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    Showing items 1-25 of 26. (2 Page(s) Totally)
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    DateTitleRelation
    2016-04 Discovery and development of tylophorine derived dibenzoquinolines-33b compounds into therapeutic agents The FASEB Journal. 2016 Apr;30(1, Suppl.):Meeting Abstract lb56.
    2015-04 Tylophorine compounds exert anti-cancer activity by targeting a ribonucleoprotein complex containing caprin-1 and c-Myc mRNA FASEB Journal. 2015 Apr;29(1, Suppl.):Abstract number LB132
    2014-11 Chemical constituents and cytotoxic activities from the fruits of Reevesia formosana Planta Medica. 2014 Nov;80(16):1541.
    2014-11 Chemical constituents and cytotoxic activities from the root and the stem of Reevesia formosana Planta Medica. 2014 Nov;80(16):1541.
    2013-04-13 Exploration of the role of tylophorine E ring in anti-Coronavirus activity-Tylophorine derived dibenzoquinolines impart multi-biological activities as orally active agents FASEB Journal. 2013 Apr 13;27:lb71.
    2013-04 Tylophorine induces c-Jun protein accumulation through two discrete prolonged pathways NF-kappaB/PKCdelta/JNK and PI3K/PDK1/PP2A/eEF2 to promote G1 arrest in carcinoma cells FASEB Journal. 2013 Apr;27:lb74.
    2013-04 Identification of a quinone compound inhibits human glutaminase activity and induces autophagy in carcinoma cells FASEB Journal. 2013 Apr;27:lb70.
    2009-07 Additional new 5,6-dihydroflavanones and cytotoxic constituents from the leaves of Cryptocarya chinensis Planta Medica. 2009 Jul;75(9):987-988.
    2008-07 Chemical constituents and cytotoxic activity of the root of Antidesma hiiranense Planta Medica. 2008 Jul;74(9):1076.
    2008-07 Chemical constituents from a cytotoxic root extract of Anneslea lanceolata Planta Medica. 2008 Jul;74(9):1059.
    2008-07 Secondary metabolites and cytotoxic activity of the stem bark of Litsea akoensis Planta Medica. 2008 Jul;74(9):1071.
    2008-07 Chemical constituents and cytotoxic activity of the root wood of Magnolia kachirachirai Planta Medica. 2008 Jul;74(9):1071.
    2008-07 Secondary metabolites and cytotoxic activities from the stem bark of Zanthoxylum nitidum Planta Medica. 2008 Jul;74(9):1046.
    2007-12 Tylophorine elevates the amounts of c-Jun protein in carcinoma cells ASCB 47th Annual Meeting. 2007 Dec 1-5.
    2007-04-18 Identification of novel small-molecule inhibitors of transmissible gastroenteritis virus FASEB Journal. 2007 Apr 18;21(6):LB10.
    2007-02 Anti-inflammatory effects of 7-methoxyl-cryptopleurine and structure-activity relationships of phenanthroindolizidines and phenanthroquinolizidine 第15屆細胞及分子生物新知研討會. 2007 Feb 1-3.
    2006-04 Analysis of the structure-activity relationships between phenanthroindolizidines and phenanthroquinolizidines FASEB Journal. 2006 Apr 1-5;20(5):LB492.
    2005-04 The anti-inflammatory mechanisms of [Benzothiazol-Vinyl]-benzothiazolium compounds ASIP 2005 Annual Meeting at Experimental Biology. 2005 Apr 2-6.
    Tylophorine inhibits the expression of iNOS and COX-II through AP1 in RAW264.7 Cell Stimulated by LPS/IFNγ 第13屆細胞及分子生物新知研討會. 2005 Jan 26-28.
    2004-11 Novel classes of inhibitors that suppress the nitric oxide production in RAW264.7 cells stimulated by LPS and IFN gamma Molecular Biology of the Cell. 2004 Nov;15(Suppl.S):497A.
    2004-09 Drug design of BPR0L075 as an anticancer agent World Conference on Magic Bullets - Celebrating Paul Ehrlich's 150th Birthday. 2004 Sep 9-11:Abstract # 203.
    2004-08-22 Concise synthesis and structure-activity relationships of combretastatin A-4 analogues, 1-aroylindoles and 3-aroylindoles, as novel classes of potent antitubulin agents Abstracts of Papers - American Chemical Society. 2004 Aug 22;228:U924.
    2004-07 Drug design for BPR0L075 as an anticancer agent Medicine in the 21st Century Tri-Conference & Bio-Forum 2004 Shanghai International Convention Center. 2004 Jul.
    2004-05 Suppression of nitric oxide production in activated RAW264.7 cells by Phenanthroindolizidine alkaloids FASBE Journal. 2004 May;18(8):C218.
    2003 The synthetic 1-aroylindoles and 3-aroylindoles derivatives, combretastatin A-4 analogues, as a novel class of potent anticancer agents 2003 PSROC Annual Meeting. 2003.

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