• Title/Summary/Keyword: Melandrin

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Synthesis of Melandrin (Melandrin의 합성)

  • 문정술;이강노;임중기;우원식
    • YAKHAK HOEJI
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    • v.35 no.4
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    • pp.332-334
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    • 1991
  • The synthesis of melandrin has been accomplished in good yield by the reaction of 5-tosyloxyanthranilic acid ethyl ester with p-acetoxybenzoyl chloride, followed by removal of protecting groups with methanolic ammonia.

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Synthesis of Melandrin Derivatives (Melandrin 유도체의 합성)

  • Lim, Jung-Ki;Woo, Won-Sick;Lee, Kang-Ro;Ma, Eun-Sook
    • YAKHAK HOEJI
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    • v.38 no.3
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    • pp.281-285
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    • 1994
  • Melandrin was isolated from the Melandrium firmum(Caryophyllaceae), its structure was N-(p-hydroxybenzoyl)-5-hydroxyanthranilic acid. Fourteen melandrin derivatives(I-XIV) were synthesized and according to MME calculation by the computer, optimized three dimensional structure of compounds was obtained. The space orientation of compounds was cis-form as a indomethacin.

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Analgesic and Hypothermic Activities of Melandrin

  • Lee, Eun-Bang;Cheon, Seon-Ah;Lee, Young-Soon;Chung, Ha-Sook;Woo, Won-Sick
    • Archives of Pharmacal Research
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    • v.18 no.1
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    • pp.38-40
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    • 1995
  • melandrin exhibited an analgesic activity as assessed by inhibition of writhing syndromein mice and by pressure method of inflamed paws of arts and inflamed tails of mmice, and showed a hypothermic effect. However, no anti-inflammatory activity was shown.

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Analgesic, Anti-inflammatory and Antiviral Effects of Melandrin Derivatives (Melandrin유도체의 진통 소염 및 항바이러스 효과)

  • Lim, Jung-Ki;Lee, Eun-Bang;Woo, Won-Sik;Lee, Kang-Ro;Lee, Yeong-Sun;Ma, Eun-Sook
    • YAKHAK HOEJI
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    • v.38 no.3
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    • pp.345-350
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    • 1994
  • Fourteen melandrin derivatives(I-XIV) were investigated on analgesic, anti-inflammatory and antiviral activities . Compound I [N-(p-hydroxybenzoyl)-5-hydroxyanthranilic acid methvl ester], Xll [N-(2-phenoxypropionyl)-5-hydroxy anthranilic acid propyl ester and XIV [N-(2-phenoxypropionyl)-5-hydroxyanthranilic acid exhibited analgesic activity in tail pressure and Randall-Selitto method. But no anti-inflammatory activity was shown. Compound I exhibited weak antiviral activity on Herpes simplex virus type I F strain by virus-induced cytopathic effect(CPE) assay and it's selectivity index(Sl) was 8.17.

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Synthesis of N-Substituted 5-Hydroxyanthranilic Acid (N-치환 5-Hydroxyanthranilic acid의 합성)

  • 문정술;이강노;임중기;우원식;박상우
    • YAKHAK HOEJI
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    • v.37 no.3
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    • pp.243-246
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    • 1993
  • Six N-substituted-5-hydroxyanthranilic acids were synthesized by the coupling reaction of 5-tosyloxyanthranilic acid ethyl ester with corresponding acid chlorides. The structure of the obtained compounds was proved by NMR and IR. These compounds did not inhibit the growth of micro-organisms while suppressed HSV-1 replication in vero cell at 100 $\mu\textrm{g}$/ml.

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