Structure-based design of the first potent and selective inhibitor of human non-pancreatic secretory phospholipase A2 von Schevitz, R W, Bach, N J, Carlson, D G, Chirgadze, N Y, Clawson, D K, Dillard, R D, Draheim, S E, Hartley, L W, Jones, N D, Mihelich, E D

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The crystal structures of human α-thrombin complexed with active site-directed diamino benzo[b]thiophene derivatives: A binding mode for a structurally novel class of inhibitors von CHIRGADZE, N.Y., SALL, D.J., BRIGGS, S.L., CLAWSON, D.K., ZHANG, M., SMITH, G.F., SCHEVITZ, R.W.

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Crystals of the trp repressor-operator complex suitable for X-ray diffraction analysis von Joachimiak, A., Marmorstein, R.Q., Schevitz, R.W., Mandecki, W., Fox, J.L., Sigler, P.B.

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HIDRAZIDI 1-H-INDOL-3-SIRĆETNE KISLEINE KAO INHIBITORI SPLA2 von DILLARD, R.D, HERMANN, R.B, DRAHEIM, S.E, SCHEVITZ, R.W, BACH, N.J

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1H-INDOL-3-ACETAMIDI KAO INHIBITORI s PLA2 von DILLARD, R.D, DRAHEIM, S.E, SCHEVITZ, R.W, HER-MANN, R.B, BACH, N.J

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Structure-based design of the first potent and selective inhibitor of human non-pancreatic secretory phospholipase A 2 von Schevitz, R.W, Bach, N.J, Carlson, D.G, Chirgadze, N.Y, Clawson, D.K, Dillard, R.D, Draheim, S.E, Hartley, L.W, Jones, N.D, Mihelich, E.D, Olkowski, J.L, Snyder, D.W, Sommers, C, Wery, J.-P

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