Rhinovirus Inhibition by Bufadienolides
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概要
- 論文の詳細を見る
An evaluation of thirty-four bufadienolides and two related cardenolides against a series of rhinoviruses in vitro has been completed. Most of the bufadienolides were found to display some inhibitory activity. Scillarenin and 3-O-[N-(tert-butoxycarbonyl)hydrazido]succinylbufalin were found to be the most active with chemotherapeutic indices of 32 and 16,respectively. In general, the 14β-hydroxy-bufadienolides showed the strongest antiviral activity, and were found more toxic than the corresponding 14β, 15β-epoxy-bufadienolides. Introduction of a 16β-hydroxy or 16β-acetoxy substituent into the 14β, 15β-epoxybufadienolides enhanced their antiviral activity. Substituents at the 3β-, 5β-, and 19-positions appeared to affect only the level of toxicity.
- 公益社団法人日本薬学会の論文
- 1988-01-25
著者
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釜野 徳明
Cencer Reseach Institute And Department Of Chemistry Arizona State University
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佐藤 統夫
Cencer Reseach Institute And Department Of Chemistry Arizona State University
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Pettit George
Cencer Reseach Institute And Department Of Chemistry Arizona State University
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仲吉 洋
Cencer Reseach Institute and Department of Chemistry, Arizona State University
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SMITH CECIL
Cencer Reseach Institute and Department of Chemistry, Arizona State University
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Smith Cecil
Cencer Reseach Institute And Department Of Chemistry Arizona State University
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仲吉 洋
Cencer Reseach Institute And Department Of Chemistry Arizona State University
関連論文
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- Studies on Topical Antiinflammatory Corticosteroids. I. Syntheses and Vasoconstrictive Activities of 11β, 17α, 21-Trihydroxy-6α-methyl-1,4-pregnadiene-3,20-dione 17-Ester and 17,21-Diester Derivatives
- Rhinovirus Inhibition by Bufadienolides
- Bufadienolides. XX. 14β-Chloro-bufadienolides
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