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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
25
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pubmed:dateCreated |
1996-1-4
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pubmed:abstractText |
Several 6-chloro-2,3-disubstituted imidazo[1,2-b]pyridazines, selected from a number of synthetic imidazo[1,2-b]pyridazines which lacked significant binding activity at central benzodiazepine receptors, potently inhibit [3H]diazepam, [3H]Ro5-4864 and [3H]PK11195 binding to rat kidney mitochondrial membranes. In membrane preparations from cultures of THP-1 cells, a human monocytic leukaemia cell line, the isoquinoline 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]PK11195 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.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
0024-3205
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
57
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
PL381-6
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:7491086-Animals,
pubmed-meshheading:7491086-Cell Line,
pubmed-meshheading:7491086-Dose-Response Relationship, Drug,
pubmed-meshheading:7491086-Humans,
pubmed-meshheading:7491086-Ligands,
pubmed-meshheading:7491086-Male,
pubmed-meshheading:7491086-Mitochondria,
pubmed-meshheading:7491086-Monocytes,
pubmed-meshheading:7491086-Pyridazines,
pubmed-meshheading:7491086-Rats,
pubmed-meshheading:7491086-Rats, Wistar,
pubmed-meshheading:7491086-Receptors, GABA-A
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pubmed:year |
1995
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pubmed:articleTitle |
New imidazo[1,2-b]pyridazine ligands for peripheral-type benzodiazepine receptors on mitochondria and monocytes.
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pubmed:affiliation |
Visual Sciences Group, Research School of Biological Sciences, Australian National University, Canberra, Australia.
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pubmed:publicationType |
Journal Article
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