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显示项目111-120 / 215. (共22页) << < 7 8 9 10 11 12 13 14 15 16 > >> 每页显示[10|25|50]项目

日期	题名	關聯
2012-01	BPR1J-097, a novel FLT3 kinase inhibitor, exerts potent inhibitory activity against AML	British Journal of Cancer. 2012 Jan;106(3):475-481.
2012-01	A High-throughput cell-based screening for L858R/T790M mutant epidermal growth factor receptor inhibitors	Anticancer Research. 2012 Jan;32(1):147-151.
2011-12	Development of a whole-cell screening system for evaluation of the human CYP1A2-mediated metabolism	Biotechnology and Bioengineering. 2011 Dec;108(12):2932-2940.
2011-09-23	BPR1K653, a novel Aurora Kinase Inhibitor, exhibits potent anti-proliferative activity in P-gp170 (MDR1)-mediated VX680-resistant cancer cells in vitro and in vivo	European Journal of Cancer. 2011 Sep 23;47:S127.
2011-09	Overcoming the acquired resistance to Afatinib (BIBW2992) in HCC827, a non-small cell lung cancer cell line	European Journal of Cancer. 2011 Sep;47:S129.
2011-09	Suppression of stat3 activity sensitizes gefitinib-resistant non small cell lung cancer cells	European Journal of Cancer. 2011 Sep;47(Suppl. 1):S104.
2011-08	BPR1K653, a novel aurora kinase inhibitor, exhibits potent anti-proliferative activity in MDR1 (P-gp170)-mediated multidrug-resistant cancer cells	PLoS ONE. 2011 Aug;6(8):Article number e23485.
2011-07-26	Hepatitis C virus inhibitors	US7985763B2/2011-07-26
2011-07-11	抑制C型肝炎病毒感染之倍半帖內酯類化合物及其醫藥組成物	I344959/2011-07-11
2011-07	Discovery and evaluation of 3-phenyl-1H-5-pyrazolylamine-based derivatives as potent, selective and efficacious inhibitors of FMS-like tyrosine kinase-3 (FLT3)	Bioorganic and Medicinal Chemistry. 2011 Jul;19(14):4173-4182 .

显示项目111-120 / 215. (共22页) << < 7 8 9 10 11 12 13 14 15 16 > >> 每页显示[10|25|50]项目