臺大學術典藏 |
2022-03-09T02:18:56Z |
Optimization and development of selective histone deacetylase inhibitor (Mpt0b291)-loaded albumin nanoparticles for anticancer therapy
|
Putri A.D.; PAI-SHAN CHEN; Su Y.-L.; Lin J.-P.; Liou J.-P.; Hsieh C.-M. |
國立成功大學 |
2022 |
HDAC6 involves in regulating the lncRNA-microRNA-mRNA network to promote the proliferation of glioblastoma cells
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Wu, A.-C.;Yang, W.-B.;Chang, K.-Y.;Lee, J.-S.;Liou, J.-P.;Su, R.-Y.;Cheng, S.M.;Hwang, D.-Y.;Kikkawa, U.;Hsu, T.-I.;Wang, C.-Y.;Chang, W.-C.;Chen, P.-Y.;Chuang, J.-Y. |
臺大學術典藏 |
2021-07-07T05:13:16Z |
Novel radical synthesis of morphine fragments spiro[benzofuran-3(2H),4'-piperidine] and octahydro-1H-benzofuro[3,2-e]isoquinoline
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Cheng C.-Y.; LING-WEI HSIN; Liou J.-P. |
臺大學術典藏 |
2021-06-04T08:33:27Z |
1-Arylsulfonyl-5-(N-hydroxyacrylamide)indolines Histone Deacetylase Inhibitors Are Potent Cytokine Release Suppressors
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Lee H.-Y.; CHIA-RON YANG; Lai M.-J.; Huang H.-L.; Hsieh Y.-L.; Liu Y.-M.; Yeh T.-K.; Li Y.-H.; Mehndiratta S.; Teng C.-M.; Liou J.-P. |
臺大學術典藏 |
2021-06-04T08:33:27Z |
Inside Cover: 1-Arylsulfonyl-5-(N-hydroxyacrylamide)indolines Histone Deacetylase Inhibitors Are Potent Cytokine Release Suppressors (ChemBioChem 10/2013)
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Lee H.-Y.; CHIA-RON YANG; Lai M.-J.; Huang H.-L.; Hsieh Y.-L.; Liu Y.-M.; Yeh T.-K.; Li Y.-H.; Mehndiratta S.; Teng C.-M.; Liou J.-P. |
臺大學術典藏 |
2021-06-04T08:33:27Z |
Anti-Arthritic effects of magnolol in human interleukin 1β-Stimulated Fibroblast-Like synoviocytes and in a rat arthritis model
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Wang J.-H.; Shih K.-S.; Liou J.-P.; Wu Y.-W.; Chang A.S.-Y.; Wang K.-L.; Tsai C.-L.; CHIA-RON YANG |
臺大學術典藏 |
2021-06-04T08:33:26Z |
Denbinobin upregulates miR-146a expression and attenuates IL-1β-induced upregulation of ICAM-1 and VCAM-1 expressions in osteoarthritis fibroblast-like synoviocytes
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CHIA-RON YANG; Shih K.-S.; Liou J.-P.; Wu Y.-W.; Hsieh I.-N.; Lee H.-Y.; Lin T.-C.; Wang J.-H. |
臺大學術典藏 |
2021-06-04T08:33:25Z |
Indole-3-ethylsulfamoylphenylacrylamides: Potent histone deacetylase inhibitors with anti-inflammatory activity
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Mehndiratta S.; Hsieh Y.-L.; Liu Y.-M.; Wang A.W.; Lee H.-Y.; Liang L.-Y.; Kumar S.; Teng C.-M.; CHIA-RON YANG; Liou J.-P. |
臺大學術典藏 |
2021-06-04T08:33:25Z |
Preclinical anti-arthritic study and pharmacokinetic properties of a potent histone deacetylase inhibitor MPT0G009
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Hsieh I.-N.; Liou J.-P.; Lee H.-Y.; Lai M.-J.; Li Y.-H.; CHIA-RON YANG |
臺大學術典藏 |
2021-06-04T08:33:25Z |
Anticancer activity of MPT0G157, a derivative of indolylbenzenesulfonamide, inhibits tumor growth and angiogenesis
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Huang Y.-C.; Huang F.-I.; Mehndiratta S.; Lai S.-C.; Liou J.-P.; CHIA-RON YANG |
臺大學術典藏 |
2021-06-04T08:33:24Z |
An oral quinoline derivative, MPT0B392, causes leukemic cells mitotic arrest and overcomes drug resistant cancer cells
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Chao M.-W.;Huang H.-L.;Huangfu W.-C.;Hsu K.-C.;Liu Y.-M.;Wu Y.-W.;Lin C.-F.;Chen Y.-L.;Lai M.-J.;Lee H.-Y.;Liou J.P.;Teng C.-M.;Chia-Ron Yang; Chao M.-W.; Huang H.-L.; HuangFu W.-C.; Hsu K.-C.; Liu Y.-M.; Wu Y.-W.; Lin C.-F.; Chen Y.-L.; Lai M.-J.; Lee H.-Y.; Liou J.P.; Teng C.-M.; CHIA-RON YANG |
臺大學術典藏 |
2021-06-04T08:33:24Z |
3-Aroylindoles display antitumor activity in?vitro and in?vivo: Effects of N1-substituents on biological activity
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Lee H.-Y.;Lee J.-F.;Kumar S.;Wu Y.-W.;Huangfu W.-C.;Lai M.-J.;Li Y.-H.;Huang H.-L.;Kuo F.-C.;Hsiao C.-J.;Cheng C.-C.;Chia-Ron Yang;Liou J.-P.; Lee H.-Y.; Lee J.-F.; Kumar S.; Wu Y.-W.; HuangFu W.-C.; Lai M.-J.; Li Y.-H.; Huang H.-L.; Kuo F.-C.; Hsiao C.-J.; Cheng C.-C.; CHIA-RON YANG; Liou J.-P. |
臺大學術典藏 |
2021-06-04T08:33:24Z |
Novel histone deacetylase inhibitor MPT0G009 induces cell apoptosis and synergistic anticancer activity with tumor necrosis factor-related apoptosis-inducing ligand against human hepatocellular carcinoma
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Chen M.-C.; Huang H.-H.; Lai C.-Y.; Lin Y.-J.; Liou J.-P.; Lai M.-J.; Li Y.-H.; Teng C.-M.; CHIA-RON YANG |
臺大學術典藏 |
2021-06-04T08:33:24Z |
2-(Phenylsulfonyl)quinoline N-hydroxyacrylamides as potent anticancer agents inhibiting histone deacetylase
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Lee H.-Y.; Chang C.-Y.; Su C.-J.; Huang H.-L.; Mehndiratta S.; Chao Y.-H.; Hsu C.-M.; Kumar S.; Sung T.-Y.; Huang Y.-Z.; Li Y.-H.; CHIA-RON YANG; Liou J.-P. |
臺大學術典藏 |
2021-06-04T08:33:23Z |
(N-Hydroxycarbonylbenylamino)quinolines as Selective Histone Deacetylase 6 Inhibitors Suppress Growth of Multiple Myeloma in Vitro and in Vivo
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Lee H.-Y.; Nepali K.; Huang F.-I.; Chang C.-Y.; Lai M.-J.; Li Y.-H.; Huang H.-L.; CHIA-RON YANG; Liou J.-P. |
臺大學術典藏 |
2021-06-04T08:33:23Z |
Anti-leukemia effects of the novel synthetic 1-benzylindole derivative 21-900 in vitro and in vivo
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Huangfu W.-C.; Chao M.-W.; Cheng C.-C.; Wei Y.-C.; Wu Y.-W.; Liou J.-P.; Hsiao G.; Lee Y.-C.; CHIA-RON YANG |
臺大學術典藏 |
2021-06-04T08:33:22Z |
MPT0G413, A novel HDAC6-selective inhibitor, and bortezomib synergistically exert anti-tumor activity in multiple myeloma cells
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Huang F.-I.;Wu Y.-W.;Sung T.-Y.;Liou J.-P.;Lin M.-H.;Pan S.-L.;Chia-Ron Yang; Huang F.-I.; Wu Y.-W.; Sung T.-Y.; Liou J.-P.; Lin M.-H.; Pan S.-L.; CHIA-RON YANG |
臺大學術典藏 |
2021-06-04T08:33:22Z |
The anticancer effects of MPT0G211, a novel HDAC6 inhibitor, combined with chemotherapeutic agents in human acute leukemia cells
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Tu H.-J.; Lin Y.-J.; Chao M.-W.; Sung T.-Y.; Wu Y.-W.; Chen Y.-Y.; Lin M.-H.; Liou J.-P.; Pan S.-L.; CHIA-RON YANG |
臺大學術典藏 |
2021-06-04T08:33:22Z |
5-Aroylindoles Act as Selective Histone Deacetylase 6 Inhibitors Ameliorating Alzheimer's Disease Phenotypes
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Lee H.-Y.; Fan S.-J.; Huang F.-I.; Chao H.-Y.; Hsu K.-C.; Lin T.E.; Yeh T.-K.; Lai M.-J.; Li Y.-H.; Huang H.-L.; CHIA-RON YANG; Liou J.-P. |
臺大學術典藏 |
2021-06-04T08:33:22Z |
The novel histone de acetylase 6 inhibitor, MPT0G211, ameliorates tau phosphorylation and cognitive deficits in an Alzheimer's disease model article
|
Fan S.-J.; Huang F.-I.; Liou J.-P.; CHIA-RON YANG |
臺大學術典藏 |
2021-06-04T08:33:21Z |
Anti-metastatic activity of MPT0G211, a novel HDAC6 inhibitor, in human breast cancer cells in vitro and in vivo
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Hsieh Y.-L.;Tu H.-J.;Pan S.-L.;Liou J.-P.;Chia-Ron Yang; Hsieh Y.-L.; Tu H.-J.; Pan S.-L.; Liou J.-P.; CHIA-RON YANG |
臺大學術典藏 |
2021-06-04T08:33:19Z |
A novel dual HDAC and HSP90 inhibitor, MPT0G449, downregulates oncogenic pathways in human acute leukemia in vitro and in vivo
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Wu Y.-W.; Chao M.-W.; Tu H.-J.; Chen L.-C.; Hsu K.-C.; Liou J.-P.; CHIA-RON YANG; Yen S.-C.; HuangFu W.-C.; Pan S.-L. |
臺大學術典藏 |
2021-05-18T01:38:04Z |
HDAC inhibitor protects chronic cerebral hypoperfusion and oxygen-glucose deprivation injuries via H3K14 and H4K5 acetylation-mediated BDNF expression
|
Fang Y.-C.;Chan L.;Liou J.-P.;Yong-Kwang Tu;Lai M.-J.;Chen C.-I.;Vidyanti A.N.;Lee H.-Y.;Hu C.-J.; Fang Y.-C.; Chan L.; Liou J.-P.; YONG-KWANG TU; Lai M.-J.; Chen C.-I.; Vidyanti A.N.; Lee H.-Y.; Hu C.-J. |
臺大學術典藏 |
2021-05-18T01:38:04Z |
Protective effects of 10,11-dihydro-5H-dibenzo[b,f]azepine hydroxamates on vascular cognitive impairment
|
Kaur N.; Fang Y.-C.; Lee H.-Y.; Singh A.; Nepali K.; Lin M.-H.; Yeh T.-K.; Lai M.-J.; Chan L.; YONG-KWANG TU; Banerjee S.; Hu C.-J.; Liou J.-P. |
臺大學術典藏 |
2020-07-01T07:18:19Z |
Intermediary metabolite precursor dimethyl-2-ketoglutarate stabilizes hypoxia-inducible factor-1α by inhibiting prolyl-4-hydroxylase PHD2
|
Hou P.;Ching-Ying Kuo;Cheng C.-T.;Liou J.-P.;Ann D.K.;Chen Q.; Hou P.; CHING-YING KUO; Cheng C.-T.; Liou J.-P.; Ann D.K.; Chen Q. |
臺大學術典藏 |
2018-09-10T09:41:13Z |
The HDAC inhibitor, MPT0E028, enhances erlotinib-induced cell death in EGFR-TKI-resistant NSCLC cells
|
Chen, M.-C.;Chen, C.-H.;Wang, J.-C.;Tsai, A.-C.;Liou, J.-P.;Pan, S.-L.;Teng, C.-M.; CHE-MING TENG |
臺大學術典藏 |
2018-09-10T05:45:17Z |
Novel radical synthesis of morphine fragments spiro[benzofuran-3(2H),4'-piperidine] and octahydro-1H-benzofuro[3,2-e]isoquinoline
|
Cheng, C.-Y.;Hsin, L.-W.;Liou, J.-P.; LING-WEI HSIN |
國立成功大學 |
2017 |
Specificity protein 1-modulated superoxide dismutase 2 enhances temozolomide resistance in glioblastoma, which is independent of O6-methylguanine-DNA methyltransferase
|
Chang, K.-Y.;Hsu, T.-I.;Hsu, C.-C.;Tsai, S.-Y.;Liu, J.-J.;Chou, S.-W.;Liu, M.-S.;Liou, J.-P.;Ko, C.-Y.;Chen, K.-Y.;Hung, J.-J.;Chang, W.-C.;Chuang, Chuang C.-K.;Kao, T.-J.;Chuang, J.-Y. |
國立成功大學 |
2014-04 |
Orally active microtubule-targeting agent, MPT0B271, for the treatment of human non-small cell lung cancer, alone and in combination with erlotinib
|
Tsai, A-C; Wang, C-Y; Liou, J-P; Pai, H-C; Hsiao, C-J; Chang, J-Y; Wang, J-C; Teng, C-M; Pan, S-L |
朝陽科技大學 |
2014-02 |
An Integrative Process Model of Users’ Health Information Search Behavior and Information Adoption
|
劉熒潔;Liou, J-P |
臺北醫學大學 |
2014 |
Preclinical anti-arthritic study and pharmacokinetic properties of a potent histone deacetylase inhibitor MPT0G009
|
Hsieh, I-N;Liou, J-P;Lee, H-Y;Lai, M-J;Li, Y-H;Yang, C-R |
國立臺灣大學 |
2014 |
Orally active microtubule-targeting agent, MPT0B271, for the treatment of human non-small cell lung cancer, alone and in combination with erlotinib
|
Tsai, A-C; Wang, C-Y; Liou, J-P; Pai, H-C; Hsiao, C-J; Chang, J-Y; Wang, J-C; Teng, C-M; Pan, S-L; 鄧哲明 |
國立臺灣大學 |
2014 |
Preclinical anti-arthritic study and pharmacokinetic properties of a potent histone deacetylase inhibitor MPT0G009
|
Hsieh, I-N; Liou, J-P; Lee, H-Y; Lai, M-J; Li, Y-H; Yang, C-R; 楊家榮 |
臺北醫學大學 |
2013 |
Histone deacetylase inhibition improved cardiac functions with direct antifibrotic activity in heart failure
|
Kao, Y. H.;Liou, J. P.;Chung, Chung C. C.;Lien, G. S.;Kuo, C. C.;Chen, S. A.;Chen, Y. J. |
臺北醫學大學 |
2013 |
Histone deacetylase inhibition improved cardiac functions with direct antifibrotic activity in heart failure
|
Kao, Y.H.;Liou, J.P.;Chung, C.C.;Lien, G.S.;Kuo, C.C.;Chen, S.A.;Chen, Y.J. |
國立臺灣大學 |
2004-12 |
Total synthesis of lycoramine: an intramolecular Heck reaction to the galanthamine skeleton.
|
Liang, P. -H.; Liou, J. -P.; Hsin, L. -W.; Cheng, C. -Y. |
中國醫藥大學 |
2004-07 |
A novel bis-benzylidenecyclopentanone derivative, BPR0Y007, inducing a rapid caspase activation involving upregulation of Fas (CD95/APO-1) and wild-type p53 in human oral epidermoid carcinoma cells.
|
莊聲宏(Shin-Hun Juang); (Pan, W.-Y); (Kuo, C.-C.); (Liou, J.-P); (Hung, Y.-M); (Chen, L.-T.); (Hsieh, H.-P.); (Chang, J.-Y. *)* |
中國醫藥大學 |
2004-05-01 |
A novel bis-benzylidenecyclopentanone derivative, BPR0Y007, inducing a rapid caspase activation involving upregulation of Fas (CD95/APO-1) and wild-type p53 in human oral epidermoid carcinoma cells
|
莊聲宏(Shin-Hun Juang); (Pan, W.-Y.); (Kuo, C.-C.); (Liou, J.-P.); (Hung, Y.-M.); (Hung, Y.-M.); (Chang, J.-Y.)* |
中國醫藥大學 |
2004-03-27 |
A novel bis-benzylidenecyclopentanone derivative, BPR0Y007, induces a rapid caspases activation involving upregulation of Fas (CD95/APO-1) and wild-type p53 in human oral epidermoid carcinoma cells.
|
莊聲宏(Shin-Hun Juang); (Pan, W.-Y.); (Kuo, C.-C.); (Liou, J.-P.); (Chen, L.-T.); (Hsieh, H.-P.); (Chang, J.-Y.)* |