• Title/Summary/Keyword: phenanthrene alkaloid

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Studies on the Cytotoxic Constituent of Saururus chinensis$(L_{OUR.})\;B_{AILL.}$ (삼백초의 세포독성 성분연구)

  • Park, Si-Kyung;Oh, Gab-Jin;Bae, Choon-Il;Kim, Hyun-Jong;Han, Wan-Sik;Chung, Sun-Gan;Cho, Eui-Whan
    • YAKHAK HOEJI
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    • v.41 no.6
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    • pp.704-708
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    • 1997
  • In our search for bioactive natural products with antitumor activity, we have valuated various extracts of Saururi Herba (Saururaceae), which has been used in traditional medici ne for edema, beriberi, jaundice, turbid urine, carbuncle and furuncle. The hexane extract of the aerial part of this plant was found to show a potent cytotoxicity against several kinds of cultured human solid tumor cell lines (AGS, A549, HCT15, SKOV3, HEP-3B) in vitro. Using cytotoxicity-guided chromatographic separation of the hexane extract, cytotoxic constituent: 10-aminomethyl-3-hydroxy-4-methoxyphenanthrene-carboxylic acid lactam, was isolated and structurally identified by physico-chemical properties and spectroscopic evidences.

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Efficient Total Synthesis of (-)-Antofine by Using (R)-(E)-4-(tributylstannanyl)but-3- en-2-ol as a Chiral building block

  • Lee, Eun-Jung;Lee, Tae-Ho;Lee, Jaek-Wang;Kim, Sang-Hee
    • Proceedings of the PSK Conference
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    • 2003.10b
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    • pp.182.3-183
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    • 2003
  • (-)-Antofine is phenanthroindolizidine alkaloid being isolated from Cynanchum vincetoxicum. It has powerful cytotoxicity toward drug-sensitive KB-3-1 and multidrug resistant KB-V1 cancer cell line. We have successfully accomplished stereoselective total synthesis by using palladium catalyzed Stille coupling of l0-bromomethyl-2,3 ,6-trimethoxy-phenanthrene and (R)-(E)-4-(tributylstannanyl)but-3-en-2-o1, Overmann rearrangement of imidate, and RCM(ring-closing metathesis) for construction of pyrrolidine.

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