Search Results - "Trout, Robert E Lee"
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Systemic activation of the transient receptor potential vanilloid subtype 4 channel causes endothelial failure and circulatory collapse: Part 2
Published in The Journal of pharmacology and experimental therapeutics (01-08-2008)“…The transient receptor potential (TRP) vanilloid subtype 4 (V4) is a nonselective cation channel that exhibits polymodal activation and is expressed in the…”
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Discovery of Taniborbactam (VNRX-5133): A Broad-Spectrum Serine- and Metallo-β-lactamase Inhibitor for Carbapenem-Resistant Bacterial Infections
Published in Journal of medicinal chemistry (26-03-2020)“…A major resistance mechanism in Gram-negative bacteria is the production of β-lactamase enzymes. Originally recognized for their ability to hydrolyze…”
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Spongipyran synthetic studies. Total synthesis of (+)-spongistatin 2
Published in Tetrahedron (15-08-2009)“…Evolution of a convergent synthetic strategy to access (+)-spongistatin 2 ( 2), a potent cytotoxic marine macrolide, is described. Highlights of the synthesis…”
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Antagonists of the Calcium Receptor I. Amino Alcohol-Based Parathyroid Hormone Secretagogues
Published in Journal of medicinal chemistry (09-07-2009)“…Functional screening of the former SmithKline Beecham compound collection against the human calcium receptor (CaR) resulted in the identification of the amino…”
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Azepanone-Based Inhibitors of Human Cathepsin L
Published in Journal of medicinal chemistry (03-11-2005)“…The extension of a previously reported cathepsin K azepanone-based inhibitor template to the design and synthesis of potent and selective inhibitors of the…”
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Spongistatin synthetic studies. 2. Assembly of the C(18–28) spiroketal
Published in Tetrahedron letters (15-12-1997)“…The C(18–28) CD-ring spiroketal subunit of the spongistatins, marine polyether macrolides with unprecedented antitumor activity, has been generated via a…”
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Asymmetric synthesis of a potent azepanone-based inhibitor of the cysteine protease cathepsin K
Published in Tetrahedron letters (18-04-2005)“…[Display omitted] In this account we detail the asymmetric synthesis of 1, a potent azepanone-based inhibitor of cathepsin K ( K i = 0.16 nM), which has been…”
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Cyclic Ketone Inhibitors of the Cysteine Protease Cathepsin K
Published in Journal of medicinal chemistry (01-03-2001)“…Cathepsin K (EC 3.4.22.38), a cysteine protease of the papain superfamily, is predominantly expressed in osteoclasts and has been postulated as a target for…”
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