J. Tu

Potent inhibition of serine proteases by heterocyclic sulfide derivatives of 1,2,5-thiadiazolidin-3-one 1,1 dioxide.

W. Groutas, R. Kuang, H. Chan, 2000, Bioorganic & medicinal chemistry.

Utilization of the 1,2,5-thiadiazolidin-3-one 1,1 dioxide scaffold in the design of potent inhibitors of serine proteases: SAR studies using carboxylates.

W. Groutas, S. Ruan, R. Kuang, 2000, Bioorganic & medicinal chemistry.

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

N. Schechter, W. Groutas, S. Ruan, 1999 .

Mechanism-based inactivation of human leukocyte elastase via an enzyme-induced sulfonamide fragmentation process.

M. V. van Stipdonk, W. Groutas, K. Alliston, 2004, Archives of biochemistry and biophysics.

Inhibition of serine proteases by functionalized sulfonamides coupled to the 1,2,5-thiadiazolidin-3-one 1,1 dioxide scaffold.

W. Groutas, S. Ruan, R. Kuang, 2001, Bioorganic & medicinal chemistry.

Human chymase inhibitors based on the 1,2,5-thiadiazolidin-3-one 1,1 dioxide scaffold.

N. Schechter, W. Groutas, P. Huang, 1999, Bioorganic & medicinal chemistry letters.

Isolated single iron atoms anchored on a N, S-codoped hierarchically ordered porous carbon framework for highly efficient oxygen reduction

Xin Jia, Xinghuan Liu, Caixia Xu, 2021 .