Compound Identification
SMILES
NC(=S)NC1=CC2=C(NC3=C2C[C@@]2(O)[C@H]4CC5=C6C(O[C@@H]3[C@@]26CCN4CC2CC2)=C(O)C=C5)C=C1
InChIKey
InChIKey=JOWPEDUJAMNFQK-GYHUNEDQSA-N
Formula
C27H28N4O3S
Mass
488.61
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 Carbazoles 3-alkylindoles Tetralins Coumarans 1-hydroxy-2-unsubstituted benzenoids Alkyl aryl ethers Aralkylamines Piperidines Tertiary alcohols Pyrroles Heteroaromatic compounds Trialkylamines 1,2-aminoalcohols Thioureas Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Morphinan - Phenanthrene - Carbazole - Tetralin - 3-alkylindole - Indole - Indole or derivatives - Coumaran - Alkyl aryl ether - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Aralkylamine - Piperidine - Benzenoid - Tertiary alcohol - Pyrrole - Heteroaromatic compound - Tertiary aliphatic amine - Thiourea - Tertiary amine - 1,2-aminoalcohol - Oxacycle - Organoheterocyclic compound - Azacycle - Ether - Amine - Organic oxygen compound - Alcohol - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organosulfur 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