| 臺大學術典藏 |
2021-06-02T05:43:44Z |
Ardisianone, a natural benzoquinone, efficiently induces apoptosis in human hormone-refractory prostate cancers through mitochondrial damage stress and survivin downregulation
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Yu C.-C.; Wu P.-J.; Hsu J.-L.; Ho Y.-F.; Hsu L.-C.; Chang Y.-J.; Chang H.-S.; Chen I.-S.; JIH-HWA GUH |
| 臺大學術典藏 |
2021-06-02T05:43:44Z |
Antroquinonol, a natural ubiquinone derivative, induces a cross talk between apoptosis, autophagy and senescence in human pancreatic carcinoma cells
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Yu C.-C.; Chiang P.-C.; Lu P.-H.; Kuo M.-T.; Wen W.-C.; Chen P.; JIH-HWA GUH |
| 臺大學術典藏 |
2021-06-02T05:43:44Z |
Structure-based design, synthesis and evaluation of novel anthra[1,2-d]imidazole-6,11-dione derivatives as telomerase inhibitors and potential for cancer polypharmacology
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Chen C.-L.; Chang D.-M.; Chen T.-C.; Lee C.-C.; Hsieh H.-H.; Huang F.-C.; Huang K.-F.; JIH-HWA GUH; Lin J.-J.; Huang H.-S. |
| 臺大學術典藏 |
2021-06-02T05:43:43Z |
Total synthesis of 14,21-diepi-squamocin-K
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Liu C.-W.; Yeh T.-C.; Chen C.-H.; Yu C.-C.; Chen C.-S.; Hou D.-R.; JIH-HWA GUH |
| 臺大學術典藏 |
2021-06-02T05:43:43Z |
Erratum: Anti-angiogenic effects and mechanism of prazosin (The Prostate (2011) 71 (976-984))
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Liao C.-H.; JIH-HWA GUH; Chueh S.-C.; Yu H.-J. |
| 臺大學術典藏 |
2021-06-02T05:43:43Z |
Synthesis of a chlorogenin glycoside library using an orthogonal protecting group strategy
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Wang Y.-H.; Yeh H.-W.; Wang H.-W.; Yu C.-C.; JIH-HWA GUH; Liu D.-Z.; Liang P.-H. |
| 臺大學術典藏 |
2021-06-02T05:43:42Z |
Terfenadine induces anti-proliferative and apoptotic activities in human hormone-refractory prostate cancer through histamine receptor-independent Mcl-1 cleavage and Bak up-regulation
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Wang W.-T.; Chen Y.-H.; Hsu J.-L.; Leu W.-J.; Yu C.-C.; Chan S.-H.; Ho Y.-F.; Hsu L.-C.; JIH-HWA GUH |
| 臺大學術典藏 |
2021-06-02T05:43:42Z |
Design, synthesis and antiproliferative evaluation of fluorenone analogs with DNA topoisomerase i inhibitory properties
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Lee C.-C.; Chang D.-M.; Huang K.-F.; Chen C.-L.; Chen T.-C.; Lo Y.; JIH-HWA GUH; Huang H.-S. |
| 臺大學術典藏 |
2021-06-02T05:43:42Z |
Reevesioside F induces potent and efficient anti-proliferative and apoptotic activities through Na+/K+-ATPase α3 subunit-involved mitochondrial stress and amplification of caspase cascades
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Chan S.-H.; Leu W.-J.; Hsu L.-C.; Chang H.-S.; Hwang T.-L.; Chen I.-S.; Chen C.-S.; JIH-HWA GUH |
| 臺大學術典藏 |
2021-06-02T05:43:42Z |
A novel hydroxysuberamide derivative potentiates MG132-mediated anticancer activity against human hormone refractory prostate cancers - The role of histone deacetylase and endoplasmic reticulum stress
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Chen Y.-C.; Huang W.-J.; Hsu J.-L.; Yu C.-C.; Wang W.-T.; JIH-HWA GUH |
| 臺大學術典藏 |
2021-06-02T05:43:41Z |
Moniliformediquinone induces in vitro and in vivo antitumor activity through glutathione involved DNA damage response and mitochondrial stress in human hormone refractory prostate cancer
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Hsu J.-L.; Lee Y.-J.; Leu W.-J.; Dong Y.-S.; Pan S.-L.; Uang B.-J.; JIH-HWA GUH |
| 臺大學術典藏 |
2021-06-02T05:43:40Z |
Reevesioside A, a cardenolide glycoside, induces anticancer activity against human hormone-refractory prostate cancers through suppression of c-myc expression and induction of G1 arrest of the cell cycle
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Leu W.-J.; Chang H.-S.; Chan S.-H.; Hsu J.-L.; Yu C.-C.; Hsu L.-C.; Chen I.-S.; JIH-HWA GUH |
| 臺大學術典藏 |
2021-06-02T05:43:40Z |
A unique amidoanthraquinone derivative displays antiproliferative activity against human hormone-refractory metastatic prostate cancers through activation of LKB1-AMPK-mTOR signaling pathway
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Hsu J.-L.; Liu S.-P.; Lee C.-C.; Hsu L.-C.; Ho Y.-F.; Huang H.-S.; JIH-HWA GUH |
| 臺大學術典藏 |
2021-06-02T05:43:39Z |
Cephalochromin induces G0/G1 cell cycle arrest and apoptosis in A549 human non-small-cell lung cancer cells by inflicting mitochondrial disruption
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Hsiao C.-J.; Hsiao G.; Chen W.-L.; Wang S.-W.; Chiang C.-P.; Liu L.-Y.; JIH-HWA GUH; Lee T.-H.; Chung C.-L. |
| 臺大學術典藏 |
2021-06-02T05:43:39Z |
Synthesis and anti-cancer activity of a glycosyl library of \varvec{N} N -acetylglucosamine-bearing oleanolic acid
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Zeng Y.-B.; Hsiao H.-M.; Chan S.-H.; Wang Y.-H.; Lin Y.-Y.; Kuo Y.-H.; JIH-HWA GUH; Liang P.-H. |
| 臺大學術典藏 |
2021-06-02T05:43:38Z |
A general synthetic strategy and the anti-proliferation properties on prostate cancer cell lines for natural phenylethanoid glycosides
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Mulani S.K.; JIH-HWA GUH; Mong K.-K.T. |
| 臺大學術典藏 |
2021-06-02T05:43:38Z |
Calanquinone A induces anti-glioblastoma activity through glutathione-involved DNA damage and AMPK activation
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Liu F.-L.; Hsu J.-L.; Lee Y.-J.; Dong Y.-S.; Kung F.-L.; Chen C.-S.; JIH-HWA GUH |
| 臺大學術典藏 |
2021-06-02T05:43:37Z |
The Akt inhibitor MK-2206 enhances the cytotoxicity of paclitaxel (Taxol) and cisplatin in ovarian cancer cells
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Lin Y.-H.; Chen B.Y.-H.; Lai W.-T.; Wu S.-F.; JIH-HWA GUH; Cheng A.-L.; Hsu L.-C. |
| 臺大學術典藏 |
2021-06-02T05:43:37Z |
A novel small molecule hybrid of vorinostat and DACA displays anticancer activity against human hormone-refractory metastatic prostate cancer through dual inhibition of histone deacetylase and topoisomerase i
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Yu C.-C.; Pan S.-L.; Chao S.-W.; Liu S.-P.; Hsu J.-L.; Yang Y.-C.; Li T.-K.; Huang W.-J.; JIH-HWA GUH |
| 臺大學術典藏 |
2021-06-02T05:43:37Z |
Ring fusion strategy for the synthesis of anthra[2,3-d ]oxazole-2-thione-5,10-dione homologues as DNA topoisomerase inhibitors and as antitumor agents
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Chen C.-L.; Liu F.-L.; Lee C.-C.; Chen T.-C.; Chang W.-W.; JIH-HWA GUH; Ahmed Ali A.A.; Chang D.-M.; Huang H.-S. |
| 臺大學術典藏 |
2021-06-02T05:43:36Z |
Structural studies and anticancer activity of a novel class of β-peptides
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Kudryavtsev K.V.; Yu C.-C.; Ivantcova P.M.; Polshakov V.I.; Churakov A.V.; Br?se S.; Zefirov N.S.; JIH-HWA GUH |
| 臺大學術典藏 |
2021-06-02T05:43:36Z |
Epi-reevesioside F inhibits Na+/K+-ATPase, causing cytosolic acidification, Bak activation and apoptosis in glioblastoma
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Hsu J.-L.; Liu F.-L.; Hsu L.-C.; Chang H.-S.; Leu W.-J.; Yu C.-C.; Chang W.-L.; Chen I.-S.; Kung F.-L.; JIH-HWA GUH |
| 臺大學術典藏 |
2021-06-02T05:43:35Z |
Cytotoxic protobassic acid glycosides from Planchonella obovata leaf
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Chen H.-Y.; JIH-HWA GUH; Chan S.-H.; Lee S.-S. |
| 臺大學術典藏 |
2021-06-02T05:43:35Z |
Repurposing of nitroxoline as a potential anticancer agent against human prostate cancer - A crucial role on AMPK/mTOR signaling pathway and the interplay with Chk2 activation
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Chang W.-L.;Hsu L.-C.;Leu W.-J.;Chen C.-S.;Jih-Hwa Guh; Chang W.-L.; Hsu L.-C.; Leu W.-J.; Chen C.-S.; JIH-HWA GUH |
| 臺大學術典藏 |
2021-06-02T05:43:35Z |
Repurposing of phentolamine as a potential anticancer agent against human castration-resistant prostate cancer: A central role on microtubule stabilization and mitochondrial apoptosis pathway
|
Ho C.-H.; Hsu J.-L.; Liu S.-P.; Hsu L.-C.; Chang W.-L.; Chao C.C.-K.; JIH-HWA GUH |
