Pharmacological profiles of tonazocine (Win 42156) and zenazocine (Win 42964)

  title={Pharmacological profiles of tonazocine (Win 42156) and zenazocine (Win 42964)},
  author={S. J. Ward and Anne K. Pierson and William F. Michne},
7 Citations
Benzomorphan Skeleton as Scaffold for Analgesic , Antiviral and Antitumoral drugs
Based upon these considerations, the design, synthesis and biological evaluation of benzomorphan-based compounds as putative antiviral and/or antitumoral drug candidates could represent a valid and versatile strategy.
The Oxford Catalogue of Opioids: A systematic synthesis of opioid drug names and their pharmacology
The number of opioid drugs developed and to catalogue them based on their pharmacology will centralize and disseminate information that could assist researchers, prescribers, and the public to improve the safe use of opioids.


The effects of morphine- and nalorphine- like drugs in the nondependent and morphine-dependent chronic spinal dog.
It has been shown that buprenorphine is a partial agonist of the mu type which both suppressed and precipitated abstinence in the morphine-dependent dog while morphine and propoxyphene are stronger agonists.
The analgesic effectiveness of nalorphine and nalorphine-morphine combinations in man.
The data suggest a significant species difference in nalorphine effect in animals, and the difficulties involved in the formulation of clinically useful naloralorphine-morphine mixtures are discussed.
A new example of a morphine‐sensitive neuro‐effector junction: Adrenergic transmission in the mouse vas deferens
It is concluded that adrenergic neurotransmission in the mouse vas deferens differs in some important way from that at the more common, morphine-insensitive, adrenergic junctions.
(2,6-Methano-3-benzazocin-11 beta-yl)alkanones. 1. Alkylalkanones: a new series of N-methyl derivatives with novel opiate activity profiles.
A general stereospecific synthesis of (N-methyl-2,6-methano-3-benzazocin-11 beta-yl)alkanones is described and applied to the preparation of a series of alkyl ketones wherein the alkyl group is a
Drug antagonism and pAx.
  • H. Schild
  • Chemistry, Medicine
    Pharmacological reviews
  • 1957