| Issue Date | Title | Author(s) | Relation | scopus | WOS | Fulltext/Archive link |
| 2006 | Aminopeptidase p mediated detoxification of organophosphonate analogues of sarin: mechanistic and stereochemical study at the phosphorus atom of the substrate. | Huang, LF; Su, B; Jao, SC; Liu, KT; Li, WS | Chembiochem : a European journal of chemical biology 7(3), 506-14 | | | |
| 2006 | Design of potent inhibitors for <i>Schistosoma japonica</i> glutathione S-transferase. | Jao, SC; Chen, J; Yang, K; Li, WS | Bioorganic & Medicinal Chemistry 14, 304-318 | | | |
| 2006 | Design of potent inhibitors for Schistosoma japonica glutathione S-transferase. | Jao, SC; Chen, J; Yang, K; Li, WS | Bioorganic & medicinal chemistry 14(2), 304-18 | | | |
| 2007 | Enzymatic and Nonenzymatic Synthesis of Glutathione Conjugates: Application to the Understanding of Parasite's Defense System and Alternative to the Discovery of Potent Glutathione S-Transferase Inhibitors. | Lo, WJ; Chiou, YC; Hsu, YT; Lam, WS; Chang, MY; Jao, SC; Li, WS | Bioconjugate Chemistry 18, 109-120 | | | |
| 2008 | Evaluation of organophosphorus chemicals-degrading enzymes: a comparison of Escherichia coli and human cytosolic aminopeptidase P. | Hsu, YT; Su, CY; Du, HC; Jao, SC; Li, WS | Chemistry & biodiversity 5(7), 1401-11 | | | |
| 2011 | Inhibition of Glutathione S-Transferase M1 by New Gabosine Analogues Is Essential for Overcoming Cisplatin Resistance in Lung Cancer Cells. | Wang, CH; Wu, HT; Cheng, HM; Yen, TJ; Lu, IH; Chang, HC; Jao, SC; Shing, TK; Li, WS | Journal of medicinal chemistry 54(24), 8574-81 | | | |
| 2017 | Modulation of β-galactoside α2,6-sialyltranferase 1 in a fructose-responsive manner promotes pancreatic cancer metastasis | Hsieh, CC; Shyr, YM; Liao, WY; Chen, TH; Wang, SE; Lu, PC; Lin, PY; Hsiao, M; Li, WS; Sher, YP; Shen, CN | Oncotarget 8(5):, 7691-7709 | | | |
| 2016 | Nature-inspired design of tetraindoles: Optimization of the core structure and evaluation of structure-activity relationship. | Abdu-Allah, HH; Huang, ST; Chang, TT; Chen, CL; Wu, HC; Li, WS | Bioorganic & medicinal chemistry letters 26(18), 4497-4503 | | | |
| 2010 | Overcoming the drug resistance in breast cancer cells by rational design of efficient glutathione S-transferase inhibitors. | Li, WS; Lam, WS; Liu, KC; Wang, CH; Chang, HC; Jen, YC; Hsu, YT; Shivatare, SS; Jao, SC | Organic letters 12(1), 20-3 | | | |
| 2011 | Polyfluorinated bipyridine cisplatins manipulate cytotoxicity through the induction of S-G(2)/M arrest and partial intercalation mechanism. | Chang, TT; More, SV; Lu, N; Jhuo, JW; Chen, YC; Jao, SC; Li, WS | Bioorganic & medicinal chemistry 19(16), 4887-94 | | | |
| 2010 | Synthesis and structure-activity relationships of novel furazan-3,4-diamide analogs as potent anti-cancer agents. | Li, WS; More, SV; Wang, CH; Jen, YC; Yao, CF; Wang, TF; Hung, CC; Jao, SC | Bioorganic & medicinal chemistry letters 20(3), 1148-52 | | | |
| 2016 | Synthesis of B- and C-ring-modified lithocholic acid analogues as potential sialyltransferase inhibitors. | Abdu-Allah, HH; Chang, TT; Li, WS | Steroids 112, 54-61 | | | |
| 2014 | The tetraindole SK228 reverses the epithelial-to-mesenchymal transition of breast cancer cells by up-regulating members of the miR-200 family. | Wang, CH; Chen, CL; More, SV; Hsiao, PW; Hung, WC; Li, WS | PLoS ONE 9(6), e101088 | | | |
| 2006 | Tyrosine 387 and arginine 404 are critical in the hydrolytic mechanism of Escherichia coli aminopeptidase P. | Jao, SC; Huang, LF; Hwang, SM; Li, WS | Biochemistry 45(6), 1547-53 | | | |
