Synthesis and anti-cancer activity of 5,6,7-substituted 2-fluorophenyl-4-quinolone derivatives
碩士 === 中國醫藥大學 === 藥物化學研究所碩士班 === 97 === In our continuing work aimed at the discovery and development of novel anticancer agents, 2-(2-fluorophenyl)-6,7-(methylenedioxy)-4-quinolone was identified as a promising anticancer drug candidate. Encouraged by the preliminary results, 2-(2-fluorophenyl...
Main Authors: | Meng-Tung Tsai, 蔡孟東 |
---|---|
Other Authors: | 郭盛助 |
Format: | Others |
Language: | zh-TW |
Published: |
2009
|
Online Access: | http://ndltd.ncl.edu.tw/handle/31891195394357855010 |
Similar Items
-
Synthesis and Structure Activity Relationship of 5,6,7-trimethoxyindoles and 5,6,7-trimethoxy-2-oxoindoles as anticancer agents
by: Ling-Yin Chang, et al.
Published: (2009) -
The synthesis of 5,6,7- and 7,7-fused azepine systems
by: Hayes, R.
Published: (1987) -
Synthesis and anti-cancer activity of 6-diethylaminomethyl-2-(2-fluorophenyl)-4-quinolone and 2-(3-diethylaminomethylphenyl)-4-quinolone analogues
by: Ching-Che Huang, et al.
Published: (2007) -
Inhibitory Effects of 5,6,7-Trihydroxyflavones on Tyrosinase
by: Jun Kawabata, et al.
Published: (2007-01-01) -
Auto-oxidation of 5,6,7 ,8-tetrahydroneopterin
by: Arai Toshiyuki, et al.
Published: (1998-02-01)