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.
journal_name
Life Scijournal_title
Life sciencesauthors
Römer D,Büscher HH,Hill RC,Maurer R,Petcher TJ,Zeugner H,Benson W,Finner E,Milkowski W,Thies PWdoi
10.1016/0024-3205(82)90346-0subject
Has Abstractpub_date
1982-09-20 00:00:00pages
1217-20issue
12-13eissn
0024-3205issn
1879-0631pii
0024-3205(82)90346-0journal_volume
31pub_type
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