S. Yeo

Arylalkylidene rhodanine with bulky and hydrophobic functional group as selective HCV NS3 protease inhibitor.

M. Sim, W. T. Sing, C. L. Lee, 2001, Bioorganic & medicinal chemistry letters.

Characterization and molecular docking study of cathepsin L inhibitory peptides (SnuCalCpIs) from Calotropis procera R. Br

Chang Woo Kwon, P. Chang, S. Yeo, 2022, Scientific Reports.

Isolation of a novel protein tyrosine phosphatase inhibitor, 2-methyl-fervenulone, and its precursors from Streptomyces.

K. Lim, Y. Tan, M. Sim, 2000, Journal of natural products.

Molecular cloning and anti-invasive activity of cathepsin L propeptide-like protein from Calotropis procera R. Br. against cancer cells

A. Jeong, S. Ye, Chang Woo Kwon, 2018, Journal of enzyme inhibition and medicinal chemistry.

Biological evaluation of hepatitis C virus helicase inhibitors.

M. Sim, P. Y. Ng, S. Yeo, 2001, Bioorganic & medicinal chemistry letters.

Solid-phase synthesis of potential protein tyrosine phosphatase inhibitors via the Ugi four-component condensation.

A. Ganesan, C. Pallen, S. Yeo, 1998, Bioorganic & medicinal chemistry letters.

Isolation of streptonigrin and its novel derivative from Micromonospora as inducing agents of p53-dependent cell apoptosis.

M. Sim, Haishan Wang, J. Xu, 2002, Journal of natural products.