Volume 13 Supplement 1

18th Scientific Symposium of the Austrian Pharmacological Society (APHAR)

Open Access

Influence of the 14-alkoxy group and the substitution in position 5 in N-methyl-14-alkoxymorphinan-6-ones on in vitro and in vivopharmacological activities

  • Tanila Ben Haddou1,
  • Roberta Lattanzi2,
  • Lucia Negri2,
  • Helmut Schmidhammer1 and
  • Mariana Spetea1Email author
BMC Pharmacology and Toxicology201213(Suppl 1):A33

DOI: 10.1186/2050-6511-13-S1-A33

Published: 17 September 2012


Opioid analgesics are the cornerstone drugs for the treatment of moderate-to-severe pain. Morphine and other analgesics like fentanyl, oxycodone and oxymorphone activate the µ opioid (MOP) receptor, the main type targeted for pharmacotherapy of pain. These drugs share the same pharmacological profiles including severe adverse effects such as respiratory depression, constipation, tolerance and physical dependence. Chemical approaches towards the identification of novel MOP analgesics with reduced side effects include structural modifications of morphinan-6-ones in key positions that are important for binding, selectivity, potency and efficacy at opioid receptors. A representative example is the development of the 14-O-methyl-substituted derivative of the clinically used MOP analgesic oxymorphone, namely 14-O-methyloxymorphone, and its 5-methyl-substituted analogue, 14-methoxymetopon. The focus of the present work is on structure-activity relationship (SAR) studies and in vitro and in vivo pharmacological investigations on a series of opioid ligands differently substituted in positions 5 and 14 of the morphinan skeleton.


Radioligand binding assays were performed using rodent brain membranes. Mouse vas deferens (MVD) and guinea-pig ileum (GPI) bioassays, and [35S]GTPγS functional assays with Chinese hamster ovary (CHO) cells expressing human opioid receptors were used to assess opioid agonism. Antinociceptive properties were established using hot-plate and writhing tests in mice after subcutaneous (s.c.) administration.


Binding studies showed that all derivatives display affinities in the subnanomolar range at the MOP receptor and were MOP receptor-selective. In smooth muscle preparations and CHO cells transfected with MOP receptors they behaved as potent agonists. The differently substituted N-methylmorphinan-6-ones produced marked antinociceptive effects in mice when given s.c., being several-fold more potent than morphine. On the basis of the SAR that has emerged, certain modifications in the substitution pattern, e.g. introduction of an alkyl or arylalkyl group in position 14 and/or in position 5, result in interesting alterations in opioid activity by influencing the pharmacological properties of ligands interacting with opioid receptors. Analysis of the in vitro and in vivo opioid profile for this series of 14-alkoxymorphinans leads to an improved understanding of the relationship between affinity and/or selectivity for opioid receptors, agonist activity, antinociceptive potency and the nature of substituents in morphinans.


These results represent a useful and valuable outcome for the design and optimization of existing structural templates increasing the chance of identifying clinically useful analgesics for superior management of pain.



Supported by the Austrian Research Fund (FWF), grant TRP19-B18.

Authors’ Affiliations

Department of Pharmaceutical Chemistry, Institute of Pharmacy and Center for Molecular Biosciences, University of Innsbruck
Department of Human Physiology and Pharmacology, University ‘La Sapienza’


© Haddou et al; licensee BioMed Central Ltd. 2012

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.