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Two new acidic diterpenoids from th...
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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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