Synthesis and Antiviral Activities of Some 4,4'-Dihydroxytriphenylmethanes
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概要
- 論文の詳細を見る
4,4'-Dihydroxytriphenylmethanes were synthesized using Bronsted acid or Lewis acid in yields of 24-86% as target compounds for developing antiviral agents. Most of the 4,4'-dihydroxytriphenylmethanes showed significant activity against herpes simplex virus type 1 (anti-HSV-1 activity) in a plaque reduction assay. Higher cyto-toxicity was observed generally in halogenated 4,4'-dihydroxytriphenylmethanes (2a-d) than in non-halogenated derivatives. The non-halogenated derivative, 4,4',4"-trihydroxy-3"-methoxytriphenylmethane (3), showed remarkable antiviral activity with an EC_<50> value of 1.8 μg/ml.
- 公益社団法人日本薬学会の論文
- 2003-11-01
著者
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Mibu N
Faculty Of Pharmaceutical Sciences Fukuoka University
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YOKOMIZO Kazumi
Faculty of Medical and Pharmaceutical Sciences, Kumamoto University
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UYEDA Masaru
Faculty of Medical and Pharmaceutical Sciences, Kumamoto University
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Uyeda Masaru
Dep. Of Nutrition Sci. Facultiy Of Living Sci. Shokei Univ.
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Uyeda Masaru
Laboratory Of Pharmaceutical Microbiology Faculty Of Medical And Pharmaceutical Sciences Kumamoto Un
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Uyeda Masaru
Shokei University
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Yokomizo K
Kumamoto Univ. Kumamoto Jpn
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Udayama M
Kumamoto Univ. Kumamoto Jpn
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Mibu Nobuko
Faculty Of Pharmaceutical Sciences Fukuoka University
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Yokomizo Kazumi
Laboratory Of Pharmaceutical Microbiology Faculty Of Medical And Pharmaceutical Sciences Kumamoto Un
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Yokomizo Kazumi
Faculty Of Pharmaceutical Sciences Kumamoto University
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SUMOTO Kunihiro
Faculty of Pharmaceutical Sciences, Fukuoka University
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Udayama Manabu
Faculty Of Pharmaceutical Sciences Kumamoto University
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Uyeda Masaru
Department Of Pharmaceutical Microbiology Faculty Of Medical And Pharmaceutical Sciences Kumamoto Un
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Sumoto K
Faculty Of Pharmaceutical Sciences Fukuoka University
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Sumoto Kunihiro
Fukuoka Univ. Fukuoka Jpn
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Sumoto Kunihiro
Faculty Of Pharmaceutical Sciences Fukuoka University
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Sumoto Kunihiro
Faculty of Pharmaceutical Science, Fukuoka University
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