• 제목/요약/키워드: Oleanolic acid

검색결과 179건 처리시간 0.026초

얇은막 크로마토그래피에 의한 인삼(人蔘)의 근(根) 엽(葉) 및 경(莖)의 saponin 및 sapogenin화합물(化合物) 동정(同定) (Identification of Saponin and Sapogenin in Root, Leaf and Stem of Ginseng by Thin Layer Chromatography)

  • 최강주;김석창;김만욱;남기열
    • Applied Biological Chemistry
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    • 제30권4호
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    • pp.340-344
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    • 1987
  • 인삼(人蔘)의 근(根) 및 지상부(地上部) 사포닌을 얇은 막 크로마토그래피로 동정(同定)한 결과(結果) 인삼근(人蔘根)에 함유된 사포닌 중 $ginsenoside-Re,\;-Rg_1,\;-Rc,\;-Rf,\;-Rb_2$$-Rb_1$ 은 각각 엽(葉)과 경(莖)에서도 동정(同定)되었으며 이외에도 엽(葉)에서 10개과 경(莖)에서 9개의 unknown spot를 동정(同定)할 수 있었다. 또한 부위별(部位別) 총(總)사포닌을 50% 초산으로 온화한 조건에서 산(酸) 가수분해(加水分解)하여 생성(生成)된 prosapogenin의 조사결과(調査結果), panaxadiol계 사포닌 및 ginsenoside-Re의 산(酸) 가수분해물(加水分解物)인 $ginsenoside-Rg_3$$ginsenoside-Rg_2$가 각각 동정(同定)되었다. 한편 근(根), 엽(葉) 및 경(莖)의 총사포닌을 황산 가수분해(加水分解)하여 sapogenin 조사결과, 근(根)에서는 panaxadiol, panax atriol 및 oleanolic acid가 검출되었고, 엽(葉)과 경(莖)에서는 panaxatriol 및 panaxadiol만이 동정(同定)되었다.

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피부 섬유아세포에서 광나무 추출물의 항 노화 효과 (Anti-Aging Effect of Ligustrum japonicum Extract in the Human Fibroblast Cells)

  • 김윤정;이유리;천종우;이현상
    • 대한화장품학회지
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    • 제36권4호
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    • pp.295-301
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    • 2010
  • 본 연구에서는 천연 추출물을 이용하여 화장품 원료를 개발하고자 다양한 천연물을 대상으로 조사하였고 그중 광나무 추출물을 선별하여 주름 개선 원료로 사용하고자 하였다. 고성능액체크로마토그래피를 수행하여 주름 개선 효과로 잘 알려진 oleanolic acid 31.06 %와 ursolic acid 8.92 %를 확인하였다. 제조된 광나무 추출물은 피부 섬유아세포에서 procollagen type I과 hyaluronan synthase-3의 발현을 증가시키고 matrix metalloproteinase (MMP)-1, MMP-2, cyclooxygenase-2의 발현을 감소시킬 뿐 아니라 elastase의 활성을 억제하여 주름 개선 기능을 갖는 것을 확인하였다. 따라서 광나무 추출물은 주름개선 화장품 소재로 개발될 수 있는 잠재력이 있다.

조협 (皂莢, Gleditsiae Fructus) n-hexane 추출물이 NC/Nga Tnd mouse의 아토피 피부염에 미치는 영향 (The Effects of Gleditsiae Fructus n-hexane Extract on Atopic Dermatitis of NC/Nga Tnd Mouse)

  • 구은진;김윤희
    • 대한한방소아과학회지
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    • 제35권1호
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    • pp.76-103
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    • 2021
  • Objectives This study was designed to examine the effect of Gleditsiae Fructus n-hexane (GSF_Hx) on two different groups (on the LPS-induced activation of Raw264.7 cells in vitro, and on the DNCB-induced activation of atopic dermatitis NC/Nga Tnd mice in vivo) to find index components and active components of Gleditsiae Fructus. Methods GSF_Hx was analyzed by HPLC profiling and confirmed echinocystic acid (EA), oleanolic acid (OA) as index components of Gleditsiae Fructus. Using GSF_Hx, EA, OA, we investigated IL-6, TNF-α, NO production by ELISA analysis and evaluated manifestations of MAPKs transcription factors and NF-κB p65 translocation by western blotting. During In vivo study, atopic dermatitis was induced on NC/Nga Tnd mice by DNCB and administered GSF_Hx, EA, OA orally, and checked skin lesions and measured skin clinical score. Serum IgE level, Th1 and Th2 cytokines secretion and modulating molecular mediators and immune cells in the spleenocyte culture supernatant, PBMCs, ALN and dorsal skin were also measured by real-time PCR. Then, skin rash was evaluated and mast cell distribution was verified by H&E and toluidine blue staining on dorsal skin. Results It is possible that GSF_Hx, EA and OA reduce inflammation and allergic response of atopic dermatitis by suppressing Th1 and Th2 cytokines secretion and modulating molecular mediators and immune cells. They also had moisturizing effect by raising vitality of ceramide in dorsal skin of atopic dermatitis NC/Nga Tnd mice. However, EA particularly had better overall activity data than OA, that EA could be a more effective active component of Gleditsiae Fructus than OA. Conclusions Based on the inflammatory reduction property with moisturizing effect, GSF_Hx may play a role in effective treatment for atopic dermatitis.

Preparation and Adsorption Properties of PA6/PSMA-OA Molecularly Imprinted Composite Membranes in Supercritical CO2

  • Zhang, Qing;Zhang, Xingyuan;Zhang, Wencheng;Pan, Jian;Liu, Ling;Zhang, Haitao;Zhao, Dong;Li, Zhi
    • Bulletin of the Korean Chemical Society
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    • 제32권9호
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    • pp.3348-3354
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    • 2011
  • Oleanolic acid (OA) as template molecule, polyamide-6 (PA6) as basement membrane and poly(styrene-comaleic acid) (PSMA) were used to prepare PA6/PSMA-OA molecularly imprinted composite membranes by phase inversion method in supercritical $CO_2$ ($ScCO_2$). The template molecule (OA), [poly(styrene-co-maleic anhydride) (PSMAH), PSMA, molecularly imprinted membranes (MIMs) imprinting OA and MIMs after elution were all characterized by Fourier transform infrared spectroscopy (FTIR). The conditions that were the mass ratio between PSMA and OA from 3:1 to 8:1, temperature of $ScCO_2$ from $35^{\circ}C$ to $50^{\circ}C$ and pressure of $ScCO_2$ 12 MPa to 17 MPa were studied. It was obtained the largest adsorption rate and purity of OA after adsorption of the resultant MIMs, 50.41% and 96.15% respectively. After using PA6 film and non-woven fabrics as basement membrane respectively, it was found that smaller aperture of PA6 was used as basement membrane, a higher adsorption rate and a higher purity of OA after adsorption of the MIMs were obtained, and so were the stability and reproducibility of the resultant MIMs. After template molecules being removed, the MIMs had effective selectivity hydrogen bonding to separately bind in the binary components to the template molecules-oleanolic acid.

상륙성분(商陸成分)에 관(關)한 연구(硏究)(II) -자리공, 양자리공, 섬자리공의 성분비교(成分比較)- (Constituents of Phytolacca Species (II) -Comparative Examination on Constituents of the Roots of Phytolacca americana, P. esculenta and P. insularis-)

  • 우원식;지형준;강삼식
    • 생약학회지
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    • 제7권1호
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    • pp.51-54
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    • 1976
  • Steroid and terpenoid constituents of 3 species of genus Phytolacca have been examined by TLC. All contained ${\alpha}$-spinasterol, its glucoside and acylated glucoside, jaligonic acid and its methylester, esculentic acid and its methylester, and 10 phytolaccosides. Jaligonic acid was the major free triterpenoid and phytolaccoside E was the major saponin in all plants. Bayogenin, oleanolic acid, spergulagenic acid, acinosolic acid, hederogenin, and their derivatives contained in other Phytolacca spp. were not found in these plants.

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Anti-Platelet Pentacyclic Triterpenoids from Leaves of Campsis grandiflora

  • Jin Jing Ling;Lee Yong Yook;Heo Jung Eun;Lee Sanghyun;Kim Jeong Mi;Yun-Choi Hye Sook
    • Archives of Pharmacal Research
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    • 제27권4호
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    • pp.376-380
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    • 2004
  • Five pentacyclic triterpenoids, oleanolic acid (1), hederagenin (2), ursolic acid (3), tormentic acid (4) and myrianthic acid (5), were isolated from the methanol extract of the leaves of Campsis grandiflora, and structures of the compounds were established by the spectroscopic methods. Compounds 2, 3, 4, and 5 were isolated for the first time from the genus Campsis. All of the compounds ($IC_{50}$: 45.3, 32.8, 82.6, 42.9 and $46.2{\mu}M$ respectively) were as equivalently inhibitive as acetylsalicylic acid ($IC_{50}:57.0{\mu}M$) on epinephrine induced platelet aggregation.

상기생의 트라이테르펜 및 페놀성 성분의 면역조절 작용 (Immunodulatory Activity of Triterpenes and Phenolic Compounds from Viscum Album L.)

  • 박대섭;최상진;김경란;이선미;이강노;표석능
    • Biomolecules & Therapeutics
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    • 제11권1호
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    • pp.1-4
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    • 2003
  • Plants are known as important source in the search for new drugs. The twelve compounds from Viscum album (Loranthaceae), lupeol (1), betulonic acid (2), betulinic acid (3), terminic acid (4), ursolic acid (5), $\beta$-sitosterol (6), $\alpha$-spinasterol (7), oleanolic acid (8), 5-hydroxy-1-(4′-hydoxyphenyl)-7-(4"-hydroxyphenyl)-hepta-1-en-3-on (9), 2′-hydroxy-4′,6′-dimethoxychalcone-4-O-glucoside (10), 2′-hydroxy-4′,6′-dimethoxychalcone-4-O-[apiosyl(l$\longrightarrow$2)]glucoside (11) and syringin (12) were evaluated for their immunomodulatory properties. Compounds 6 and 11 induced the macrophage tumoricidal activity and the lymphocyte blastogenesis. In addition, these compounds stimulated the macrophages to induce the production of TNF-$\alpha$ and NO. These findings suggest that compounds 6 and 11 are modulating various elements of the host immune response.

Design, Synthesis and Evaluation of Pentacyclic Triterpenoids Similar to Glycyrrhetinic Acid Via Combination of Chemical and Microbial Modification as Glycogen Phosphorylases Inhibitor

  • Zhu, Yuyao;Zhang, Jian;Huang, Xiaode;Chen, Bin;Qian, Hua;Zhao, Botao
    • Journal of Microbiology and Biotechnology
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    • 제28권11호
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    • pp.1876-1882
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    • 2018
  • A series of pentacyclic triterpenoids similar to glycyrrhetinic acid were designed and synthesized via the combination of chemical modification and microbial catalysis. All products were screened for the glycogen phosphorylases inhibitory activities in vitro. Within this series of derivatives, compound 5 displayed good inhibitory activities with $IC_{50}$ value of $27.7{\mu}M$, which is better than that of the other derivatives and glycyrrhetinic acid. Structure-activity relationship (SAR) analysis of these inhibitors was also discussed.

백화사설초(百花蛇舌草)의 성분(成分)에 관한 연구(硏究) (Studies on the Constituents of Oldenlandia diffusa)

  • 김영희
    • 한국약용작물학회지
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    • 제3권2호
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    • pp.91-95
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    • 1995
  • 국내(國內)에서 생산(生産)된 백화사설초(百花蛇舌草) Oldenlandia diffusa(WiIId.) Roxb. 의 전초로 부터 얻은 MeOH extract를 $CHCl_3, EtOAc$ 및 BuOH로 분획하여 얻은 fraction으로 부터 column chromatography를 실시하여 3종의 화합물을 분리하였다. 이들의 이화학적(理化學的) 및 분광학적(分光學的) data를 종합하여 화합물 I의 화학구조는 ${\beta}-sitosterol$에 소양(小量)의 stigmasterol이 함유된 sterol이며, 화합물 II는 ursolic acid이고, 화합물 III은 ${\beta}-sitostero\;3-0-{\beta}-D-glucoside$임을 밝혔다. 이 식물은 다양한 생리활성(生理活性)이 보고(報告)된 ursolic acid의 중요한 자원식물(資源植物)이 될 수 있음을 본실험을 통하여 밝혔으며 문헌(文獻)에 보고(報告)된 oleanolic acid는 함유(含有)되어 있지 않음을 알았다.

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작약(芍藥)의 성분연구(成分硏究) (3);Triterpenoid의 분리 (Phytocheical Studies on Paeoniae Radix (3);Triterpenoids)

  • 김주선;김윤정;이소영;강삼식
    • 생약학회지
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    • 제39권1호
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    • pp.37-42
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    • 2008
  • From the 70% EtOH extract from the roots of Paeonia lactiflora (Paeoniaceae), nine triterpenoids were isolated and identified as ${\beta}-amyrin$ (1), 24-methylenecycloartanol (2), betulinic acid (3), oleanolic acid (4), hederagenin (5), 30-norhederagenin (6), 30-norarjunolic acid (7), arjunolic acid (8), and $3{\beta},4{\beta},23-trihydroxy-24,30-dinorolean-12,20(29)-dien-28-oic$ acid (9) by spectroscopic methods. Among these compounds, 1, 2, 7, 8 and 9 were isolated for the first time from this plant.