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Synthesis and structure-activity relationship of 3-O-acylated (-)-epigallocatechins as 5α-reductase inhibitors.
Lin SF, Lin YH, Lin M, Kao YF, Wang RW, Teng LW, Chuang SH, Chang JM, Yuan TT, Fu KC, Huang KP, Lee YS, Chiang CC, Yang SC, Lai CL, Liao CB, Chen P, Lin YS, Lai KT, Huang HJ, Yang JY, Liu CW, Wei WY, Chen CK, Hiipakka RA, Liao S, Huang JJ. Lin SF, et al. Among authors: liao cb. Eur J Med Chem. 2010 Dec;45(12):6068-76. doi: 10.1016/j.ejmech.2010.10.011. Epub 2010 Oct 15. Eur J Med Chem. 2010. PMID: 21044810
Synthesis of selenophene derivatives as novel CHK1 inhibitors.
Hong PC, Chen LJ, Lai TY, Yang HY, Chiang SJ, Lu YY, Tsai PK, Hsu HY, Wei WY, Liao CB. Hong PC, et al. Among authors: liao cb. Bioorg Med Chem Lett. 2010 Sep 1;20(17):5065-8. doi: 10.1016/j.bmcl.2010.07.034. Epub 2010 Jul 13. Bioorg Med Chem Lett. 2010. PMID: 20674356
Design and synthesis of 4-anilinoquinazolines as Raf kinase inhibitors. Part 1. Selective B-Raf/B-RafV600E and potent EGFR/VEGFR2 inhibitory 4-(3-hydroxyanilino)-6-(1H-1,2,3-triazol-4-yl)quinazolines.
Lee CI, Liao CB, Chen CS, Cheng FY, Chung YH, Wang YC, Ciou SY, Hsueh WY, Lo TH, Huang GR, Huang HY, Tsai CS, Lu YJ, Chuang SH, Huang JJ. Lee CI, et al. Among authors: liao cb. Bioorg Chem. 2021 Apr;109:104715. doi: 10.1016/j.bioorg.2021.104715. Epub 2021 Feb 8. Bioorg Chem. 2021. PMID: 33647741
11 results