Search Results - "Trummlitz, Gunter"

Structure and physicochemical properties of meloxicam, a new NSAID by Luger, Peter, Daneck, Klaus, Engel, Wolfhard, Trummlitz, Günter, Wagner, Klaus

“…The physicochemical properties of meloxicam, a new NSAID, were investigated. Dependent on pH and solvents used, X-ray crystallography showed that meloxicam…”
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C-Glycosyl nucleosides. VIII. Synthesis of 3-methylshowdomycin by Trummlitz, Gunter, Repke, David B, Moffatt, John G

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COX-2 selectivity and inflammatory processes by van Ryn, J, Trummlitz, G, Pairet, M

“…Increasing amounts of experimental and clinical data support the role of selective cyclooxygenase (COX)-2 inhibition in anti-inflammatory processes and the…”
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Synthesis of a biologically active gougerotin analog by Lichtenthaler, F W, Trummlitz, G, Bambach, G, Rychlik, I

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C-Glycosyl nucleosides. III. Facile synthesis of the nucleoside antibiotic showdomycin by Trummlitz, G, Moffatt, J. G

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Tricyclic compounds as selective muscarinic receptor antagonists. 3. Structure-selectivity relationships in a series of cardioselective (M2) antimuscarinics by Engel, Wolfhard W, Eberlein, Wolfgang G, Mihm, Gerhard, Hammer, Rudolf, Trummlitz, Guenter

“…On the basis of the cardioselective muscarinic receptor antagonist AF-DX 116 (2), a series of 11-substituted pyridobenzodiazepinones (9-35) was prepared and…”
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Tricyclic compounds as selective antimuscarinics. 1. Structural requirements for selectivity toward the muscarinic acetylcholine receptor in a series of pirenzepine and imipramine analogues by Eberlein, W G, Trummlitz, G, Engel, W W, Schmidt, G, Pelzer, H, Mayer, N

“…The M1-selective antiulcer drug pirenzepine (1) is a tricyclic compound with close resemblance to tricyclic psychotropic agents such as imipramine (2). Despite…”
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Tricyclic compounds as selective antimuscarinics. 2. Structure-activity relationships of M1-selective antimuscarinics related to pirenzepine by Eberlein, Wolfgang G, Engel, Wolfhard W, Trummlitz, Guenter, Schmidt, Guenther, Hammer, Rudolf

“…In order to gain some insight into those structural features that control M1 selectivity, a selected set of pirenzepine analogues has been studied in which…”
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