoid - Aralkylamine - Monocyclic benzene moiety - Piperidine - Benzenoid - Tertiary alcohol - Tertiary aliphatic amine - Tertiary amine - Dialkyl ether - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Amine - Organic nitrogen compound - Alcohol - Hydrocarbon derivative - Organopnictogen compound - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Aromatic alcohol - 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