3-Aminonaphtostyril誘導体の合成とその抗菌作用

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概要

• 論文の詳細を見る

• 3-Aminonaphthostyril derivatives were synthesized from mercurinaphthalic anhydride, an acenaphthene derivative, by utilizing the reactivity of its carbon-mercury bond. Although an ergot-like physiological activity was anticipated in 3-aminonaphthostyril derivatives, there was no such activity. However, antibacterial tests revealed that the derivative having p-aminobenzenesulfonyl group substituted in the 3-amino group had an inhibitory action on tubercle bacilli.

• 公益社団法人日本薬学会の論文
• 1978-11-25

著者

• 鷹觜 照男

  Faculty Of Pharmaceutical Sciences Toko University

• 鷹觜 照男

  東邦大学薬学部

関連論文

• Syntheses of Diphenic Anhydride-Mercury Compounds and Their Reaction with Nucleophilic Reagents
• 3-Aminonaphtostyril誘導体の合成とその抗菌作用
• 無水ナフタル酸水銀化物の合成および求核試薬との反応

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