Abstract
The dimerization and trimerization of the Dmt-Tic, Dmt-Aia and Dmt-Aba pharmacophores provided multiple ligands which were evaluated in vitro for opioid receptor binding and functional activity. Whereas the Tic- and Aba multimers proved to be dual and balanced delta/mu antagonists, as determined by the functional [S(35)]GTPgammaS binding assay, the dimerization of potent Aia-based 'parent' ligands unexpectedly resulted in substantial less efficient receptor binding and non-active dimeric compounds.
Copyright 2010 Elsevier Ltd. All rights reserved.
Publication types
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Research Support, N.I.H., Intramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Benzazepines / chemical synthesis
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Benzazepines / chemistry*
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Benzazepines / pharmacology
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Dimerization
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Drug Design
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Indoles / chemical synthesis
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Indoles / chemistry*
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Indoles / pharmacology
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Ligands*
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Protein Binding
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Rats
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Receptors, Opioid, delta / antagonists & inhibitors*
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Receptors, Opioid, delta / metabolism
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Receptors, Opioid, mu / antagonists & inhibitors*
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Receptors, Opioid, mu / metabolism
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Tetrahydroisoquinolines / chemical synthesis
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Tetrahydroisoquinolines / chemistry*
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Tetrahydroisoquinolines / pharmacology
Substances
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Benzazepines
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Indoles
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Ligands
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Receptors, Opioid, delta
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Receptors, Opioid, mu
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Tetrahydroisoquinolines