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Sedative activity and its active components of zizyphi fructus

  • Han, Byung-Hoon;Park, Myung-Hwan
    • Archives of Pharmacal Research
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    • v.10 no.4
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    • pp.208-211
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    • 1987
  • Sedative activity of Zizyphi fructus was evaluated by potentiation of hexobarbital-induced hypnosis test and its active principles have been characterized as nornuciferine and lysicamine. A new cyclopeptide alkaloid, daechucyclopeptide-1 was isolated together with zizyphusine.

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Flavonoids from the Rhizomes of Belamcanda chinensis

  • Chung, Ha-Sook;Woo, Won-Sick
    • Archives of Pharmacal Research
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    • v.14 no.4
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    • pp.357-358
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    • 1991
  • Two flavonoids were isolated from the rhizomes of Belamcanda chinensis and identified as kanzakiflavove-2 and 2R:3R-dihydrokaempferol-7-methylether, respectively.

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Novel Bromolactonization Using N-bromophthalimide

  • Cook, Chae-Ho;Kang, Eung-Ku
    • Archives of Pharmacal Research
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    • v.4 no.2
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    • pp.137-139
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    • 1981
  • Reaction of olefinic acids with N-bromophthalimide in dry N, N-dimethylf-ormamide at room temperature gives bromolactones in good yields.

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Sapogenins from albizzia julibrissin

  • Kang, Sam-Sik;Woo, Won-Sick
    • Archives of Pharmacal Research
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    • v.6 no.1
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    • pp.25-28
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    • 1983
  • From the stem bark of Albizzia julibrissin (Leguminosae) two known sapogenins, acacigenin B, and machaerinic acid lactone, were isolated and identified by chemical and spectral data. It is the second time that the former was isolate dform the plant sources.

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Phytochemical study on melandrium firmum

  • Woo, Won-Sicka;Choi, Jae-Sue;Chang, Hye-Soon
    • Archives of Pharmacal Research
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    • v.8 no.3
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    • pp.133-137
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    • 1985
  • The aglycones of saponins isolated from Melandrium firmum were identified as gypsogenin, gypsogenic acid and quillaic acid.

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The absolute configuration of ketoprofen

  • Kim, Jin-Woong;Jew, Sang-Sup;Cho, Youn-Sang;Cook, Chae-Ho
    • Archives of Pharmacal Research
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    • v.10 no.1
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    • pp.25-28
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    • 1987
  • (+)-Ketoprofen was obtained form resolution with (S) (+)-2-amino-1-butanol and its absolute configuration was determined to be (S) by chemical correlation with (S) (+)-ethyl hydratropate using Beckmann rearrangement as a key step.

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