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    Patents [0/113]
    Periodical Articles [110/110]
    Conference Papers/Meeting Abstract [10/19]

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    Showing items 1-50 of 242. (5 Page(s) Totally)
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    DateTitleRelation
    2024-03-26 Heterocyclic compounds and use thereof NZ730195/2024-03-26
    2023-12-19 Heterocyclic compounds and use thereof CA2962329/2023-12-19
    2023-09-26 Composto de fórmula (i) e composição farmacêutica BR112017005713/2023-09-26
    2023-03-08 헤테로사이클릭 화합물과 이의 용도 KR10-2509431/2023-03-08
    2023-02-10 Heterocyclic compounds and use thereof IN421151/2023-02-10
    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.
    2022-01-07 雜環化合物及其用途 HK1238644/2022-01-07
    2022-01-05 雜環化合物及其用途 J/005468/2022-01-05
    2021-09-10 杂环化合物及其用途 CN107207465/2021-09-10
    2021-08-29 Pyrazole compounds AE3821/2021-08-29
    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.
    2020-02-13 Heterocyclic compounds and use thereof AU2015321654/2020-02-13
    2019-11-15 複素環式化合物及びその使用 JP6615207/2019-11-15
    2019-10-23 Heterocyclic compounds and use thereof RU2704008/2019-10-23
    2019-10-22 Compostos e composição farmacêutica BR112013013490/2019-10-22
    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.
    2018-11-07 Pyrazole compounds EP2632919/2018-11-07
    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.
    2018-03-29 吡唑類化合物 HK1187610/2018-03-29
    2018-03-27 Heterocyclic compounds and use thereof US9926298/2018-03-27
    2018-01-09 Heterocyclic compounds and use thereof US9862703/2018-01-09
    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.
    2017-09-11 雜環化合物及其用途 TWI598348/2017-09-11
    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.
    2017-02-01 티로신 키나아제 억제제로서의 접합 이환 및 삼환 피리미딘 화합물 KR10-1703941/2017-02-01
    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.
    2016-11-23 吡唑類化合物 J/002325/2016-11-23
    2016-10-27 Pyrazole derivatives RU2600983/2016-10-27
    2016-06-22 吡唑类化合物 CN103459383/2016-06-22
    2016-06-09 Pyrazole compounds AU2012316331/2016-06-09
    2016-05-10 Pyrazole compounds CA2818944/2016-05-10
    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.
    2016-02-19 作為酪胺酸激酶抑制劑的稠合雙環及多環嘧啶化合物 HK1162509/2016-02-19
    2016-02-04 作爲酪胺酸激酶抑制劑的稠合雙環及多環嘧啶化合物 J/001914/2016-02-04
    2016-01-22 ピラゾール化合物 JP5872591/2016-01-22
    2016-01-13 피라졸 화합물 KR10-1586714/2016-01-13
    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 CN102482269/2015-07-29
    2015-07-24 チロシンキナーゼ阻害剤としての融合2環および3環ピリミジン化合物 JP5781934/2015-07-24
    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 CN102264745/2015-07-22
    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 TWI486160/2015-06-01
    2015-05-29 Proline derivatives JP5753185/2015-05-29

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