• 제목/요약/키워드: 9,12-(9E, 12E)-Octadecadienoic acid

검색결과 8건 처리시간 0.024초

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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황기(Astragalus membranaceus Bunge) 뿌리의 성분 연구 (II) (A Study on the Constituents from the Roots of Astragalus membranaceus (II))

  • 김진숙;김정숙
    • 생약학회지
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    • 제28권2호
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    • pp.75-79
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    • 1997
  • Two compounds were isolated from roots of Astragalus membranaceus Bunge. On the basis of chemical spectro scopic evidence, they were identified as Formononetin (compound E) and Linoleic acid (9Z,12Z-Octadecadienoic acid) (compound F). Linoleic acid (9Z,12Z-Octadecadienoic acid) was reported the first time from the genus Astragalus.

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Induction of Growth Hormone by the Roots of Astragalus membranaceus in Pituitary Cell Culture

  • Kim, Chung-Sook;Ha, Hye-Kyung;Kim, Jin-Sook;Kim, Yun-Tai;Kwon, Sun-Chang;Park, Sie-Won
    • Archives of Pharmacal Research
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    • 제26권1호
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    • pp.34-39
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    • 2003
  • The traditional Asian medicinal herb, roots of Astragalus (A.) membranaceus (Leguminosae), is used for many purposes, some of which are purported to stimulate the release of growth hormone in vivo. Extracts of A. membranaceus were tested to determine whether they stimulate the release of growth hormone in rat pituitary cell culture. A. membranaceus was extracted sequentially with 80% ethanol (fraction A), n-hexane (fraction B); the test compound from the herbal extraction was isolated using silica gel column chromatography and was identified with spectral data. Test compound was also extracted by traditional boiling water methods. Induction of growth hormone in pituitary cell culture was conducted with isolated compounds and extracted fractions of A. Radix (dried roots of A. membranaceus). The fraction A was not active in the rat pituitary cell culture, but the fraction B derived from the ethanol fraction stimulated the release of growth hormone in culture. Six compounds from fraction B (1-6) were isolated and identified previously. The compounds 1,2-benzendicarboxylic acid diisononylester (1), $\beta$-sitosterol (2), and 3-Ο-$\beta$-D-galactopyranosyl-$\beta$-sitosterol (5) did not induce growth hormone release in the culture. Formononetin (3), 9Z, 12Z-octadecadienoic acid (4), stigmast-4-en-6$\beta$-o1-3-one (6) and 98-E, a mixture of 1'-9, 12-octadecadienoic acid (Z,Z)-2',3'-dihydroxy-propylester (7) and 1'-hexadecanoic acid-2',3'-dihydroxy-propylester (8) stimulated the release of growth hormone in the rat pituitary cell culture significantly compared to the control. In conclusions, four compounds isolated from extracts of A. Radix induced growth hormone release in the rat pituitary cell culture. The 98-E isolate was the most active inducer of growth hormone release.

진달래꽃 탄화수소류의 곡자에 의한 분해 (The Degradation of hydrocarbons in Petal of Azalea by Gokja)

  • 홍태희
    • 한국식품영양학회지
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    • 제12권4호
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    • pp.415-420
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    • 1999
  • Petal of Azalea(Rhododendron mucronulatum Turcz) was incubated with Gokja at 3$0^{\circ}C$ for seven days and the essential oil components of petal of Azalea before and after incubated were analyzed using a GC/MSD. Ten or more essential oil components including n-heneicosane n-tricosane n-tetreacosane n-pentacosane n-heptacosane n-nonacosane and n-hentriacontane were identified from the petal of Azal-ea before incubated while oxygen-containng compounds including (E)-heptenal 2-ethoxy-1 -hexanol n-hexadecanoic acid methyl ester 9, 12-octadecadienoic acid methyl ester 9,12,15-octadecatrienoic acid methyl ester, n-octadecanoic acid methyl ester n-eicosanoic acid methyl ester and 9-docosaenoic acid methyl ester as well as n-alkanes such as n-tricosane that n-pentacosane were identified from the petal of Azalea after incubated. These results suggest that n-alkanes in petal of Azalea might be degraded and some oxygen-containing compounds such as aldehyde, esters and /or acids might be produced when pet-al of Azalea is incubated with Gokja.

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생지황(生地黃) 증류 추출 약침액과 초임계 유체 추출물의 성분 연구(硏究) (The Study on the Composition of Rehmanniae Radix Extracts by Supercritical Carbon Dioxide Extraction and by Hydrodistillation Extraction)

  • 허종원;육태한
    • Journal of Acupuncture Research
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    • 제28권2호
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    • pp.89-95
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    • 2011
  • Objectives : The purpose of this study was to investigate the composition of Rehmannia glutinosa's essential oils with Rehmanniae Radix herbal acupuncture Methods : I obtained the essential oils of Rehmannia Radix by hydrodistillation extraction method and supercritical fluid extraction(SFE) method, and then I analyzed those by GC/MS(gas chromatography/mass spectrum). Results : 1. With GC(gas chromatography) and GC/MS(gas chromatography/mass spectrum) analysis. I identified 9 compounds in the Rehmanniae Radix's essential oil obtained through the SFE method. The main compounds were as follows : Hexachloroethane(2.24%), N-Butyl-benzenesulfonamide(2.05%), hexadecanoic acid(1.93%), hexadecanoic acid, ethyl ester(3.49%), 9,12-Octadecadienoic acid(z,z)(2.70%), (9E)-9-Octadecenoic acid(6.14%), ethyl linoleate(4.43%), ethyl oleate(5.80%). 2. I failed to get Rehmanniae Radix's essential oil obtained through the hydrodistillation method. 3. With GC(gas chromatography) and GC/MS(gas chromatography/mass spectrum) analysis. I identified 4 compounds in the Rehmanniae Radix's essential oil obtained through the hydrodistillation method. The main compounds were as follows : Ethylbis(trimethylsilyl)amine(1.04%), 2-(Trimethylsiloxy)benzoic methyl ester(2.65%), Hexadecanoic acid trimethylsilyl ester(12.61%), octadecanoic acid, trimethylsilyl ester(6.28%). Conclusions : The substances by hydrodistillation method may not perfectly match with the substances by supercritical fluid extraction(SFE) method in essential oils extracted form Rehmanniae Radix. But, the main substances was assumed Hexadecanoic acid and octadecanoic acid.

Bioactive Compound Produced by Endophytic Fungi Isolated From Pelargonium sidoides Against Selected Bacteria of Clinical Importance

  • Manganyi, Madira Coutlyne;Tchatchouang, Christ-Donald K.;Regnier, Thierry;Bezuidenhout, Cornelius Carlos;Ateba, Collins Njie
    • Mycobiology
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    • 제47권3호
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    • pp.335-339
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    • 2019
  • Endophytic fungi have the ability to live inside the host plant tissues without causing neither symptoms of diseases/or harm. Opportunistic infections are accountable for majority of the outbreaks, thereby putting a burden on the health system. To investigate and characterize the bioactive compounds for the control of bacteria of clinical importance, extracts from endophytic fungi were isolated from indigenous South African medicinal plants. Extracts from endophytic fungi were isolated from 133 fungal strains and screened against Gram positive and negative bacteria namely Bacillus cereus, Escherichia coli, Enterococcus faecium, and E. gallinarum using disk diffusion. Furthermore, gas chromatography-mass spectrometry was performed to identify the bioactive compounds. Sixteen out of one hundred and thirty-three (12%) fungi extracts exhibited antibacterial properties against some of the selected bacteria. E. coli was found to be the most susceptible in contrast to E. faecium and E. gallinarum which were the most resistant. The isolate MHE 68, identified as Alternaria sp. displayed the greater spectrum of antibacterial activities by controlling selected clinical bacteria strains including resistant E. faecium and E. gallinarum. The chemical analysis of the extract from MHE 68 indicated that linoleic acid (9,12-octadecadienoic acid (Z,Z)) and cyclodecasiloxane could be accountable for the antibacterial activity. This is the first study conducted on the secondary metabolites produced by endophytic fungal strains isolated from the Pelargonium sidoides DC. possessing antibacterial properties.

해양미세조류 에탄올 추출물의 항균활성에 관한 연구 (Antibacterial activity of ethanol extracts from marine micro-algae)

  • 김윤정;하상철;김대욱;신일식
    • 한국식품과학회지
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    • 제49권4호
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    • pp.390-395
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    • 2017
  • Mixed A, Chlorella vulgaris, Nannochloropsis oculata, Chaetoceros calcitrans 등 4종류의 미세조류로부터 99.9% 에탄올로 추출한 성분의 항균활성을 검증하기 위해 그람음성세균 2종(E. coli, S. Typhimurium)과 그람양성세균 2종(S. aureus, B. cereus)에 대하여 paper disk diffusion assay, MIC, MBC를 측정하였다. 4종류의 미세조류 추출물은 공시균주에 대하여 0.62-1.66 mg/mL의 MIC를 나타내었으며, C. vulgaris 추출물이 4종의 공시균주에 대한 MIC가 0.62 mg/mL로 가장 강한 항균활성을 나타내었으며, MBC 또한 C. vulgaris 에탄올 추출물이 E. coli에 대해 2.50 mg/mL, S. aureus, B. cereus와 S. Typhimurium에 대해서는 4.16-5.00 mg/mL로 가장 강한 항균활성을 나타내었다. 항균활성이 가장 강한 C. vulgaris 에탄올 추출물의 성분을 분석한 결과, 함량이 가장 많은 성분은 9,12-octadecadienoic acid (linoelaidic acid, peak 5, 7)로 38.8%이었으며, 그 다음이 2-Hexadecen-1-o1, 3,7,11,15-tetramethyl (phytol, peak 2,6)로 30.0%이었다. Octadecadienoic acid는 일명 linoelaidic acid로 탄소수 18개의 고도불포화지방산이며, 두 번째로 함량이 많은 Phytol은 클로로필을 구성하는 불포화 제1급 알코올의 일종으로서(엽록소의 구성 성분) 병원성 대장균 및 황색포도상구균에 항균활성을 나타낸다는 보고로 볼 때, 이 2가지 성분이 항균활성의 주성분인 것으로 사료된다.

Induction of Nrf2/ARE-mediated cytoprotective genes by red ginseng oil through ASK1-MKK4/7-JNK and p38 MAPK signaling pathways in HepG2 cells

  • Bak, Min Ji;Truong, Van-Long;Ko, Se-Yeon;Nguyen, Xuan Ngan Giang;Jun, Mira;Hong, Soon-Gi;Lee, Jong-Won;Jeong, Woo-Sik
    • Journal of Ginseng Research
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    • 제40권4호
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    • pp.423-430
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    • 2016
  • Background: The induction of cellular defensive genes such as phase II detoxifying and antioxidant enzymes is a highly effective strategy for protection against carcinogenesis as well as slowing cancer development. Transcription factor Nrf2 (nuclear factor E2-related factor 2) is responsible for activation of phase II enzymes induced by natural chemopreventive compounds. Methods: Red ginseng oil (RGO) was extracted using a supercritical $CO_2$ extraction system and chemical profile of RGO was investigated by GC/MS. Effects of RGO on regulation of the Nrf2/antioxidant response element (ARE) pathway were determined by ARE-luciferase assay, western blotting, and confocal microscopy. Results: The predominant components of RGO were 9,12-octadecadienoic acid (31.48%), bicyclo[10.1.0] tridec-1-ene (22.54%), and 22,23-dihydrostigmasterol (16.90%). RGO treatment significantly increased nuclear translocation of Nrf2 as well as ARE reporter gene activity, leading to upregulation of heme oxygenase-1 and NAD(P)H:quinone oxidoreductase 1. Phosphorylation of the upstream kinases such as apoptosis signal-regulating kinase (ASK)1, mitogen-activated protein kinase (MAPK) kinase (MKK)4/7, c-Jun N-terminal kinase (JNK), and p38 MAPK were enhanced by treatment with RGO. In addition, RGO-mediated Nrf2 expression and nuclear translocation was attenuated by JNK inhibitor SP600125 and p38 MAPK inhibitor SB202190. Conclusion: RGO could be used as a potential chemopreventive agent, possibly by induction of Nrf2/ARE-mediated phase II enzymes via ASK1-MKK4/7-JNK and p38 MAPK signaling pathways.