Studies on the Benzo[f]indole-4,9-dione Derivatives

碩士 === 高雄醫學大學 === 醫藥暨應用化學研究所 === 97 === This study confers mainly how to synthesize the feature of benzo[f]indole-4,9-dione dervatives with the structure of planar tricyclic ring. We can confer the series of compounds whether they have the activity of anti-cancer and anti-bacterial by way of modifyi...

Full description

Bibliographic Details
Main Authors: You-Ren Chen, 陳宥任
Other Authors: Cherng-Chyi Tzeng
Format: Others
Language:zh-TW
Published: 2009
Online Access:http://ndltd.ncl.edu.tw/handle/97141688364732054034
id ndltd-TW-097KMC05537017
record_format oai_dc
spelling ndltd-TW-097KMC055370172015-11-13T04:09:13Z http://ndltd.ncl.edu.tw/handle/97141688364732054034 Studies on the Benzo[f]indole-4,9-dione Derivatives 苯并[f]吲哚-4,9-二酮類化合物之研究 You-Ren Chen 陳宥任 碩士 高雄醫學大學 醫藥暨應用化學研究所 97 This study confers mainly how to synthesize the feature of benzo[f]indole-4,9-dione dervatives with the structure of planar tricyclic ring. We can confer the series of compounds whether they have the activity of anti-cancer and anti-bacterial by way of modifying the C-4 carbonyl group and the N-1 position. The primitive result of indicated that 1-vinyl-1H-benzo[f]indole-4,9-dione (22q) shows the most potent activity of anti-cancer. When the C-4 position of the ring was derivatized with alkoxyimino or procainamido group, the activity of anti-cancer was enhanced. The result of anti-bacteria evaluation shows that 4-(4-(dimethylamino)- butoxyimino)-1-phenethyl-1H-benzo[f]indol-9(4H)-one (34g) possesses an obvious effect for inhibit the production of biofilm. Cherng-Chyi Tzeng 曾誠齊 2009 學位論文 ; thesis 112 zh-TW
collection NDLTD
language zh-TW
format Others
sources NDLTD
description 碩士 === 高雄醫學大學 === 醫藥暨應用化學研究所 === 97 === This study confers mainly how to synthesize the feature of benzo[f]indole-4,9-dione dervatives with the structure of planar tricyclic ring. We can confer the series of compounds whether they have the activity of anti-cancer and anti-bacterial by way of modifying the C-4 carbonyl group and the N-1 position. The primitive result of indicated that 1-vinyl-1H-benzo[f]indole-4,9-dione (22q) shows the most potent activity of anti-cancer. When the C-4 position of the ring was derivatized with alkoxyimino or procainamido group, the activity of anti-cancer was enhanced. The result of anti-bacteria evaluation shows that 4-(4-(dimethylamino)- butoxyimino)-1-phenethyl-1H-benzo[f]indol-9(4H)-one (34g) possesses an obvious effect for inhibit the production of biofilm.
author2 Cherng-Chyi Tzeng
author_facet Cherng-Chyi Tzeng
You-Ren Chen
陳宥任
author You-Ren Chen
陳宥任
spellingShingle You-Ren Chen
陳宥任
Studies on the Benzo[f]indole-4,9-dione Derivatives
author_sort You-Ren Chen
title Studies on the Benzo[f]indole-4,9-dione Derivatives
title_short Studies on the Benzo[f]indole-4,9-dione Derivatives
title_full Studies on the Benzo[f]indole-4,9-dione Derivatives
title_fullStr Studies on the Benzo[f]indole-4,9-dione Derivatives
title_full_unstemmed Studies on the Benzo[f]indole-4,9-dione Derivatives
title_sort studies on the benzo[f]indole-4,9-dione derivatives
publishDate 2009
url http://ndltd.ncl.edu.tw/handle/97141688364732054034
work_keys_str_mv AT yourenchen studiesonthebenzofindole49dionederivatives
AT chényòurèn studiesonthebenzofindole49dionederivatives
AT yourenchen běnbìngfyǐnduǒ49èrtónglèihuàhéwùzhīyánjiū
AT chényòurèn běnbìngfyǐnduǒ49èrtónglèihuàhéwùzhīyánjiū
_version_ 1718129211391082496