First synthesis of important secondary oxidative metabolites of morphine and codeine with the Michael addition

Author:

Garadnay Sándor1,Gyulai Zsuzsanna1,Makleit Sándor1,Sipos Attila2

Affiliation:

1. 1Department of Organic Chemistry, University of Debrecen, H-4032, Debrecen, Hungary

2. 2Department of Pharmaceutical Chemistry, Medical and Health Science Center, University of Debrecen, H-4032, Debrecen, Hungary

Abstract

AbstractAbstract Morphine (1) and codeine (2) are two representatives of medically important, frequently used natural opiates, therefore the exploration of their metabolic pathways and the exact characterization of the metabolites are main targets of their pharmacological studies. These morphinans also play a crucial role in drug abuse; therefore, the analysis and preparation of the metabolites for identification and quantitation in human samples are considered important aims. In order to allow the in-depth analysis of metabolites derived from the oxidative pathways through morphinone (3) and codeinone (4), synthetic procedures have been elaborated for the gram-scale preparation of glutathione and N-acetylcysteine adducts. Primary pharmacological studies revealed the inactive nature of these metabolites in opioid receptor binding tests. Graphical abstract

Publisher

Walter de Gruyter GmbH

Subject

Materials Chemistry,General Chemistry

Reference26 articles.

1. http dx org;Girán;Tetrahedron,2008

2. http dx org;Sipos;Chemie,2009

3. http dx org;Bickley;Med Chem,2004

4. http dx org;Lee;Rev B,1988

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