| Literature DB >> 6292610 |
D Römer, H H Büscher, R C Hill, R Maurer, T J Petcher, H Zeugner, W Benson, E Finner, W Milkowski, P W Thies.
Abstract
Tifluadom, although structurally a 1,4 benzodiazepine, has no affinity for the 3H-flunitrazepam binding site, but is a potent displacer of 3H-bremazocine from its opioid binding site. Tifluadom is characterised as an opiate kappa-receptor agonist in vitro and in vivo with potent analgesic activity in animals and no dependence potential.Entities:
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Year: 1982 PMID: 6292610 DOI: 10.1016/0024-3205(82)90346-0
Source DB: PubMed Journal: Life Sci ISSN: 0024-3205 Impact factor: 5.037