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生技與藥物研究所
趙宇生(2002-2013)
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趙宇生(2002-2013)
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報告
[
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專利
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/82]
期刊論文
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110
/110]
會議論文/會議摘要
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10
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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]
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
[
22
/24]
莊宏
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1
/1]
葉修華
[
24
/25]
葉燈光
[
133
/152]
蔣維棠
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41
/66]
謝興邦
[
171
/231]
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:1(0.47%)
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最後更新時間: 2024-11-28 13:41
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Selective and antagonist-dependent ...
DBPR108, a novel dipeptidyl peptida...
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Targeting coronaviral replication a...
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Showing items 1-25 of 212. (9 Page(s) Totally)
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Date
Title
Relation
2022-11
Selective and antagonist-dependent µ-opioid receptor activation by the combination of 2-{[2-(6-chloro-3,4-dihydro-1(2H)-quinolinyl)-2-oxoethyl]sulfanyl}-5-phenyl-4,6-(1H,5H)-pyrimidinedione and naloxone/naltrexone
Bioorganic Chemistry. 2022 Nov;128:Article number 105905.
2021-08-01
DBPR108, a novel dipeptidyl peptidase-4 inhibitor with antihyperglycemic activity
Life Sciences. 2021 Aug 1;278:Article number 119574.
2021-01
BPRDP056, a novel small molecule drug conjugate specifically targeting phosphatidylserine for cancer therapy
Translational Oncology. 2021 Jan;14(1):Article number 100897.
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.
2019-04-01
A novel, potent, and orally bioavailable thiazole HCV NS5A inhibitor for the treatment of hepatitis C virus
European Journal of Medicinal Chemistry. 2019 Apr 1;167:245-268.
2019-04-01
The in vivo antinociceptive and mu-opioid receptor activating effects of the combination of N-phenyl-2′,4′-dimethyl-4,5′-bi-1,3-thiazol-2-amines and naloxone
European Journal of Medicinal Chemistry. 2019 Apr 1;167:312-323.
2019-03
Synthesis and biological evaluation of N-glucosyl indole derivatives as sodium-dependent glucose co-transporter 2 inhibitors
Bioorganic Chemistry. 2019 Mar;83:520-525.
2018-04
4-Bromophenylhydrazinyl benzenesulfonylphenylureas as indoleamine 2,3-dioxygenase inhibitors with in vivo target inhibition and anti-tumor efficacy
Bioorganic Chemistry. 2018 Apr;77:600-607.
2018-01-01
Identification of an oxime-containing C-glucosylarene as a potential inhibitor of sodium-dependent glucose co-transporter 2
European Journal of Medicinal Chemistry. 2018 Jan 1;143:611-620.
2017-06-22
Targeting coronaviral replication and cellular JAK2 mediated dominant NF-kappaB activation for comprehensive and ultimate inhibition of coronaviral activity
Scientific Reports. 2017 Jun 22;7:Article number 4105.
2017-01
A potent, selective, and orally bioavailable HCV NS5A inhibitor for treatment of Hepatitis C Virus: (S)-1-((R)-2-(Cyclopropanecarboxamido)-2-phenylacetyl)-N-(4-phenylthiazo l-2-yl)pyrrolidine-2-carboxamide
Journal of Medicinal Chemistry. 2017 Jan;60(1):228-247.
2016-05
N-Indolylglycosides bearing modifications at the glucose C6-Position as Sodium-Dependent Glucose Co-transporter 2 inhibitors
Bioorganic and Medicinal Chemistry. 2016 May;24(10):2242-2250.
2016-01
Phenyl benzenesulfonylhydrazides exhibit selective Indoleamine 2,3-Dioxygenase inhibition with potent in vivo pharmacodynamic activity and antitumor efficacy
Journal of Medicinal Chemistry. 2016 Jan;59(1):419-430.
2015-07-31
作為極光激酶抑制劑的稠合雙環嘧啶化合物
HK1151694/2015-07-31
2015-07-29
脯氨酸衍生物
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2015-07-22
作为酪胺酸激酶抑制剂的稠合双环及多环嘧啶化合物
ZL200980144458.1/2015-07-22
2015-07
Development and application of a fluorescent glucose uptake assay for the high-throughput screening of non-glycoside SGLT2 inhibitors
European Journal of Pharmaceutical Sciences. 2015 Jul;74:40-44.
2015-07
Pharmacological induction of human fetal globin gene in hydroxyurea-resistant primary adult erythroid cells
Molecular and Cellular Biology. 2015 Jul;35(14):2541-2553.
2015-07
Identification of a potent 5-phenyl-thiazol-2-ylamine-based inhibitor of FLT3 with activity against drug resistance-conferring point mutations
European Journal of Medicinal Chemistry. 2015 Jul;100:151-161.
2015-06-01
治療C型肝炎病毒感染之醫藥組成物
I486160/2015-06-01
2015-05-29
Proline derivatives
JP5753185/2015-05-29
2015-05
A novel peripheral cannabinoid receptor 1 antagonist, BPR0912, reduces weight independently of food intake and modulates thermogenesis
Diabetes, Obesity and Metabolism. 2015 May;17(5):495-504.
2015-04-14
Fused multicyclic compounds as protein kinase inhibitors
US9006252B2/2015-04-14
2015-02-24
Pyrazole compounds
US8962845/2015-02-24
2015-02-11
吡唑類化合物
I472514/2015-02-11
Showing items 1-25 of 212. (9 Page(s) Totally)
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