Isolation of Biologically Active Compounds from the Flower Petals of Carthamus tinctorius L.

홍화(Carthamus tinctorius L.)로부터 활성물질의 분리

  • Kim, Yung-Hee (Kyung Hee University, College of Industry, Department of Life Science & Resources, Institute of Life Sciences & Resources) ;
  • Ahn, Eun-Mi (Kyung Hee University, College of Industry, Department of Life Science & Resources, Institute of Life Sciences & Resources) ;
  • Bang, Myun-Ho (Kyung Hee University, College of Industry, Department of Life Science & Resources, Institute of Life Sciences & Resources) ;
  • Nam, Ji-Youn (Korea Research Institute of Bioscience and Biotechnology, KIST) ;
  • Kwon, Byung-Mok (Korea Research Institute of Bioscience and Biotechnology, KIST) ;
  • Baek, Nam-In (Kyung Hee University, College of Industry, Department of Life Science & Resources, Institute of Life Sciences & Resources)
  • 김융희 (경희대학교 산업대학 생명자원과학부 및 생명자원과학연구원) ;
  • 안은미 (경희대학교 산업대학 생명자원과학부 및 생명자원과학연구원) ;
  • 방면호 (경희대학교 산업대학 생명자원과학부 및 생명자원과학연구원) ;
  • 남지연 (한국과학기술연구원 생명공학연구소) ;
  • 권병목 (한국과학기술연구원 생명공학연구소) ;
  • 백남인 (경희대학교 산업대학 생명자원과학부 및 생명자원과학연구원)
  • Published : 1998.04.30

Abstract

The MeOH extracts obtained from the flower petals of Carthamus tinctorius were solvent-fractionated with EtOAc, n-BuOH, and $H_2O$, successively. From the n-BuOH extract 2 flavonoid compounds were isolated through the repeated silica gel column chromatographies. From not only the results of physico-chemical data including HMBC but also the adaptation of acid hydrolysis, the chemical structures of the compounds were determined as $3-O-[{\beta}-D-glucopyranosyl(1{\rightarrow}2)\;{\beta}-D-glucopyranosyl]\;kaempferol$ and $3-O-[{\alpha}-L-rhamnopyranosyl(1{\rightarrow}6)\;{\beta}-D-glucopyranosyl]\;kaempferol$. The compounds exhibited $IC_{50}$ values in Grab2-Shc activity to be 43 and $47{\mu}g/ml$, respectively.

홍화 MeOH 추출물의 n-BuOH 분획으로부터 silica gel column chromatography를 반복하여 2종의 flavonoid 배당체를 분리, 정제하였다. 화합문의 화학구조를 HMBC를 포함한 NMR, MS, IR과 같은 기기분석 결과와 산가수분해반응을 이용하여 결정, 각각 $3-O-[{\beta}-D-glucopyranosyl(1{\rightarrow}2)\;{\beta}-D-glucopyranosyl]\;kaempferol$$3-O-[{\alpha}-L-rhamnopyranosyl(1{\rightarrow}6)\;{\beta}-D-glucopyranosyl]\;kaempferol$로 동정하였다. 각 화합물은 Grb2-Shc 결합저해활성$(IC_{50}:43,\;47\;{\mu}g/ml)$을 나타내었다.

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