Structure Information
Structure

Compound Identification

SMILES

COC1=C(C=C(C=C1)C(=O)CN1CC[C@@]23CCCC[C@H]2[C@@H]1CC1=C3C=C(O)C=C1)[N+]([O-])=O

InChIKey

InChIKey=NVXSTAYMFPDPGU-OWHZGTRUSA-N

Formula

C25H28N2O5

Mass

436.508

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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 - Phenanthrene - Alkyl-phenylketone - Benzazocine - Nitrophenyl ether - Tetralin - Nitrobenzene - Methoxyaniline - Phenylketone - Anisole - Benzoyl - Phenoxy compound - Phenol ether - Nitroaromatic compound - Aryl ketone - Aryl alkyl ketone - Methoxybenzene - Aralkylamine - 1-hydroxy-2-unsubstituted benzenoid - Alkyl aryl ether - Phenol - Monocyclic benzene moiety - Benzenoid - Piperidine - Alpha-aminoketone - Organic nitro compound - Ketone - C-nitro compound - Tertiary aliphatic amine - Tertiary amine - Azacycle - Ether - Organic 1,3-dipolar compound - Organoheterocyclic compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Organic oxygen compound - Amine - Organic salt - Organonitrogen compound - Organooxygen compound - Organic zwitterion - 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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