Structure Information
Structure

Compound Identification

SMILES

OC1=C2O[C@H]3C4=C(C[C@@]5(O)C6CC(C=C1)=C2[C@@]35CCN6CC1CC1)C1=CC=CC=C1N4CC1=CC(NC(=O)CBr)=CC=C1

InChIKey

InChIKey=HDUSMYFDADSZOJ-MYHPFTMJSA-N

Formula

C35H34BrN3O4

Mass

640.578

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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 - Carbazole - Tetralin - 3-alkylindole - N-alkylindole - Anilide - Coumaran - Indole or derivatives - Indole - N-arylamide - Aralkylamine - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Alkyl aryl ether - Monocyclic benzene moiety - Benzenoid - Substituted pyrrole - Piperidine - Pyrrole - Tertiary alcohol - Heteroaromatic compound - 1,2-aminoalcohol - Amino acid or derivatives - Carboxamide group - Tertiary aliphatic amine - Tertiary amine - Secondary carboxylic acid amide - Organoheterocyclic compound - Carboxylic acid derivative - Azacycle - Oxacycle - Ether - Amine - Hydrocarbon derivative - Organohalogen compound - Organic nitrogen compound - Carbonyl group - Organic oxide - Organic oxygen compound - Alcohol - Organonitrogen compound - Organooxygen compound - Organobromide - Alkyl bromide - Alkyl halide - 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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