Shih‐Hung Lin

<scp>S</scp>creening alpha‐glucosidase and alpha‐amylase inhibitors from natural compounds by molecular docking <i>in silico</i>

Chien‐Hung Jhong, Jirawat Riyaphan, Shih‐Hung Lin et al. · BioFactors · 2015 · 164 citations

Nutraceutical Ingredient, Natural Compounds, Enzymatic Modification +16

A novel inhibitor, 16-hydroxy-cleroda-3,13-dien-16,15-olide, blocks the autophosphorylation site of focal adhesion kinase (Y397) by molecular docking

Varadharajan Thiyagarajan, Shih‐Hung Lin, Yi‐Chen Chia et al. · Biochimica et Biophysica Acta (BBA) - General Subjects · 2013 · 46 citations

Novel Inhibitor, Signal Transduction, Focal Adhesion Kinase +11

Peptide inhibitors of human HMG-CoA reductase as potential hypocholesterolemia agents

Shih‐Hung Lin, Ding‐Kwo Chang, Mei-Ju Chou et al. · Biochemical and Biophysical Research Communications · 2014 · 26 citations

Metabolic Syndrome, Oxysterol, Biochemistry +9

Xanthone derivatives could be potential antibiotics: virtual screening for the inhibitors of enzyme I of bacterial phosphoenolpyruvate-dependent phosphotransferase system

Kuo-Jien Huang, Shih‐Hung Lin, Meei‐Ru Lin et al. · The Journal of Antibiotics · 2013 · 20 citations · Full text

Virtual Screening, Antibiotics, Biochemistry +10

Syntheses of some α-cyclic tripeptides as potential inhibitors for HMG-CoA Reductase

Subrata Chakraborty, Shih‐Hung Lin, David Shiuan et al. · Amino Acids · 2015 · 13 citations

Medicinal Chemistry, Biosynthesis, Biochemistry +10