Search Results - "Nickerson, David F."
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Monitoring the quality of conduct of clinical trials: a survey of current practices
Published in Clinical trials (London, England) (01-06-2011)“…Background There is a little empirical evidence to determine which, if any, monitoring practices best achieve the goals of trial monitoring set forth in ICH E6…”
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Pyrazolinone-piperidine dipeptide growth hormone secretagogues (GHSs): Discovery of capromorelin
Published in Bioorganic & medicinal chemistry (20-02-2003)“…Novel pyrazolinone-piperidine dipeptide derivatives were synthesized and evaluated as growth hormone secretagogues (GHSs). Two analogues, capromorelin ( 5,…”
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Discovery and biological characterization of capromorelin analogues with extended half-lives
Published in Bioorganic & medicinal chemistry letters (18-11-2002)“…New tert-butyl, picolyl and fluorinated analogues of capromorelin ( 3), a short-acting growth hormone secretagogue (GHS), were prepared as part of a program to…”
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Theoretical study of cis-trans isomerization in simple transition-metal complexes
Published in Inorganic chemistry (01-03-1985)Get full text
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Pyrazolinone-piperidine dipeptide growth hormone secretagogues (GHSs)
Published in Bioorganic & medicinal chemistry (01-02-2003)Get full text
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Binding of fluvastatin to blood cells and plasma proteins
Published in Journal of pharmaceutical sciences (01-09-1993)“…The binding of fluvastatin, an inhibitor of hydroxymethylglutaryl coenzyme A reductase, to plasma proteins and red blood cells of rat, dog, and human in vitro…”
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First-pass metabolism and biliary recirculation of droloxifene in the female Sprague- Dawley rat
Published in Xenobiotica (01-03-1997)“…1. Utilizing a validated ultrasensitive hplc assay (lower limit of quantitation 25 pg/ml), we characterized the disposition profile of droloxifene in the…”
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The effect of oral dose volume on the absorption of a highly and a poorly water-soluble drug in the rat
Published in Biopharmaceutics & drug disposition (01-07-1994)“…The influence of dose volume on drug absorption following oral administration of a highly and a poorly water soluble drug was examined in male Sprague-Dawley…”
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