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生技與藥物研究所
伍素瑩
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夏克山
[
76
/98]
岳嶽
[
29
/32]
張仲明
[
7
/9]
張俊彥
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18
/18]
張竣評
[
21
/26]
徐祖安
[
170
/215]
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
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/24]
莊宏
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/1]
葉修華
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24
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葉燈光
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133
/152]
蔣維棠
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41
/66]
謝興邦
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171
/231]
趙宇生(2002-2013)
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120
/212]
郭靜娟
[
49
/55]
鄒倫
[
28
/29]
陳志豪
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31
/52]
陳新(2002-2015)
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53
/67]
陳炯東
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180
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顏婉菁
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/7]
許明珠(1997-2001)
[
3
/10]
陳淑貞(1998-2001)
[
3
/11]
陳華鍵(1997-2001)
[
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/9]
Community Statistics
近3年內發表的文件:1(1.54%)
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最後更新時間: 2024-12-01 02:01
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Showing items 51-65 of 65. (2 Page(s) Totally)
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Date
Title
Relation
2008-07-01
Pyrrolidine compounds
KR10-0844593/2008-07-01
2008-03-01
Aurora kinase A inhibitors: Identification, SAR exploration and molecular modeling of 6,7-dihydro-4H-pyrazolo-[1,5-a]pyrrolo[3,4-d]pyrimidine-5,8-dione scaffold
Bioorganic and Medicinal Chemistry Letters. 2008 Mar;18(5):1623-1627.
2008
Structure-based inhibitors exhibit differential activities against Helicobacter pylori and Escherichia coli undecaprenyl pyrophosphate synthases
Journal of Biomedicine and Biotechnology. 2008; 2008:Article number 841312.
2007
Crystal structures and computer screened inhibitors of Helicobacter pylori undecaprenyl pyrophosphate synthase
Frontiers in the Convergence of Bioscience and Information Technologies, FBIT 2007. 2007:305-310(Article number 4524124).
2006-10-19
Structural basis for the structure-activity relationships of peroxisome proliferator-activated receptor agonists
Journal of Medicinal Chemistry. 2006 Oct;49(21):6421-6424.
2006-08-24
Structure-based drug design and structural biology study of novel nonpeptide inhibitors of severe acute respiratory syndrome coronavirus main protease
Journal of Medicinal Chemistry. 2006 Aug;49(17):5154-5161.
2006-06-15
Discovery of a novel family of SARS-CoV protease inhibitors by virtual screening and 3D-QSAR studies
Journal of Medicinal Chemistry. 2006 Jun;49(12):3485-3495.
2006-05-04
Structure-based drug design of a novel family of PPAR gamma partial agonists: Virtual screening, X-ray crystallography, and in vitro/in vivo biological activities
Journal of Medicinal Chemistry. 2006 May;49(9):2703-2712.
2006-02-09
Indol-1-yl acetic acids as peroxisome proliferator-activated receptor agonists: Design, synthesis, structural biology, and molecular docking studies
Journal of Medicinal Chemistry. 2006 Feb;49(3):1212-1216.
2006-01-12
2-[3-[2-[(2S)-2-cyano-1-pyrrolidinyl]-2-oxoethylamino]-3-methyl-1-oxobutyl]-1,2,3,4-tetrahydroisoquinoline: A potent, selective, and orally bioavailable dipeptide-derived inhibitor of dipeptidyl peptidase IV
Journal of Medicinal Chemistry. 2006 Jan;49(1):373-380.
2005-12-29
Novel indole-based peroxisome proliferator-activated receptor agonists: Design, SAR, structural biology, and biological activities
Journal of Medicinal Chemistry. 2005 Dec;48(26):8194-8208.
2005-12-15
The effect of N-terminal truncation on double-dimer assembly of goose delta-crystallin
Biochemical Journal. 2005 Dec;392(Pt. 3):545-554.
2005-07-01
Glutamic acid analogues as potent dipeptidyl peptidase IV and 8 inhibitors
Bioorganic and Medicinal Chemistry Letters. 2005 Jul;15(13):3271-3275.
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.
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.
Showing items 51-65 of 65. (2 Page(s) Totally)
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