Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Kung-Cheng Liu"'
Autor:
Kung-Cheng Liu, 柳公政
95
Part I： It has been reported that the expression of sialic acid is directly correlated with metastatic potential of cancer cells. In patients’ tumor cells, there is great increase in activities of sialytransferases (ST). We tried to desig
Part I： It has been reported that the expression of sialic acid is directly correlated with metastatic potential of cancer cells. In patients’ tumor cells, there is great increase in activities of sialytransferases (ST). We tried to desig
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/27397897325976128394
Publikováno v:
The Journal of Organic Chemistry. 81:10832-10844
An efficient and trans-diastereoselective Rh(I)-catalyzed 1,4-conjugate addition reaction of alkenylboronic acids and a homochiral (R)-4-silyloxycyclopentenone useful for the synthesis of derivatives of prostaglandins E and F is described for the fir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12b59a9db44864acac73612e4b0c0f25
https://doi.org/10.1021/acs.joc.6b01913
https://doi.org/10.1021/acs.joc.6b01913
Autor:
Kung-Cheng Liu, Jim-Min Fang, Jia-Tsrong Jan, Ting-Jen R. Cheng, Shi-Yun Wang, Shi-Ting Yang, Yih-Shyun E. Cheng, Chi-Huey Wong
Publikováno v:
Journal of Medicinal Chemistry. 55:8493-8501
Influenza therapy with a single targeted compound is often limited in efficacy due to the rapidly developed drug resistance. Moreover, the uncontrolled virus-induced cytokines could cause the high mortality of human infected by H5N1 avian influenza v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5aad8a919e0c15c96594224e6adc337d
https://doi.org/10.1021/jm3009844
https://doi.org/10.1021/jm3009844
Publikováno v:
Bioorganic & Medicinal Chemistry. 19:4796-4802
Zanamivir (ZA) is a potent anti-influenza drug, but it cannot be administrated orally because of the hydrophilic carboxylate and guanidinium groups. Guanidino-oseltamivir (GO) is another effective neuraminidase inhibitor with polar guanidinium group
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c40378ce1493596e0a89776c6b400652
https://doi.org/10.1016/j.bmc.2011.06.080
https://doi.org/10.1016/j.bmc.2011.06.080
Autor:
Hui Chuan Chang, Wing See Lam, Kung-Cheng Liu, Sachin S. Shivatare, Ya Ching Jen, Yu-Ting Hsu, Wen-Shan Li, Shu-Chuan Jao, Chie-Hong Wang
Publikováno v:
Organic letters. 12(1)
A new type of competitive human GST inhibitors has been developed via the bioisostere and structure activity profile strategies; we report their discovery, preparation, inhibitory activity, and synergetic effect in combination with chemotherapy drugs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbafcea1c19d8723a19884b98eb7b2fb
https://pubmed.ncbi.nlm.nih.gov/19961147
https://pubmed.ncbi.nlm.nih.gov/19961147
Publikováno v:
ChemInform. 37
We report two synthetic systems, Cu(Bpy)2+ and Cu(Phen)2+, for catalytic hydrogenation of steroidal haloalkenes in the presence of hydrazine and air. Thesestudies demonstrated that the selective hydrogenation is faster for the 1,10‐phenanthroline
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16347c3bb23574a932759779552d8854
https://doi.org/10.1002/chin.200634191
https://doi.org/10.1002/chin.200634191
Autor:
Jin-Fong Syu, Yun-Ting Wang, Kung-Cheng Liu, Ping-Yu Wu, Henschke, Julian P., Hsyueh-Liang Wu
Publikováno v:
Journal of Organic Chemistry; 11/18/2016, Vol. 81 Issue 22, p10832-10844, 13p
Autor:
Wen-Shan Li, Wing See Lam, Kung-Cheng Liu, Chie-Hong Wang, Hui Chuan Chang, Ya Ching Jen, Yu-Ting Hsu, Sachin S. Shivatare, Shu-Chuan Jao
Publikováno v:
Organic Letters; Jan2010, Vol. 12 Issue 1, p20-23, 4p