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- W1995810318 abstract "Several 6-chloro-2,3-disubstituted imidazo[l,2-b]pyndazines, selected from a number of synthetic imidazo[l,2-b]pyridazines which lacked significant binding activity at central benzodiazepine receptors, potently inhibit [3H]diazepam, [3H]Ro5-4864 and [3H]PK11 195 binding to rat kidney mitochondnal membranes. In membrane preparations from cultures of THP-1 cells, a human monocytic leukaemia cell line, the isoqumoline carboxamide PK11195 is strongly bound but the benzodiazepine ligands, diazepam and Ro5-4864, are much more weakly bound. The imidazopyridazine compounds which bind strongly to mitochondrial benzodiazepine receptors are very potent displacers of [3H]PK 11195 bound to the THP-1 membranes. It appears that the binding properties of these new imidazopyridazine ligands at ‘peripheral-type’ benzodiazepine receptors resemble those of the isoquinoline carboxamides more than those of the benzodiazepines." @default.
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- W1995810318 date "1995-11-01" @default.
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- W1995810318 title "New imidazo[1,2-b]pyridazine ligands for peripheral-type benzodiazepine receptors on mitochondria and monocytes" @default.
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- W1995810318 doi "https://doi.org/10.1016/0024-3205(95)02233-9" @default.
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