Structure Information
Structure

Compound Identification

SMILES

OC1=C2O[C@H]3C4=C(C[C@@]5(O)[C@H]6CC(C=C1)=C2[C@@]35CCN6CC1CC1)C=C(C=N4)C1=CC=C(C=C1)[N+]([O-])=O

InChIKey

InChIKey=TWQBUMRBIFNGEP-FQYQUSJJSA-N

Formula

C29H27N3O5

Mass

497.551

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Alkaloids and derivatives

Class

Morphinans

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Morphinans

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Morphinan - Phenylquinoline - Phenanthrene - 3-phenylpyridine - Tetralin - Quinoline - Coumaran - Nitrobenzene - Nitroaromatic compound - Alkyl aryl ether - 1-hydroxy-2-unsubstituted benzenoid - Aralkylamine - Phenol - Piperidine - Pyridine - Monocyclic benzene moiety - Benzenoid - Tertiary alcohol - Heteroaromatic compound - 1,2-aminoalcohol - C-nitro compound - Organic nitro compound - Tertiary amine - Tertiary aliphatic amine - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Ether - Organic oxoazanium - Oxacycle - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Hydrocarbon derivative - Alcohol - Organonitrogen compound - Organooxygen compound - Organic zwitterion - Organic oxygen compound - Organic nitrogen compound - Amine - Organic salt - Organic oxide - 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

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