Zobrazeno 1 - 10
of 45
pro vyhledávání: '"陳基旺"'
Publikováno v:
Chinese Journal of Rice Science; 2022, Vol. 36 Issue 1, p55-64, 10p
Publikováno v:
Journal of Southern Agriculture; Apr2020, Vol. 51 Issue 4, p790-797, 8p
Autor:
Ji-Wang Chen, 陳基旺
93
Fourty-one compounds isolated from the Allium sativum L. were identified as trans-sulfuric acid allyl ester-3-allysulfanyl-allyl ester, allicidin-A, allicidin-B, bis-2-propenyl disulfide, bis-2-propenyl trisulfide, bis-2-propenyl tetrasulfide
Fourty-one compounds isolated from the Allium sativum L. were identified as trans-sulfuric acid allyl ester-3-allysulfanyl-allyl ester, allicidin-A, allicidin-B, bis-2-propenyl disulfide, bis-2-propenyl trisulfide, bis-2-propenyl tetrasulfide
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/74183355972137610120
Autor:
Ravindra Ramesh Deore, 迪歐
100
The chronic hepatitis C virus (HCV) infection progressively leads to major liver disorders such as cirrhosis, end stage liver disease and hepatocellular carcinoma. While almost 3% of world’s population is infected by HCV, the lone treatmen
The chronic hepatitis C virus (HCV) infection progressively leads to major liver disorders such as cirrhosis, end stage liver disease and hepatocellular carcinoma. While almost 3% of world’s population is infected by HCV, the lone treatmen
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/06201858758158777764
Autor:
Hsueh-Yun Lee, 李學耘
98
An attempt to develop potent agents to arrest cell cycle, E7010 (6) was chosen as the lead compound. Based on conformational restriction approach, to constrain the secondary amine linkage between pyridine and benzene in E7010 was proposed. Ac
An attempt to develop potent agents to arrest cell cycle, E7010 (6) was chosen as the lead compound. Based on conformational restriction approach, to constrain the secondary amine linkage between pyridine and benzene in E7010 was proposed. Ac
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/52140611308061909449
Autor:
Chiung-Hua Huang, 黃瓊嬅
98
While chronic inflammation is widely believed to be a predisposing factor for cancer, the exact mechanisms linking these conditions have remained elusive. CX9051, a benzo[1.3.2]dithiazolium ylide 1,1-dioxide derivative identified as a COX-2 a
While chronic inflammation is widely believed to be a predisposing factor for cancer, the exact mechanisms linking these conditions have remained elusive. CX9051, a benzo[1.3.2]dithiazolium ylide 1,1-dioxide derivative identified as a COX-2 a
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/71675463904357369026
Autor:
Fei-Chiao Kuo, 郭斐荍
97
This thesis is aimed to majorly design a series of isoquinolinone derivatives as neurite outgrowth modulators and perhaps also as dipeptidyl peptidase 4 (DPP 4) inhibitor. The synthesis of isoquinolinone derivatives were started from commerci
This thesis is aimed to majorly design a series of isoquinolinone derivatives as neurite outgrowth modulators and perhaps also as dipeptidyl peptidase 4 (DPP 4) inhibitor. The synthesis of isoquinolinone derivatives were started from commerci
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/43086513688695573901
Autor:
Bettie Der-Yuin Jea, 賈德韻
95
Hepatitis C virus (HCV) has become a serious etiological agent worldwide. HCV sets up a persistent infection in 70-80% of cases, and can lead to cirrhosis or hepatoma. Currently available interferon-based treatments show limited efficacy. The
Hepatitis C virus (HCV) has become a serious etiological agent worldwide. HCV sets up a persistent infection in 70-80% of cases, and can lead to cirrhosis or hepatoma. Currently available interferon-based treatments show limited efficacy. The
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/89449597891846577591
Autor:
Yin-Ling Wei, 魏吟玲
93
The aim of this thesis is to design and synthesize quinoline derivatives as potential cytotoxic agents. Two series of target compounds, 3-phenylquinolines (7-10) and 2-phenylquinolines (11-14, 17 and 18), were prepared and evaluated for their
The aim of this thesis is to design and synthesize quinoline derivatives as potential cytotoxic agents. Two series of target compounds, 3-phenylquinolines (7-10) and 2-phenylquinolines (11-14, 17 and 18), were prepared and evaluated for their
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/60126835714289198157
Autor:
廖培因
90
This thesis is aimed in (i) the design and synthesis of 6-oxo-indolo[1,2-b]benzo[1,2,4]thiadiazine 12,12-dioxide derivatives, analogues of tryptanthrin, as potential novel anticancer drugs; (ii) tryptanthrin containing polyamine side chain, b
This thesis is aimed in (i) the design and synthesis of 6-oxo-indolo[1,2-b]benzo[1,2,4]thiadiazine 12,12-dioxide derivatives, analogues of tryptanthrin, as potential novel anticancer drugs; (ii) tryptanthrin containing polyamine side chain, b
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/42443269891015872005