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Results: 1-7 |
Results: 7

Authors: Neumann, U Schechter, NM Gutschow, M
Citation: U. Neumann et al., Inhibition of human chymase by 2-amino-3,1-benzoxazin-4-ones, BIO MED CH, 9(4), 2001, pp. 947-954

Authors: Carr, MJ Schechter, NM Undem, BJ
Citation: Mj. Carr et al., Trypsin-induced, neurokinin-mediated contraction of guinea pig bronchus, AM J R CRIT, 162(5), 2000, pp. 1662-1667

Authors: Groutas, WC Schechter, NM He, S Yu, HY Huang, P Tu, J
Citation: Wc. Groutas et al., Human chymase inhibitors based on the 1,2,5-thiadiazolidin-3-one 1,1 dioxide scaffold, BIOORG MED, 9(15), 1999, pp. 2199-2204

Authors: Pereira, PJB Wang, ZM Rubin, H Huber, R Bode, W Schechter, NM Strobl, S
Citation: Pjb. Pereira et al., The 2.2 a crystal structure of human chymase in complex with succinyl-Ala-Ala-Pro-Phe-chloromethylketone: Structural explanation for its dipeptidyl carboxypeptidase specificity (vol 286, pg 163, 1998), J MOL BIOL, 287(4), 1999, pp. 817-817

Authors: Huber, R Bode, W Schechter, NM Strobl, S
Citation: R. Huber et al., The 2.2 angstrom crystal structure of human chymase in complex with succinyl-Ala-Ala-Pro-Phe-chloromethylketone: Structural explanation for its dipeptidyl carboxypeptidase specificity, J MOL BIOL, 286(1), 1999, pp. 163-173

Authors: Walter, M Sutton, RM Schechter, NM
Citation: M. Walter et al., Highly efficient inhibition of human chymase by alpha(2)-macroglobulin, ARCH BIOCH, 368(2), 1999, pp. 276-284

Authors: Kuang, RZ Epp, JB Ruan, SM Yu, HY Huang, P He, S Tu, J Schechter, NM Turbov, J Froelich, CJ Groutas, WC
Citation: Rz. Kuang et al., A general inhibitor scaffold for serine proteases with a (chymo)trypsin-like fold: Solution-phase construction and evaluation of the first series of libraries of mechanism-based inhibitors, J AM CHEM S, 121(35), 1999, pp. 8128-8129
Risultati: 1-7 |