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生技與藥物研究所
徐祖安
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專利
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0
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期刊論文
[
143
/144]
會議論文/會議摘要
[
27
/39]
Siblings
伍素瑩
[
52
/65]
其他
[
58
/60]
夏克山
[
76
/98]
岳嶽
[
29
/32]
張仲明
[
7
/9]
張俊彥
[
18
/18]
張竣評
[
21
/26]
李秀珠
[
75
/105]
李靜琪
[
23
/24]
林書玉
[
19
/20]
洪明秀
[
31
/40]
潘秀玲(2009-2013)
[
16
/17]
王文傑
[
13
/15]
王鴻俊
[
7
/7]
石全(2014-2017)
[
35
/39]
童俊維
[
23
/23]
紀雅惠
[
21
/25]
翁紹華
[
22
/24]
莊宏
[
1
/1]
葉修華
[
24
/25]
葉燈光
[
133
/152]
蔣維棠
[
41
/66]
謝興邦
[
171
/231]
趙宇生(2002-2013)
[
120
/212]
郭靜娟
[
49
/55]
鄒倫
[
28
/29]
陳志豪
[
31
/52]
陳新(2002-2015)
[
53
/67]
陳炯東
[
180
/212]
顏婉菁
[
6
/7]
許明珠(1997-2001)
[
3
/10]
陳淑貞(1998-2001)
[
3
/11]
陳華鍵(1997-2001)
[
9
/9]
Community Statistics
近3年內發表的文件:9(4.19%)
含全文筆數:170(79.07%)
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下載大於100次:168(98.82%)
檔案下載總次數:103261(1.93%)
最後更新時間: 2024-12-01 00:41
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Showing items 101-125 of 215. (9 Page(s) Totally)
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Date
Title
Relation
2012-06-07
3-Phenyl-1H-5-pyrazolylamine-based derivatives as potent and efficacious inhibitors of FMS-like tyrosine kinase-3 (FLT3)
Bioorganic and Medicinal Chemistry Letters. 2012 Jun 7;22(14):4654-4659.
2012-06
EGFR and myosin II inhibitors cooperate to suppress EGFR-T790M-mutant NSCLC cells
Molecular Oncology. 2012 Jun;6(3):299-310.
2012-05-11
作為極光激酶抑制劑之稠合雙環嘧啶化合物
I363627/2012-05-11
2012-04-11
咪唑啉酮及咪唑啉硫酮衍生物
I361808/2012-04-11
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.
2012-03-20
Fused bicyclic pyrimidine compounds as aurora kinase inhibitors
US8138194B2/2012-03-20
2012-03-01
C型肝炎病毒抑制劑
I359137/2012-03-01
2012-02
Synthesis and biological evaluation of 2-amino-1-thiazolyl imidazoles as orally active anticancer agents
Investigational New Drugs. 2012 Feb;30(1):164-175.
2012-02
Identification of BPR3P0128 as an Inhibitor of cap-snatching activities of influenza virus
Antimicrobial Agents and Chemotherapy. 2012 Feb;56(2):647-657.
2012-01
Resistance analysis and characterization of a thiazole analogue, BP008, as a potent hepatitis C virus NS5A inhibitor
Antimicrobial Agents and Chemotherapy. 2012 Jan;56(1):44-53.
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 .
2011-06-21
抑制冠狀病毒之醫藥組合物
I343809/2011-06-21
2011-06-21
抑制冠狀病毒之醫藥組合物
I343808/2011-06-21
2011-06-21
抑制冠狀病毒之醫藥組合物
I343810/2011-06-21
2011-06-01
Suppression of Stat3 activity sensitizes gefitinib-resistant non small cell lung cancer cells
Biochemical Pharmacology. 2011 Jun 01;81(11):1263-1270.
2011-06
Synergistic inhibition of enterovirus 71 replication by interferon and rupintrivir
Journal of Infectious Diseases. 2011 Jun;203(12):1784-1790.
Showing items 101-125 of 215. (9 Page(s) Totally)
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