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    显示项目1-50 / 59. (共2页)
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    日期题名關聯
    2014-09 Concise syntheses of 7-anilino-indoline-N-benzenesulfonamides as antimitotic and vascular disrupting agents Bioorganic and Medicinal Chemistry. 2014 Sep;22(17):4917-4923.
    2014-08 Two new acidic diterpenoids from the heartwood of Pinus massoniana LAMB Helvetica Chimica Acta. 2014 Aug;97(8):1146-1151.
    2013-09 MPT0B098, a novel microtubule inhibitor that destabilizes the hypoxia-inducible factor-1α mrna through decreasing nuclear-cytoplasmic translocation of RNA-binding protein HuR [Erratum: Molecular Cancer Therapeutics. 2013 Jul;12(7):1202-1212.] Molecular Cancer Therapeutics. 2013 Sep;12(9):1919.
    2013-09 Furanylazaindoles: Potent anticancer agents in vitro and in vivo Journal of Medicinal Chemistry. 2013 Sep;56(20):8008-8018.
    2013-07-19 Surface alpha-enolase promotes extracellular matrix degradation and tumor metastasis and represents a new therapeutic target PLoS ONE. 2013 Jul 19;8(7):Article number e69354.
    2013-07 MPT0B098, a novel microtubule inhibitor that destabilizes the hypoxia-inducible factor-1 alpha mRNA through decreasing nuclear-cytoplasmic translocation of RNA-binding protein HuR Molecular Cancer Therapeutics. 2013 Jul;12(7):1202-1212.
    2013-06 Aconitamide, a novel alkaloid from the roots of aconitum carmichaeli Natural Product Communications. 2013 Jun;8(6):827-828.
    2013-06 Two new lignans from the wood of cunninghamia konishii Natural Product Communications. 2013 Jun;8(6):805-806.
    2013-03-15 Analgesic and anti-inflammatory bioactivities of eburicoic acid and dehydroeburicoic acid isolated from antrodia camphorata on the inflammatory mediator expression in mice Journal of Agricultural and Food Chemistry. 2013 Mar 15;61(21):5064-5071.
    2013-03-12 A novel synthetic microtubule inhibitor, MPT0B214 exhibits antitumor activity in human tumor cells through mitochondria-dependent intrinsic pathway PLoS ONE. 2013 Mar 12;8(3):Article number e58953.
    2012-12 Arginine deprivation as a new treatment strategy for head and neck cancer Oral Oncology. 2012 Dec;48(12):1227-1235.
    2012-12 An efficient, mild and scalable synthesis of bioactive compounds containing the angelicin scaffold Journal of the Chinese Chemical Society. 2012 Dec;59(12):1548-1554.
    2012-12 Application of Suzuki arylation, Sonogashira ethynylation and Rosenmund-von Braun cyanation in the exploration of substitution effects on the anticancer activity of 2-aroylquinolines Organic and Biomolecular Chemistry. 2012 Dec;10(48):9593-9600.
    2012-10 Adlay (薏苡 yi yi; “soft-shelled job’s tears”, the seeds of Coix lachryma-jobi L. var. ma-yuen Stapf) is a potential cancer chemopreventive agent toward multistage carcinogenesis processes Journal of Traditional and Complementary Medicine. 2012 Oct;2(4):267-275.
    2012-04 Targeting cathepsin S induces tumor cell autophagy via the EGFR-Erk signaling pathway Cancer Letters. 2012 Apr;317(1):89-98.
    2012-03 4-Ketopinoresinol, a novel naturally occurring ARE activator, induces the Nrf2/HO-1 axis and protects against oxidative stress-induced cell injury via activation of PI3K/AKT signaling Free Radical Biology and Medicine. 2012 Mar;52(6):1054-1066.
    2011-12-22 5-Amino-2-aroylquinolines as highly potent tubulin polymerization inhibitors. Part 2. The impact of bridging groups at position C-2 Journal of Medicinal Chemistry. 2011 Dec 22;54(24):8517-8525.
    2011-12-15 Combination of arsenic trioxide and BCNU synergistically triggers redox-mediated autophagic cell death in human solid tumors Free Radical Biology and Medicine. 2011 Dec 15;51(12):2195-2209.
    2011-10 Novel terpenoids from calocedrus macrolepis var. formosana Chemistry and Biodiversity. 2011 Oct;8(10):1901-1907.
    2011-09 Synthesis and biological evaluation of 1-(4′-Indolyl and 6′-Quinolinyl) indoles as a new class of potent anticancer agents European Journal of Medicinal Chemistry. 2011 Sep;46(9):3623-3629.
    2011-06 Antimutagenic constituents of adlay ( Coix lachryma-jobi L. var. ma-yuen Stapf) with potential cancer chemopreventive activity Journal of Agricultural and Food Chemistry. 2011 Jun;59(12):6444-6452.
    2011-06 Cytotoxic steroidal saponins from agave sisalana Planta Medica. 2011 Jun;77(9):929-933.
    2011-04-28 Scaffold-hopping strategy: Synthesis and biological evaluation of 5,6-Fused bicyclic heteroaromatics to identify orally bioavailable anticancer agents Journal of Medicinal Chemistry. 2011 Apr 28;54(8):3076-3080.
    2011-04 Concise syntheses of N-aryl-5,6,7-trimethoxyindoles as antimitotic and vascular disrupting agents: application of the copper-mediated Ullmann-type arylation Organic and Biomolecular Chemistry. 2011 Apr;9(9):3154-3157.
    2011-03-07 Synthesis and biological evaluation of 4-aroyl-6,7,8-trimethoxyquinolines as a novel class of anticancer agents Molecules. 2011 Mar 7;16(3):2274-2284.
    2011-03-07 2-Amino-3,4,5-Trimethoxybenzophenones as Potent Tubulin Polymerization Inhibitors ChemMedChem. 2011 Mar 7;6(3):450-456.
    2011-01-26 Labdanecaryophyllic acid, a novel cytotoxic C35 terpenoid from Calocedrus macrolepis var. formosana Tetrahedron Letters. 2011 Jan 26;52(4):515-517.
    2010-08 Synthesis and biological evaluation of 7-arylindoline-1-benzenesulfonamides as a novel class of potent anticancer agents MedChemComm. 2010 Aug;1(2):152-155.
    2010-06-18 Cytotoxic C35 terpenoid cryptotrione from the bark of cryptomeria japonica Organic Letters. 2010 Jun;12(12):2786-2789.
    2010-06 Design and synthesis of alpha-ketoamides as cathepsin S inhibitors with potential applications against tumor invasion and angiogenesis Journal of Medicinal Chemistry. 2010 Jun;53(11):4545-4549.
    2010-05 Chamaecypanone C, a novel skeleton microtubule inhibitor, with anticancer activity by trigger caspase 8-Fas/FasL dependent apoptotic pathway in human cancer cells Biochemical Pharmacology. 2010 May;79(9):1261-1271.
    2010-04 Arecoline arrests cells at prometaphase by deregulating mitotic spindle assembly and spindle assembly checkpoint: Implication for carcinogenesis Oral Oncology. 2010 Apr;46(4):255-262.
    2010-03-11 5-Amino-2-Aroylquinolines as Highly Potent Tubulin Polymerization Inhibitors Journal of Medicinal Chemistry. 2010 Mar 11;53(5):2309-2313.
    2009-11-01 Effects of drying and extrusion on colour, chemical composition, antioxidant activities and mitogenic response of spleen lymphocytes of sweet potatoes Food Chemistry. 2009 Nov 1;117(1):114-121.
    2009-08-13 Synthesis and evaluation of 3-aroylindoles as anticancer agents: Metabolite approach Journal of Medicinal Chemistry. 2009 Aug 13;52(15):4941-4945.
    2009-07-23 Generation of ligand-based pharmacophore model and virtual screening for identification of novel tubulin inhibitors with potent anticancer activity Journal of Medicinal Chemistry. 2009 Jul 23;52(14):4221-4233.
    2009-07-03 Survivin counteracts the therapeutic effect of microtubule de-stabilizers by stabilizing tubulin polymers Molecular Cancer. 2009 Jul 3;8:Article number 43.
    2009-04-17 Synthesis and structure-activity relationships of 1-benzyl-4,5,6-trimethoxyindoles as a novel class of potent antimitotic agents ChemMedChem. 2009 Apr 17;4(4):588-593.
    2008-12-25 Synthesis and structure-activity relationships of 2-amino-1-aroylnaphthalene and 2-hydroxy-1-aroylnaphthalenes as potent antitubulin agents Journal of Medicinal Chemistry. 2008 Dec 25;51(24):8163-8167.
    2008-08 Transcriptional repression of O-6-methylguanine DNA methyltransferase gene rendering cells hypersensitive to N,N '-bis(2-chloroethyl)-N-nitrosurea in camptothecin-resistant cells Molecular Pharmacology. 2008 Aug;74(2):517-526.
    2008-07-24 Discovery of 4-amino and 4-hydroxy-1-aroylindoles as potent tubulin polymerization inhibitors Journal of Medicinal Chemistry. 2008 Jul;51(14):4351-4355.
    2008-02 A novel peroxisome proliferator-activated receptor alpha/gamma agonist, BPR1H0101, inhibits topoisomerase II catalytic activity in human cancer cells Anti-Cancer Drugs. 2008 Feb;19(2):151-158.
    2007-11-15 Tamoxifen accelerates proteasomal degradation of O-6-methylguanine DNA methyltransferase in human cancer cells International Journal of Cancer. 2007 Nov;121(10):2293-2300.
    2007-10 A novel oral indoline-sulfonamide agent, N-[1-(4-Methoxy-benzenesulfonyl)-2,3-dihydro-1H-indol-7-yl]-Isonicotinamide (J30), exhibits potent activity against human cancer cells in vitro and in vivo through the disruption of microtubule Journal of Pharmacology and Experimental Therapeutics. 2007 Oct;323(1):398-405.
    2007-09-06 4-and 5-aroylindoles as novel classes of potent antitubulin agents Journal of Medicinal Chemistry. 2007 Sep;50(18):4548-4552.
    2007-07-31 Combined modalities of resistance in an oxaliplatin-resistant human gastric cancer cell line with enhanced sensitivity to 5-fluorouracil British Journal of Cancer. 2007 Jul;97(3):334-344.
    2007-02-26 Cytotoxic and novel skeleton compounds from the heartwood of Chamaecyparis obtusa var. formosana Tetrahedron Letters. 2007 Feb;48(9):1567-1569.
    2007-01 D-501036, a novel selenophene-based triheterocycle derivative, exhibits potent in vitro and in vivo antitumoral activity which involves DNA damage and ataxia telangiectasia-mutated nuclear protein kinase activation Molecular Cancer Therapeutics. 2007 Jan;6(1):193-202.
    2006-11-27 C-35 terpenoids from the bark of Calocedrus macrolepis var. formosana with activity against human cancer cell lines Journal of Natural Products. 2006 Nov;69(11):1611-1613.
    2006-11-16 7-aroyl-aminoindoline-1-sulfonamides as a novel class of potent antitubulin agents Journal of Medicinal Chemistry. 2006 Nov;49(23):6656-6659.

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