Ting-Chien Lin

Entropy-driven binding of gut bacterial β-glucuronidase inhibitors ameliorates irinotecan-induced toxicity

S. Roffler, Chun-Hung Lin, Lun-Fu Yeh, 2021, Communications biology.

Chemoenzymatic Synthesis of GDP‐L‐Fucose Derivatives as Potent and Selective α‐1,3‐Fucosyltransferase Inhibitors

Chun-Hung Lin, H. Narimatsu, J. Gervay-Hague, 2012 .

An Acyloxymethyl Ketone‐Based Probe to Monitor the Activity of Glutathionylspermidine Amidase in Escherichia coli

Chun-Hung Lin, B. Chiang, C. Chong, 2011, Chembiochem : a European journal of chemical biology.

β-Glucuronidases of opportunistic bacteria are the major contributors to xenobiotic-induced toxicity in the gut

Chun-Hung Lin, Chia-Yi Hsu, T. Hsieh, 2018, Scientific Reports.

A New Method of Preparing Aurone by Marine Actinomycetes and Its Potential Application in Agricultural Fungicides

Bin Liu, Xiaomeng Li, Zhong Li, 2022, Molecules.

Polyhydroxylated pyrrolidine and 2-oxapyrrolizidine as glycosidase inhibitors

Jim-Min Fang, Chun-Hung Lin, Ting-Chien Lin, 2013 .

β-Glucuronidases of opportunistic bacteria are the major contributors to xenobiotic-induced toxicity in the gut

Chun-Hung Lin, Chia-Yi Hsu, T. Hsieh, 2018, Scientific Reports.

Dual thio-digalactoside-binding modes of human galectins as the structural basis for the design of potent and selective inhibitors

S. Hsu, Fu-Tong Liu, Chun-Hung Lin, 2016, Scientific Reports.