• 제목/요약/키워드: squalene synthase inhibitor

검색결과 5건 처리시간 0.017초

울금(Curcuma longa)으로부터 분리한 squalene synthase 저해물질의 특성 (Characterization of Squalene Synthase Inhibitor Isolated from Curcuma longa)

  • 최성원;양재성;이한승;김동섭;배동훈;유주현
    • 한국식품과학회지
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    • 제35권2호
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    • pp.297-301
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    • 2003
  • 동맥경화증과 같은 심혈관 질환을 야기시키는 주요 위험요인인 혈중 콜레스테롤의 수준을 낮추기 위하여 콜레스테롤 생합성 과정의 속도조절단계 효소의 하나인 squalene synthase의 활성을 저해하는 물질을 분리 정제하여, 물질의 이화학적 특성과 생물학적 특성을 검토하였다. Squalene synthase 저해물질은 acetone extraction, ethyl acetate extraction, silica gel column chromatography, sephadex LH-20 column chromatography, 결정화 등을 이용하여 분리 정제하여 YUF-01을 얻었다. 기기분석을 통하여 구조분석을 행한 결과 YUF-01은 분자량 368, 분자식 $C_{20}H_{21}O_6$으로 분석되었으며 243과 421 nm 에서 UV-VIS 흡광을 나타내었고 $^{13}C$ NMR spectrum과 $^1H$ NMR spectrum을 검토하였을 때 aromatic ketone 구조인 curcuminoid 계통의 curcumin과 일치하였다. Squalene synthase에 대한 curcumin의 $IC_{50}$ 값은 $100{\mu}M$이었으며, non-competitive inhibitor로 작용하였다.

Isolation and Structural Determination of Squalene Synthase Inhibitor from Prunus mume Fruit

  • Choi, Sung-Won;Hur, Nam-Yoon;Ahn, Soon-Cheol;Kim, Dong-Seob;Lee, Jae-Kwon;Kim, Dae-Ok;Park, Seung-Kook;Kim, Byun-Yong;Baik, Moo-Yeol
    • Journal of Microbiology and Biotechnology
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    • 제17권12호
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    • pp.1970-1975
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    • 2007
  • Squalene synthase plays an important role in the cholesterol biosynthetic pathway. Inhibiting this enzyme in hypercholesterolemia can lower not only plasma cholesterol but also plasma triglyceride levels. A squalene synthase inhibitor was screened from Prunus mume fruit, and then purified via sequential processes of ethanol extraction, HP-20 column chromatography, ethyl acetate extraction, silica gel column chromatography, and crystallization. The squalene synthase inhibitor was identified as chlorogenic acid with a molecular mass of 354 Da and a molecular formula of $C_{16}H_{18}O_9$ based on UV spectrophotometry, $^1H$ and $^{13}C$ NMRs, and mass spectrometry. Chlorogenic acid inhibited the squalene synthase of pig liver with an $IC_{50}$ level of 100 nM. Since chlorogenic acid was an effective inhibitor against the squalene synthase of an animal source, it may be a potential therapeutic agent for hypercholesterolemia.

Hypocholestrolemic Effect of CJ90002 in Hamsters: A Potent Inhibitor for Squalene Synthase from Paeonia moutan

  • Park, Jong-Koo;Cho, Hi-Jae;Lim, Yoon-Gho;Cho, Youl-Hee;Lee, Chul-Hoon
    • Journal of Microbiology and Biotechnology
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    • 제12권2호
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    • pp.222-227
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    • 2002
  • Squalene synthase catalyzes the reductive dimerization of two molecules of farnesyl diphosphate to form squalene at the final branch point of the cholesterol biosynthetic pathway. Due to the unique position of this enzyme in the pathway, its inhibitors may have advantages as antihypercholesterolemic agents. Therefore, selective inhibitors of squalene synthase do not prevent the formation of the essential branch products of the isoprene pathway, such as dolichol, coenzyme-Q, and prenylated proteins, as might be expected for inhibitors of enzymes earlier in the pathway; for example, lovastatin and mevalotin. The current study reports that CJ90002, a pentagalloylglucose isolated from Paeonia moutan SIM (Paeoniaceae), which is an important Chinese crude drug used in many traditional prescriptions, was a potent inhibitor of rat microsomal squalene synthase, and also a potent inhibitor of cholesterol biosynthesis in vitro. In addition, the intraperitoneal and oral administration of CJ90002 had a significant lowering effect on plasma cholesterol levels in hamsters.

Purification and Identification of Squalene Synthase Inhibitor Isolated from Fermented Soybean Paste

  • Choi, Sung-Won;Kim, Dong-Seob;Hur, Nam-Youn;Park, Cheon-Seok;Baik, Moo-Yeol
    • Food Science and Biotechnology
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    • 제14권1호
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    • pp.89-93
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    • 2005
  • Squalene synthase (SQS) inhibitors were screened from various plants and food extracts. Effective SQS inhibitor was purified from fermented soybean paste using ethanol extraction, HP-20 column chromatography, ethyl acetate extraction, silica gel column chromatography, and crystallization. Through UV spectrometry, $^1H$ NMR, $^{13}C$ NMR, and mass spectrometry, SQS inhibitor was identified as daidzein with molecular mass of 254 and molecular formula of $C_{15}H_{10}O_4$. Daidzein showed $IC_{50}$ value of 50 nmol/L against SQS, confirming its potential as therapeutic agent for hypercholesterolemia.

녹차의 squalene synthase 저해효과 (Inhibitory Effects of Green Tea against Squalene Synthase)

  • 최성원;허남윤;이한승;백무열;안순철;이정규
    • 생명과학회지
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    • 제18권2호
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    • pp.273-278
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    • 2008
  • 콜레스테롤 생합성 과정에 있어서 속도조절 단계 효소의 하나인 squalene synthase에 대한 저해물질의 탐색을 목적으로, 30종의 다양한 천연물을 대상으로 squalene synthase에 대해 저해효과를 검토한 결과 녹차추출물에서 비교적 저해활성이 높고 재현성이 있게 저해효과를 나타내는 것으로 확인되었다. 녹차에 함유되어 있는 squalene synaase에 대한 저해물질의 용매추출성을 검토한 결과 ethyl acetate와 n-butanol 층에 저해물질이 많이 함유되어 있는 것으로 확인되었으며 저해물질은 녹차의 polyphenol 화합물인 catechin에 의한 것으로 추정되었다. Catechin 표준용액의 각 농도에 따른 squalene synthase 저해작용을 살펴 본 결과, (-)-epigallocatechin gallate, (-)-epicatechin gallate, (-)-epigauocatechin, (-)-epicatechin, (+)-catechin의 순으로 저해활성이 강한 것으로 나타났으며 가장 강한 저해활성을 나타내는 (-)-epigallocatechin gallate의 $IC_{50}$값은 $90{\mu}M$이었다.