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I-Lin Lu

National Defense Medical Center

11

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504

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Structure-based inhibitors exhibit differential activities against Helicobacter pylori and Escherichia coli undecaprenyl pyrophosphate synthases.

2008 BioMed Research International
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2-[3-[2-[(2S)-2-cyano-1-pyrrolidinyl]-2-oxoethylamino]-3-methyl-1-oxobutyl]-1,2,3,4-tetrahydroisoquinoline : A potent, selective, and orally bioavailable dipeptide-derived inhibitor of dipeptidyl peptidase IV

2006 Journal of Medicinal Chemistry
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Discovery of a Novel Family of SARS-CoV Protease Inhibitors by Virtual Screening and 3D-QSAR Studies

2006 Journal of Medicinal Chemistry
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Structural basis for the structure-activity relationships of peroxisome proliferator-activated receptor agonists

2006 Journal of Medicinal Chemistry
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Indol-1-yl Acetic Acids as Peroxisome Proliferator-Activated Receptor Agonists: Design, Synthesis, Structural Biology, and Molecular Docking Studies

2006 Journal of Medicinal Chemistry
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Structure-Based Drug Design of a Novel Family of PPARgamma Partial Agonists: Virtual Screening, X-ray Crystallography, and in Vitro/in Vivo Biological Activities

2006 Journal of Medicinal Chemistry
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Structure-Based Drug Design and Structural Biology Study of Novel Nonpeptide Inhibitors of Severe Acute Respiratory Syndrome Coronavirus Main Protease

2006 Journal of Medicinal Chemistry
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Novel indole-based peroxisome proliferator-activated receptor agonists: design, SAR, structural biology, and biological activities.

2005 Journal of Medicinal Chemistry
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Glutamic acid analogues as potent dipeptidyl peptidase IV and 8 inhibitors

2005 Bioorganic & Medicinal Chemistry Letters
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Citations (31)