Novel nanomolar imidazo[4,5-b]pyridines as selective nitric oxide synthase (iNOS) inhibitors: SAR and structural insights von Grädler, Ulrich, Fuchß, Thomas, Ulrich, Wolf-Rüdiger, Boer, Rainer, Strub, Andreas, Hesslinger, Christian, Anézo, Céline, Diederichs, Kay, Zaliani, Andrea

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The Inhibitory Potency and Selectivity of Arginine Substrate Site Nitric-Oxide Synthase Inhibitors Is Solely Determined by Their Affinity toward the Different Isoenzymes von Boer, R, Ulrich, W R, Klein, T, Mirau, B, Haas, S, Baur, I

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Structure and potential C‐terminal dimerization of a recombinant mutant of surfactant‐associated protein C in chloroform/methanol von Luy, Burkhard, Diener, Alexander, Hummel, Rolf‐Peter, Sturm, Ernst, Ulrich, Wolf‐Rüdiger, Griesinger, Christian

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Characterization of the Dexniguldipine Binding Site in the Multidrug Resistance-Related Transport Protein P-Glycoprotein by Photoaffinity Labeling and Mass Spectrometry von Borchers, Christoph, Boer, Rainer, Klemm, Kurt, Figala, Volker, Denzinger, Thomas, Ulrich, Wolf-Rüdiger, Haas, Sabine, Ise, Wolfgang, Gekeler, Volker, Przybylski, Michael

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The Novel Imidazopyridine 2-[2-(4-Methoxy-pyridin-2-yl)-ethyl]-3H-imidazo[4,5-b]pyridine (BYK191023) Is a Highly Selective Inhibitor of the Inducible Nitric-Oxide Synthase von Strub, Andreas, Ulrich, Wolf-Rüdiger, Hesslinger, Christian, Eltze, Manfrid, Fuchss, Thomas, Strassner, Jochen, Strand, Susanne, Lehner, Martin D, Boer, Rainer

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Stereoselective inhibition of thromboxane-induced coronary vasoconstriction by 1,4-dihydropyridine calcium channel antagonists von Eltze, Manfrid, Sanders, Karl H., Boss, Hildegard, Boer, Rainer, Ulrich, Wolf-Rüdiger, Flockerzi, Dieter

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Rhodamine 123 efflux modulation in the presence of low or high serum from CD56 + hematopoietic cells or CD34 + leukemic blasts by B9309-068, a newly designed pyridine derivative von Beck, James Friedrich, Buchholz, Frank, Ulrich, Wolf-Rüdiger, Boer, Rainer, Sanders, Karl Heinrich, Niethammer, Dietrich, Gekeler, Volker

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Interaction of cytostatics and chemosensitizers with the dexniguldipine binding site on P-glycoprotein von Boer, Rainer, Ulrich, Wolf-Rüdiger, Haas, Sabine, Borchers, Christoph, Gekeler, Volker, Boss, Hildegard, Przybylski, Michael, Schödl, Angelika

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The leukotriene LTD4 receptor antagonist MK571 specifically modulates MRP associated multidrug resistance von Gekeler, V, Ise, W, Sanders, K H, Ulrich, W R, Beck, J

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Cope Rearrangement with Dipolar Intermediates von Gompper, Rudolf, Ulrich, Wolf-Rüdiger

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Hetero Cope Rearrangements with Dipolar Intermediates von Gompper, Rudolf, Ulrich, Wolf-Rüdiger

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The Novel Imidazopyridine 2-[2-(4-Methoxy-pyridin-2-yl)-ethyl]-3 H -imidazo[4,5- b ]pyridine (BYK191023) Is a Highly Selective Inhibitor of the Inducible Nitric-Oxide Synthase von Strub, Andreas, Ulrich, Wolf-Rüdiger, Hesslinger, Christian, Eltze, Manfrid, Fuchß, Thomas, Strassner, Jochen, Strand, Susanne, Lehner, Martin D., Boer, Rainer

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O34. Potent and highly selective inhibition of the inducible nitric oxide synthase in vitro and in vivo by the novel imidazopyridine BYK191023 von Strub, Andreas, Hesslinger, Christian, Lehner, Martin D., Ulrich, Wolf-Rüdiger, Eltze, Manfrid, Fuchß, Thomas, Boer, Rainer

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In vitro and in vivo uroselectivity of B8805-033, an antagonist with high affinity at prostatic α 1A - vs. α 1B - and α 1D -adrenoceptors von Eltze, Manfrid, Boer, Rainer, Michel, Martin, Hein, Peter, Testa, Rodolfo, Ulrich, Wolf-Rüdiger, Kolassa, Norbert, Sanders, Karl

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B9209-005, an azido derivative of the chemosensitizer dexniguldipine-HCl, photolabels P-glycoprotein von Borchers, C, Ulrich, W R, Klemm, K, Ise, W, Gekeler, V, Haas, S, Schödl, A, Conrad, J, Przybylski, M, Boer, R

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Alkoxypyridine-derivatives von Ulrich, Wolf-Rüdiger

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Diazocine derivatives and their use as tryptase inhibitors von Ulrich, Wolf-Rüdiger

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Tryptase inhibitors von Ulrich, Wolf-Rüdiger

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Surfactant protein C esters von Ulrich, Wolf-Rüdiger, Sturm, Ernst

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Surfactant protein C esters von Ulrich, Wolf-Rüdiger, Sturm, Ernst

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