Structure Information
Structure

Compound Identification

SMILES

[O-]C(=O)CC1=CC=CC=C1NC1=C(Cl)C=CC=C1Cl.COC1=C2O[C@H]3[C@@H](O)C=C[C@H]4[C@H]5CC(C=C1)=C2[C@@]34CC[NH+]5C

InChIKey

InChIKey=MUACAZBFPOZUHP-FFHNEAJVSA-N

Formula

C32H32Cl2N2O5

Mass

595.52

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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

Not available

Substituents

Morphinan - Phenanthrene - Tetralin - Coumaran - Anisole - 1,3-dichlorobenzene - Aniline or substituted anilines - Phenol ether - Alkyl aryl ether - Chlorobenzene - Halobenzene - Aralkylamine - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Piperidine - Primary aromatic amine - Benzenoid - Quaternary ammonium salt - Tertiary aliphatic amine - Amino acid or derivatives - Tertiary amine - Secondary alcohol - Carboxylic acid salt - Amino acid - Organoheterocyclic compound - Azacycle - Secondary amine - Carboxylic acid derivative - Oxacycle - Monocarboxylic acid or derivatives - Ether - Carboxylic acid - Organic zwitterion - Organic oxide - Hydrocarbon derivative - Organohalogen compound - Carbonyl group - Amine - Organic nitrogen compound - Alcohol - Organochloride - Organonitrogen compound - Organooxygen compound - Organic oxygen 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

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