Abstract
Molecular modeling studies based on the potent NK-1 antagonist CP-96,345 led us to the identification of some 2-benzylidene- and 2-benzyl-3-benzylaminoquinuclidine derivatives as potential antagonists at the NK receptor subtypes. The synthesized compounds, whose Z/E isomerism has been defined by X-ray analysis, show only moderate potency on the three neurokinin receptors. The possible reasons of the low potency exhibited by the tested compounds are discussed.
MeSH terms
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Amino Acid Sequence
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Animals
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Biphenyl Compounds / chemical synthesis
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Biphenyl Compounds / chemistry
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Biphenyl Compounds / pharmacology*
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Crystallography, X-Ray
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Dose-Response Relationship, Drug
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Guinea Pigs
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Models, Molecular
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Molecular Sequence Data
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Neurokinin-1 Receptor Antagonists*
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Rats
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Receptors, Neurokinin-2 / antagonists & inhibitors
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Receptors, Neurokinin-3 / antagonists & inhibitors
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Stereoisomerism
Substances
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Biphenyl Compounds
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Neurokinin-1 Receptor Antagonists
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Receptors, Neurokinin-2
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Receptors, Neurokinin-3
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CP 96345