邻近类别 報告 [0/1] 專利 [0/82] 期刊論文 [110/110] 类别统计 近3年内发表的文件:0(0.00%) 含全文笔数:10(52.63%) 文件下载次数统计 下载大于0次:10(100.00%) 下载大于100次:10(100.00%) 全文下载总次数:6670(6.74%) 最后更新时间: 2024-11-28 16:44 上传排行 数据加载中..... 下载排行 数据加载中..... 最近上传 BPRDP056, a novel small molecule dr... Development drug candidate targetin... 3D-QSAR assisted drug design: Ident... Design and synthesis of Aurora kina... Design, synthesis, and SAR studies ... BPR000K, a novel Aurora kinase inhi... Identification of a quinone compoun... Exploration of the role of tylophor... Tylophorine induces c-Jun protein a... BPR1J271, a novel FLT3 inhibitor fo...

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日期	题名	關聯
2019-07	BPRDP056, a novel small molecule drug conjugate specifically targeting phosphatidylserine for cancer therapy	Cancer Research. 2019 Jul;79(13, Suppl.):Abstract number 227.
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.
2013-04-07	BPR000K, a novel Aurora kinase inhibitor	Abstracts of Papers - American Chemical Society. 2013 Apr 7;245:Article number 300-MEDI.
2013-04-07	3D-QSAR assisted drug design: Identification of a potent quinazoline based Aurora kinase inhibitor	Abstracts of Papers - American Chemical Society. 2013 Apr 7;245:Article number 87-MEDI.
2013-04-07	Development drug candidate targeting EGFR kinase: DBPR112	Abstracts of Papers - American Chemical Society. 2013 Apr 7;245:Article number 299-MEDI.
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.
2013-04	Design and synthesis of Aurora kinase inhibitors as anticancer agents	Abstracts of Papers - American Chemical Society. 2013 Apr;245:Article number 301-MEDI.
2012-11	BPR1J271, a novel FLT3 inhibitor for treating acute myeloid leukemia	European Journal of Cancer. 2012 Nov;48(Suppl. 6):53-54.
2012-03-25	Design, synthesis, and SAR studies of duel FLT-3 and Aurora kinase inhibitors	Abstracts of Papers - American Chemical Society. 2012 Mar 25;243:Article number 48-MEDI.
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.
2011-03-27	Design and synthesis of potent Aurora kinase inhibitors	Abstracts of Papers - American Chemical Society. 2011 Mar 27;241:258-MEDI.
2010-08	Lead optimization of furanopyrimidine Aurora kinase inhibitors: Development of in vivo active agents in tumor xenograft models	Abstracts of Papers - American Chemical Society. 2010 Aug;240:MEDI 332.
2009-09	Fast-forwarding kinase drug discovery: aurora and EGFR kinase inhibitor lead development	EJC Supplements. 2009 Sep;7(2):96.
2007-07	Anti-influenza drug discovery	Drugs of the Future. 2007 Jul;32(Suppl. A):97.
2007-04-18	Identification of novel small-molecule inhibitors of transmissible gastroenteritis virus	FASEB Journal. 2007 Apr 18;21(6):LB10.
2005-03	Design and structure-activity relationships of novel indole-based PPAR agonists as antidiabetic agents	Abstracts of Papers of the American Chemical Society. 2005 Mar;229(Part 2):U141.
2005-03	Design, synthesis and sar of indole-based PPAR agonists	Abstracts of Papers of the American Chemical Society. 2005 Mar;229(Part 2):U141.

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