Meisenheimer Rearrangement of Azetopyridoindoles. VIII. Synthesis and Antiviral Activities of 12-Carbaeudistomin Analogs
スポンサーリンク
概要
- 論文の詳細を見る
Eudistomins, isolated from the colonial tunicate Eudistoma olivaceum, have been a synthetic target due to their strong antiviral activity against Herpes simplesx virus (HSV-1) and activities against certain types of tumors in vivo. In order to examine the structure-activity relationship of eudistomins, 12-carbaeudistomin analogs were synthesized and their activities against influenza A and B virus, HSV-1,HSV-2 and human cytomegalovirus were investigated. Among them, racemic 6-methoxy-12-carbaeudistomin showed similar activity to (-)-debromoeudistomin K, synthesized as a control compound.
- 公益社団法人日本薬学会の論文
- 1996-05-15
著者
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大石 宏文
Osaka University of Pharmaceutical Sciences
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OHISHI Hirofumi
Osaka University of Pharmaceutical Sciences
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Ohishi H
Osaka University Of Pharmaceutical Sciences
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Kimura Tetsuya
Osaka University Of Pharmaceutical Sciences
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Suzutani Tatsuo
Department Of Microbiology Fukushima Medical University
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Azuma Masanobu
Asahikawa Medical College Department Of Microbiology
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Kurihara T
Osaka University Of Pharmaceutical Sciences
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Ohishi H
Osaka Univ. Pharmaceutical Sci. Osaka Jpn
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米田 龍司
Agroscience Research Laboratories Sankyo Co. Ltd.
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HARUSAWA Shinya
Osaka University of Pharmaceutical Sciences
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SAKAMOTO Yasuhiko
Osaka University of Pharmaceutical Sciences
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YONEDA Ryuji
Osaka University of Pharmaceutical Sciences
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KURIHARA Takushi
Osaka University of Pharmaceutical Sciences
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SUZUTANI Tatsuo
Asahikawa Medical College, Department of Microbiology
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Sakamoto Y
Alfresa Pharma Co.
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