• 제목/요약/키워드: ${\beta}-sitosterol\

검색결과 352건 처리시간 0.025초

Isolation of ${\beta}-sitosterol$, Phytol and Zingerone $4-O-{\beta}-D-glucopyranoside$ from Chrysanthemum Boreale Makino

  • Kim, Dong-Hyun;Bang, Myun-Ho;Song, Myoung-Chong;Kim, Soon-Un;Chang, Young-Jin;Baek, Nam-In
    • 한국약용작물학회지
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    • 제13권5호
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    • pp.284-287
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    • 2005
  • The flowers of Chrysanthemum boreale Makino were extracted with 80% aqueous MeOH, and the concentrated extract was partitioned with n-hexane, EtOAc, n-BuOH and $H_2O$. Two compounds from the n-hexane fraction and one glucoside from the n-BuOH fraction were isolated through the repeated silica gel and ODS column chromatographies. From the result of physico-chemical data including NMR, MS and IR, the chemical structures of the compounds were determined as ${\beta}-sitosterol$ (1), phytol (2) and zingerone $4-O-{\beta}-D-glucopyranoside$ (3). Compounds 2 and 3 were isolated for the first time from this plant.

Pergularia tomentosa L.로부터의 카르데노리드와 ${\beta}$-시토스테롤 글루코사이드 (Cardenolides and ${\beta}$-Sitosterol Glucoside from Pergularia tomentosa L.)

  • Gohar, Ahmed A.;El-Olemy, M.M.;Abdel-Sattar, Essam;El-Said, M.;Niwa, M.
    • Natural Product Sciences
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    • 제6권3호
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    • pp.142-146
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    • 2000
  • 본 논문은 Pergularia tomentosa L.로부터의 카르데노리드와 ${\beta}$-시토스테롤 글루코사이드를 연구한 논문으로 주요내용으로는 Pergularia tomentosa L.의 지상부로부터 ${\beta}$-시토스테롤 글루코사이드와 함께 3가지 카데노이드, desglucouzarin, coroglaucigenin와 uzarigenin를 얻었다. 분리된 화합물은 IR, UV, $[{\alpha}]_D$, ID-, 2D-NMR 및 FAB-MS 실험을 포함하는 물리적 수단과 분광수단을 이용하여 동정되었다. 이전에 식물뿌리로부터 보고된 카르데노리드, ghalakinoside, calactin과 pergularoside가 지상부에서도 동정되었다는 내용이다.

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인삼성분이 초산발효에 미치는 영향에 관한 연구(제2보) (Studies on the Effect of Korean Ginseng Components on Acetic acid Fermentation. [II])

  • 남성희;유태종
    • Journal of Ginseng Research
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    • 제4권2호
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    • pp.133-145
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    • 1980
  • In order to find out the inhibitors of acetic acid fermentation in Korean ginseng (Panax Sin son C. A. Meyer), total aglycone, panaxadiol, panaxadiol, oleanolic acid and ${\beta}$ -sitosterol were added to the basal medium, respectively, and a surface culture was carried out at 30$^{\circ}C$. The results were as follows: 1 . Saponins lost their activity to inhibit the acetic acid fermentation by hydrolysis. 2 Panaxadiol inhibited slightly, and the degree of inhibition was about 1/300 of that of free saponins. 3. Panaxadiol and oleanolic acid inhibited silighly similar to total aglycone. 4. Acetic acid fermentation was stimulated at the early stage when ${\beta}$-sitosterol was added to the media below the level of 0.000815%. But the fermentation was inhibited when media contained it more than that media 5. An over-oxidation of acetic acid was observed when the media contained total aglycone. panaxadiol, panaxatriol, oleanolic acid and ${\beta}$-sitosterol, respectively, while the media which contained sucrose, ginseng extracts ginseng saponins was shown not to be over-oxidized.

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Identification of Metabolites of Phytosterols in Rat Feces Using GC/MS

  • Song, Yun-Seon;Jin, Chang-bae;Park, Eun-Hee
    • Archives of Pharmacal Research
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    • 제23권6호
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    • pp.599-604
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    • 2000
  • $\beta$-Sitosterol, campesterol and stigmasterol have been known to the phytosterols the most frequently found in plants. Metabolism of phytosterols was investigated using rat feces and liver microsomes. Feces were collected after phytosterols (a well characterized mixture of $\beta$-sitosterol 40%, campesterol 30% and dihydrobrasicasterol) were administered orally (0.5 ${g/kg$) to rats. Metabolites of phytosterols were identified using GC/MS. Three peaks were eluted at 12.47, 12.65, 12.87 min and had characteristic molecular ions m/z 428, 430, 432, respectively. Three fecal metabolites were identified as androstadienedione, androstenedione, and androstanedione. No metabolites could be detected in the rat liver microsomal reaction mixture. The results suggest that the metabolites of phytosterols in rat feces are formed by oxidation at 3- position, saturation at 5- and 6- position, and 17- side chain cleavage in the rat large intestine.

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옥수수 종실 및 속대의 Phytosterol 동정과 함량 변이 (Identification and Quantification of Phytosterols in Maize Kernel and Cob)

  • 김선림;김미정;정건호;이유영;손범영;김정태;이진석;배환희;고영삼;김상곤;백성범
    • 한국작물학회지
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    • 제63권2호
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    • pp.131-139
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    • 2018
  • 옥수수 종실(kernel)과 속대(cob)의 불검화물(ZML) 중 phytosterol의 조성과 함량의 변이를 구명하여 고품질 옥수수 신품종 육성 및 생리활성물질의 유용 소재화를 위한 기초자료로 활용하고자 본 연구를 실시하여 얻어진결과를 요약하면 다음과 같다. 1. 옥수수 종실과 속대의 포화지방산은 phytosterol 함량과 부의 상관관계의 경향이었고, 불포화지방산 중 stearic 및 linoleic acid는 정상관 경향을 보였으나, linolenic acid는 종실에서 정상관($r=0.652^*$), 속대는 부상관($r=-0.505^*$) 관계를 보였다. 2. 옥수수 종실의 불검화물을 TLC로 분리한 결과 band I (campesterol, stigmasterol, ${\beta}$-sitosterol), band II (${\Delta}^5$-avenasterol), band III (${\Delta}^7$-stigmastenol), 및 band IV (${\Delta}^7$-avenasterol)로 뚜렷하게 분리되었고, 속대는 band I~IV 이외에도 3종 이상의 band가 추가적으로 분리되었다. 3. 옥수수 종실과 속대에 함유된 phytosterol의 GC 분리 패턴을 확인한 결과 campesterol, stigmasterol 및 ${\beta}$-sitosterol의 분리능이 좋았으나, ${\Delta}^7$-avenasterol (RT 22.846), ${\Delta}^7$-stigmastenol (RT 22.852) 및 ${\Delta}^5$-avenasterol (RT 22.862)은 혼합물질 상태로는 분리가 되질 않았다. 4. 옥수수 종실의 평균 phytosterol 함량은 635.9 mg/100g, 속대는 273.0 mg/100 g으로 종실이 속대에 비해 약 2.4배 정도 phytosterol 함량이 높았다. 옥수수 종실의 phytosterol 조성은 ${\beta}$-sitosterol 80.05% > campesterol 10.5% > stigmasterol 9.46% 순이었으나, 속대는 ${\beta}$-sitosterol 59.43% > stigmasterol 31.72% > campesterol 10.98%으로 종실과 속대의 phytosterol 조성비는 다소 상이하였다. 5. 본 연구 결과를 토대로 판단할 때 옥수수 종실에 함유된 ${\beta}$-sitosterol, campesterol 및 stigmasterol의 생합성 경로에서 전구물질이 되는 ${\Delta}^7$-avenasterol, ${\Delta}^7$-stigmastenol 및 ${\Delta}^5$-avenasterol이 옥수수 속대에서 검출되는 것으로 보아 옥수수 종실의 phytosterol은 속대에서 합성되어 종실로 전이되는 물질인 것으로 추정되었다.

GC/MS를 이용한 고산 홍경천의 스테롤 구성에 대한 초기연구 (Primary study of sterols composition of Rhodiola sachalinensis by using GC/MS)

  • 김은철;이희봉;이동호;노경호
    • 분석과학
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    • 제22권3호
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    • pp.219-227
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    • 2009
  • 고산 홍경천에 포함된 스테로이드 화합물의 구성을 흡착 컬럼 크로마토그래픽 정제와 GC/MS를 이용하여 측정하였다. 스테롤은 에탄올과 디클로로메탄을 각각 초음파와 Soxhlet의 용매로 사용하여 추출하였다. 추출물은 클로로포름과 물로 액-액 추출을 수행하여 분배하였으며, 실리카 컬럼으로 정제하였으며, BSTFA를 사용하여 silyl유도 반응을 수행하였다. GC/MS를 이용하여 고산 홍경천에서 $\beta$-sitosterol, stigmasterol과 cycloartenol을 포함한 18가지 자유 스테롤과 9가지 포합체 스테롤을 검출할 수 있었다. 그중에서 cholest-5-ene-3-ol, cholesterol, stigmasterol, $\beta$-sitosterol은 스테롤 표준품으로 확인하고 정량분석을 수행하였다. 대부분의 스테롤은 클로로포름 분액에서 검출되었고, $C_{29}$는 여러 그룹 중에서 가장 많은 그룹이었다. $\beta$-sitosterol은 가장 많이 함유된 성분이며 상대함량은 45.94%이고, 차례로 ergost-7-ene-3-ol (11.33%), 4,14-dimethyl-ergosta-8,24(28)-diene-3-ol (7.07%), stigmasterol (6.09%), cycloartenol (5.43%)과 4-methyl-cholest-5-ene-3-ol (5.39%)이었다.

Steroids from the Aerial Parts of Artemisia princeps Pampanini

  • Yoo, Jong-Su;Ahn, Eun-Mi;Bang, Myun-Ho;Song, Myoung-Chong;Yang, Hye-Joung;Kim, Dong-Hyun;Lee, Dae-Young;Chung, Hae-Gon;Jeong, Tae-Sook;Lee, Kyung-Tae;Choi, Myung-Sook;Baek, Nam-In
    • 한국약용작물학회지
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    • 제14권5호
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    • pp.273-277
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    • 2006
  • Three stigmastane-type sterols and one ergostane-type sterol were isolated from the ethyl acetate soluble fraction of the aerial parts of Artemisia princeps Pampanini (Sajuarissuk). From the results of physico-chemical data including NMR, MS and IR, the chemical structures of the compounds were determined as $stigmasta-5,22-dien-3,{\beta}-ol (stigmasterol, 1),stigmast-5-en-3{\beta}-ol({\beta}-sitosterol,2), 5{\beta},8{\beta}-epidioxy-5{\beta},8{\beta}-ergosta-6,22-dien-3{\beta}-ol(ergosterol peroxide, 3),\;and\;{\beta}-sitosterol\;3-O-{\beta}D-glucopyranoside(daucosterol,4)$.

Phytochemical Studies on Reynoutriae Radix $('H\check{u}-Zh\grave{a}ng')$

  • Chi, Hyung-Joon;Kim, Hyun-Soo
    • 생약학회지
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    • 제17권1호
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    • pp.73-77
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    • 1986
  • Anthraquinones, physcion (I), mp $204{\sim}205^{\circ}$ and emodin (II), mp $254{\sim}255^{\circ}$, and $emodin-8-O-{\beta}-{_D}-glucoside$ (IV), mp $191{\sim}192^{\circ}$ together with ${\beta}-sitosterol$ glucoside (III), mp $280{\sim}282^{\circ}$ were isolated from the roots of Polygonum ellipticum Migo and P. sachalinense Fr. Schm. (Polygonaccae). Stilbene derivatives, 3,5,4'-trihydroxystibene (V), mp $258{\sim}260^{\circ}$ and $3,5,4'-trihydroxystilbene-3-O-{\beta}-{_D}-glucoside$ (VI), mp $142{\sim}144^{\circ}$ were also isolated.

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사방오리 잎의 Triterpenoid 및 Flavonoid 화합물 (Triterpenoids and Flavonoids Isolated from the Leaves of Alnus firma)

  • 유영법;;;;박종철
    • 생약학회지
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    • 제38권1호
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    • pp.76-83
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    • 2007
  • In this study, three triterpenoids, two steroids and nine flavonoids were isolated from the leaves of Alnus firma Sieb. et Zucc. On the basis of spectroscopic evidences, the structures of these compounds were established as ${\beta}$-amyrin acetate, ${\beta}$-amyrin, ${\beta}$-sitosterol, alnustic acid methyl ester, ${\beta}$-sitosterol glucoside, pinocembrin, alnustinol, quercetin, quercetin-3-O-${\alpha}$-L-arabinofuranoside, quercetin-3-O-${\alpha}$-L -rhamnopyranoside, quercetin-3-O-${\beta}$-D-glucopyranoside, myricetin-3-O-${\beta}$-D-galac-topyranoside, (+)-catechin and (-)-epicatechin.

목단의 미숙(未熟) 과실(果實)의 성분(成分)에 관한 연구 (Studies on the Chemical Constituents for the Unripe Fruits of Paeonia moutan)

  • 김영희
    • 생약학회지
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    • 제22권1호
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    • pp.22-25
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    • 1991
  • From the fresh unripe fruits of Paeonia moutan Sim. (Paeoniaceae), paeoniflorin and its acyl congeners, benzoylpaeoniflorin and benzoyloxypaeoniflorin, along with ${\beta}-sitosterol$ and methyl gallate were isolated. All compounds were identified on the basis of spectral data and chemical reactions. However, paeonol was not detected from this plant parts. These results suggested that the chemical components of the unripe fruits were virtually similar to those of root barks.

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