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pubmed-article:1920351pubmed:abstractTextSeven analogues of 3-quinuclidinyl benzilate (QNB) in which one phenyl ring was replaced by an alkoxyalkyl moiety were synthesized and their affinities for the muscarinic cholinergic receptor determined. An oxygen in the beta-position of the moiety was not well-tolerated. By contrast, an oxygen in the gamma-position did not change the affinity for the muscarinic receptor. However, when a bromine was placed on the remaining phenyl ring, the affinity was significantly reduced in striking contrast to results obtained on halogenation of QNB.lld:pubmed
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pubmed-article:1920351pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:1920351pubmed:articleTitleSynthesis and muscarinic cholinergic receptor affinities of 3-quinuclidinyl alpha-(alkoxyalkyl)-alpha-aryl-alpha-hydroxyacetates.lld:pubmed
pubmed-article:1920351pubmed:affiliationSection of Radiopharmaceutical Chemistry, George Washington University Medical Center, Washington, D.C. 20037.lld:pubmed
pubmed-article:1920351pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:1920351pubmed:publicationTypeComparative Studylld:pubmed
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