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
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:
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