• 제목/요약/키워드: biologically active compound

검색결과 71건 처리시간 0.029초

한국산 인삼의 polyphenol 화합물의 생리활성 효과 (Identification of Biologically Active Compounds from Panax ginseng C. A. Meyer)

  • 최희진;장운빈;안봉전;최청
    • 한국식품과학회지
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    • 제34권3호
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    • pp.493-497
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    • 2002
  • 한국산 인삼 5년근을 60% acetone으로 추출하여 Sepadex LH-20 gel column chromatography, MCI-CHP 20 gel column chromatography, Bondapak $C_{18}$, column chromatography을 이용하여 TLC와 HPLC로 순도를 검증한 후 3 종의 polyphenol 화합물을 분리하였다. Compound I과 II는 Sepadex LH-20 gel column chromatography에서 증류수상에서 용출되었고 compound Ⅲ는 40% methanol 상에서 용출됨을 보아 compound II와 compound III는 흡착성이 강한 polyphenol 화합물이라 추정되었다. 혈압강하에 관여하는 효소인 angiotensin converting enzyme(ACE)의 저해효과는 compound II가 157 ppm에서 31.86%로 3 가지 분획물 중 가장 우수하였으며 compound I과 III는 높은 활성을 보이지 않았다. 통풍예방에 관여하는 xanthine oxidase 저해효과는 compound I, II에서 666 ppm에서 100%저해효과를 나타내었으나 compound III는 저해효과가 낮았다. Melanin을 형성하는 tyrosinase 저해효과를 실함한 결과 compound III는 400 ppm에서 28.6%의 저해효과를 나타내었고 Compound I과 II의 저해효과는 낮았다.

Chemical Genomics with Natural Products

  • Jung, Hye-Jin;Ho, Jeong-Kwon
    • Journal of Microbiology and Biotechnology
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    • 제16권5호
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    • pp.651-660
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    • 2006
  • Natural products are a rich source of biologically active small molecules and a fertile area for lead discovery of new drugs [10, 52]. For instance, 5% of the 1,031 new chemical entities approved as drugs by the US Food and Drug Administration (FDA) were natural products between 1981 and 2002, and another 23% were natural product-derived molecules [53]. These molecules have evolved through millions of years of natural selection to interact with biomolecules in the cells or organisms and offer unrivaled chemical and structural diversity [14, 37]. Nonetheless, a large percentage of nature remains unexplored, in particular, in the marine and microbial environments. Therefore, natural products are still major valuable sources of innovative therapeutic agents for human diseases. However, even when a natural product is found to exhibit biological activity, the cellular target and mode of action of the compound are mostly mysterious. This is also true of many natural products that are currently under clinical trials or have already been approved as clinical drugs [11]. The lack of information on a definitive cellular target for a biologically active natural product prevents the rational design and development of more potent therapeutics. Therefore, there is a great need for new techniques to expedite the rapid identification and validation of cellular targets for biologically active natural products. Chemical genomics is a new integrated research engine toward functional studies of genome and drug discovery [40, 69]. The identification and validation of cellular receptors of biologically active small molecules is one of the key goals of the discipline. This eventually facilitates subsequent rational drug design, and provides valuable information on the receptors in cellular processes. Indeed, several biologically crucial proteins have already been identified as targets for natural products using chemical genomics approach (Table 1). Herein, the representative case studies of chemical genomics using natural products derived from microbes, marine sources, and plants will be introduced.

인삼품질에 있어 체형과 화합물과의 관계 (Shape and Compound Relationship in Ginseng Quality)

  • 박훈;이미경;조병구
    • 고려인삼학회:학술대회논문집
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    • 고려인삼학회 1988년도 학술대회지
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    • pp.133-138
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    • 1988
  • 인삼품질에 대한 전통개념을 역사적 경험, 전통적 품질관리방법 및 분석적 방법과 관련하여 조사하였다. 전통개념은 생명과 우주가 하나라는 한국의 기본사상에 근거한 것으로 보인다. 전통품질관리법에서 모양과 크기는 특정한 조직, 세포 및 세포내의 생리적 활성물질을 규정하기 때문에 전통품질관리법은 분석방법이 활성물질을 찾아가는 지도가 될 것이다. 전통법은 생물활성 물질간의 균형이 한 물질의 함량보다 중요하며 인체의 항샹성을 위한 활성물질의 작용양식도 여러 화합물, 여러 목표체계인 것으로 보인다. 인삼이 클 수록 중심부가 더 빨리 크고 중심부에는 질소화합물이 많기 때문에 전통법은 질소 화합물 특히, 수용성 단백질과 열안정단백질들이 활성물질의 균형에 있어 중요함을 강력히 시사한다. 생물활성물질의 균형은 삼속의 종간 사용방법의 차이와 의미있게 관계를 보인다.

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Aspergillus oryzae를 이용한 수삼으로부터 compound K로의 생물전환 (Biotransformation of Ginseng to Compound K by Aspergillus oryzae)

  • 김보혜;강주형;이선이;조효진;김영진;김윤진;안순철
    • 생명과학회지
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    • 제16권1호
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    • pp.136-140
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    • 2006
  • Ginseng was fermented by Aspergillus oryzae to search metabolites on the basis of increased biological activity and modified structure. From this research, two biotransformed compounds (WC2-2-1 and WC2-2-2) were detected and isolated through several chromatographic techniques. WC2-2-2 was confirmed to biologically active compound K by TLC, HPLC, and mass spectroscopy, while WC2-2-1 was going to be identified until now. In biological activity, both WG2-2-1 and WG2-2-2 exhibit the cytotoxicity on PC-3 cells, but WG2-2-2 was more active than WG2-2-1. It is supposed that WG2-2-1 is an intermediate metabolite transforming to final WG2-2-2, compound K.

Isolation and Partial Characterization of Phytotoxic Mycotoxins Produced by Sclerotinia sp., a Potential Bioherbicide for the Control of White Clover(Trifoliorum repens)

  • Hong, Yeon-Kyu;Lee, Bong-Choon;Jung, Won-Kwon;Bae, Soon-Do;Park, Sung-Tae;Uhm, Jae-Youl
    • The Plant Pathology Journal
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    • 제20권1호
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    • pp.52-57
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    • 2004
  • Sclerotinia sp. (isolate BWC98-105) causes stem blight and root rot in Leghum sp., and is presently being evaluated as a potential mycoherbicide for the control of Trifoliorium repens. Bioassays have shown that Sclerotinia sp. produces phytotoxic substance which is biologically active against T. repens. Two biologically active compounds, designated as compoundsI and II, were produced in vitro from the culture filtrate of BWC98-105 isolate Sclerotium sp. Compounds I and II were purified by means of liquid-liquid extraction and $C_{18}$ open column chromatography (300 ${\times}$ 30 mm, i.d). To determine the purity, the purified compounds were analyzed by RP-HPLC. The analytical RP-HPLC column was a TOSOH ODS-120T (150 ${\times}$ 4.6 mm i.d, Japan), of which the flow rate was set at 0.7 mL/min using the linear gradient solvent system initiated with 15 % methanol to 85 % methanol for 50 min with monitoring at 254 nm. Under these RP-HPLC conditions, compounds I and II eluted at 3.49 and 4.13 min, respectively. Compound II was found to be most potent and host specific. However, compound I had a unique antibiotic activity against phytopathogenic bacteria like bacterial leaf blight (Xanthomonas oryzae) on rice, where it played a less important role in producing toxicity on T. repens. No toxin activity was detected in the water fraction after partitioning with several organic solvents. However, toxin activity was detected in the ethyl acetate and butanol fractions. In the leaf bioassay using compound II, the disease first appeared within 4-5 h as water soaked rot, which subsequently developed into well-defined blight affecting the whole plant.

황정(黃精) 추출물의 화학구조 결정에 관한 연구(I) (Studies on Chemical Structure Determination of Polygonatum sibiricum Extracts(I))

  • 신동수;윤중호;박주희;권기락;안철진;주우홍;강진호;문병호
    • 생명과학회지
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    • 제9권2호
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    • pp.207-211
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    • 1999
  • 당뇨에 대한 황정의 약효가 알려지면서 황정의 생리활성 연구가 많이 진행되고 있다. 따라서 본 연구에서는 황정 추출물의 hexane층에서 생리활성 물질로 기대되는 새로운 화합물 I를 분리하고, 분리한 화합물의 화학적인 구조를 분광학적인 방법에 의하여 확인하였다. 1H-nmr, 13C-nmr, DEPT135, COSY, HMQC, HMBC 스펙트럼 및 MS 스펙트럼으로 확인하여 화합물 I의 구조가 9,12-(9E, 12E)-octadecadienoic acid 임을 알 수 있었다.

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황정(黃精) 추출물의 화학구조 결정에 관한 연구(II) (Studies on Chemical Structure Determination of Polygonatum sibiricum Extracts(II))

  • 신동수;김흥재;조수동;권기락;안철진;주우홍;강진호;문병호
    • 생명과학회지
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    • 제9권2호
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    • pp.212-215
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    • 1999
  • 본 연구에서는 황정(Polygonatum sibiricum) 추출물에서 생리활성 물질로 기대되는 새로운 화합물II를 분리하고, 분리한 화합물의 화학적인 구조를 분광학적인 방법에 의하여 확인하였다. IH-nmr, 13C-nmr, DEPT135, COSY, HMQC, HMBC 스펙트럼 및 MS 스펙트럼으로 확인하여 화합물II의 구조가 2-hydroxy-3-(9,12-(9E,12E)-octadecadienoyloxy) propanoic acid 임을 알 수 있었다.

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A New Antioxidant Polyphenolic Compound from Two Korean Brown Algae

  • Park, Soo-Hee;Kim, Eun-Sook;Choi, Byoung-Wook;Lee, Bong-Ho
    • 대한약학회:학술대회논문집
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    • 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.1
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    • pp.261.2-262
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    • 2003
  • In the course of our researches for biologically active compound from Korean algae, purification of the methanolic extracts of two brown algae (Sagassum Sagamianum and Ishige Okamurae) collected off Jeju Island afforded an antioxidant polyphenolic compound (1). The molecular formular of 1 was established as C$\sub$24/H$\sub$16/ O$\sub$13/ on the basis of the FAB mass and $\^$13/C NMR spectrum. (omitted)

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Coupling of ent-Cyclic Peroxide and Ircinol A, Two Biologically Active Natural Marine Products

  • Lim, Chi-Won;Kim, Yeun-Kye;Jang, Mi-Soon;Park, Jin-Il;Park, Hee-Yeun
    • Fisheries and Aquatic Sciences
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    • 제9권4호
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    • pp.175-178
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    • 2006
  • An acidic ent-cyclic peroxide was isolated from a sponge, Plakotis sp., and showed activity against leishmaniasis and pathogenic fungi. To improve the activity of this compound, we coupled the acidic ent-cyclic at the C1 position of ircinol A. Compound 3 exhibited significant activity against Leishmania mexican a and fungi with $IC_{50}$ values of 0.7 and $0.3-34{\mu}g/mL$, respectively. The yield of compound 3 was 98%.

식용 식물자원으로부터 활성물질의 탐색-IV. 달래(Allium monanthum Max.)로부터 Galactosyldiglyceridem의 분리 (Development of Biologically Active Compounds from Edible Plant Sources-IV. Isolation of Galactosyldiglyceride from the Allium monanthum Max.)

  • 백남인;안은미;김해영;박영두;장영진;김세영
    • 생명과학회지
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    • 제11권1호
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    • pp.93-96
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    • 2001
  • n-BuOH fraction obtained from MeOH extracts of Allium monanthum was applied to repeated silica gel column chromatographies to give a glycosylglyceride. The chemical structure of the compound was determined to be 1-O-linolenoyl-2-O-linolenoyl-3-O-$\beta$-D-galactopyranosyl-누-glycerol on the basis of NMR data and by the adaptation of chemical methods.

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