산오리나무의 세포독성 성분연구

Studies on the Cytotoxic Constituent of Alnus hirsuta$(S_{PACH})\;R_{UPR}$

  • 배춘일 (삼진제약(주) 중앙연구소) ;
  • 공재명 (삼진제약(주) 중앙연구소) ;
  • 오정완 (삼진제약(주) 중앙연구소) ;
  • 김현종 (삼진제약(주) 중앙연구소) ;
  • 오갑진 (삼진제약(주) 중앙연구소) ;
  • 박시경 (삼진제약(주) 중앙연구소) ;
  • 정순간 (삼진제약(주) 중앙연구소) ;
  • 조의환 (삼진제약(주) 중앙연구소)
  • Bae, Choon-Il (Central Research Institute, Samjin Pharmaceutical Co., LTD.) ;
  • Gong, Jae-Myung (Central Research Institute, Samjin Pharmaceutical Co., LTD.) ;
  • Oh, Jung-Wan (Central Research Institute, Samjin Pharmaceutical Co., LTD.) ;
  • Kim, Hyun-Jong (Central Research Institute, Samjin Pharmaceutical Co., LTD.) ;
  • Oh, Gab-Jin (Central Research Institute, Samjin Pharmaceutical Co., LTD.) ;
  • Park, Si-Kyung (Central Research Institute, Samjin Pharmaceutical Co., LTD.) ;
  • Chung, Sun-Gan (Central Research Institute, Samjin Pharmaceutical Co., LTD.) ;
  • Cho, Eui-Hwan (Central Research Institute, Samjin Pharmaceutical Co., LTD.)
  • 발행 : 1997.10.01

초록

To find out antitumor active principles from natural resources, we have evaluated various extracts from the leaves of Alnus hirsuta (Betulaceae). The ethylacetate extract of this plant was found to show a significant cytotoxicity against several kinds of cultured human solid tumor cell lines (AGS, A5 49, HCT15, SKOV3, HEP3B) in vitro. Using cytotoxicity-guided chromatographic purification of the ethylacetate extract, cytotoxic constituent:1,7-bis-(4-hydroxyphenyl)-5-(${\beta}$-D-glucopyranosyloxy)-3-heptanone, was isolated and structurally identified by physico-chemical properties and spectroscopic evidences.

키워드

참고문헌

  1. 대한 식물 도감 이창복
  2. 한국의 자원식물(Ⅰ) 김태정
  3. 원색 천연 약물대사전(하권) 김재길
  4. 新編 中藥大辭典(中) 新文豊出判公司
  5. J. Natl. Cancer Inst. v.82 New colorimetric cytotoxicity assay for anticancer-drug screening. Skehan, P.;Storeng, R.;Scudiero, D. A.;Monks, A.;McMahon, J.;Vistica, D.;Warren, J. T.;Bokesch, H.;Kenney, S.;Boyd. M. R.
  6. J. Natl. Cancer Inst. v.83 Feasibility of a high-flux anticancer drug screen using adiverse panel of cultured human tumor cell line. Monks, A.;Scudiero, D.;Skehan, P.;Shoemaker, R.;Paull, K.;Vistica, D.;Hose, C.;Langley, L.;Cronise, P.;Vaigro-Wolff, A.;Gray-Goodrich, M.;Campbell, H.;Mayo, J;boyd, M. R.
  7. Phytochemistry v.32 Arylbutanoid and diarylheptanoid glycosides from inner bark of Betula pendula. Smite, E.;Lundgren, L. N.;Anderson, R.
  8. Phytochemistry v.20 Biarylheptanoids and other constituents from wood of Alnus japonica. Nomura, M.;Tokoroyama, T.;Kubota, T.
  9. Bull. Chem. Soc. Jpn. v.56 An X-ray crystallographic study on the absolute configuration of dihydroxyashabushiketol and the solvent-dependence of its optical rotation. Suga, T.;Ohta, S.;Aoki, T.;Hirata, T.
  10. J. Chem. Soc. Perkin Trans. v.1 The structures of four diarylheptanoid glycosides from the female flowers of Alnus serrulatoides. Ohta, S.;Aoki, T.;Hirata, T.;Suga, T.
  11. Betula platyphylla Skatch. var. japonica Hara. Mokuzai Gakkaishi v.19 Isolation of platyphyllonol, a new diaryheptanoid from the green bark of Shirakanba. Terazawa, M.;Koga, T.;Okuyama, H.;Miyake, M.
  12. Bull. College Exp. For Cooege Agric. Hokkaido Univ. JPN. v.31 Sasaya, T.;Izumiyama, K.;Phenolic compounds from the wood of Keyama-hannoki Alnus hirsuta Turcz.(Betulaceae).
  13. J. Am. Chem. Soc. v.100 Determination of the absolute configurationof a secondary hydroxy group in a chiral secondary alcohol using glycosidation shifts in carbon 13 nuclear magnetic resonance spectroscopy. Seo, S.;Tomita, Y.;Tori, K.;Yoshimura, Y.
  14. Bull. Chem. Soc. Jpn. v.58 Absolute configuration of platyphylloside and (-)-centrolobol. Ohata, S.;Koyama, M.;Aoki, T.;Suga, T.
  15. Mokuzai Gakkaishi v.30 Phenolic compounds in living tissue of woods Ⅲ. Terazawa, M.;Koga, T.;Okuyama, H.;Miyake, M.
  16. Japan pharmaceutical information center Drugs in Japan (ethical drugs) Yakugyo Jiho Co.