• 제목/요약/키워드: silica-gel column chromatography

검색결과 631건 처리시간 0.032초

산겨릅나무 줄기에서 페놀성 글루코사이드의 분리 (Isolation of Phenolic Glucosides from the Stems of Acer tegmentosum Max)

  • 허종문;양은주;최선하;송경식
    • Applied Biological Chemistry
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    • 제49권2호
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    • pp.149-152
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    • 2006
  • 산겨릅나무(A. tegmentosum)의 성분 연구를 위하여 줄기를 MeOH로 추출하여 $CH_2Cl_2$, n-BuOH 및 $H_2O$ 순으로 분획하였다. n-BuOH fraction에 대하여 silica gel과 RP-18 column chromatography를 행하여 2종의 화합물을 분리하였다. 이들 화합물의 구조는 spectral data를 문헌치와 비교하여 methyl gallate $4-O-{\beta}-D-glucoside(1)$와 salidroside(2)로 동정하였다. 이들 화합물은 산겨릅나무에서 처음으로 분리되었다.

오미자(Schizandra chinensis) 추출물의 항균물질 분리 (Isolation of the Antimicrobial Compounds from Omija (Schizandra chinensis) Extract)

  • 이상호;이영춘;윤석권
    • 한국식품과학회지
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    • 제35권3호
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    • pp.483-487
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    • 2003
  • 오미자 essential oil에 존재하는 항미생물 활성물질을 분리하기 위하여 hexane-ether 용매계를 이용하여 silica gel column chromatograph를 실시하였다. 여기서 얻은 6개 획분의 S. aureus에 대한 항미생물성을 조사하였고, 항미생물성이 큰 획분의 GC-MS를 통하여 9개의 성분을 동정하였다. 한편 오미자 정유, citronellol 및 terpineol을 첨가한 배지에서 S. aureus와 E. coli의 생육억제 효과를 관할한 결과 E. coli 보다는 S. aureus에 대한 항균력이 큰 것으로 나타났다. 그리고 오미자 정유를 농도별로 첨가한 배지중에서 S. aureus와 E. coli에 대한 경시적 생육억제 효과를 조사한 결과 S. aureus의 경우 오미자 정유 첨가군에서 $6{\sim}12$시간까지 생육이 억제되었으나 E. coli의 경우에는 생육억제 효과가 거의 없었다. 따라서 citronellol과 terpineol이 오미자 정유성분 중에 존재하는 중요 항균물질임을 확인하였다.

오매 추출물에 함유된 Ursolic Acid에 의한 Helicobacter pylori의 Urease 활성억제 (Ursolic Acid Isolated from Mume Fructus Inhibits Urease Activity of Helicobacter pylori)

  • 박찬엘;박창호
    • Korean Chemical Engineering Research
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    • 제51권5호
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    • pp.591-596
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    • 2013
  • 전통식물한약재에 대한 데이터베이스, 한국식물자원에 대한 문헌 및 선행연구 결과에 근거해 선정한 6가지의 식물 한약재(연교, 소목, 형개, 황련, 소엽, 오매)의 에탄올(70%) 추출물 중에서 오매 추출물이 Helicobacter pylori의 urease 활성에 가장 강한 억제력을 나타내었다. 극성이 다른 용매를 사용한 회분식 용매추출과 칼럼 크로마토그래피를 이용한 3단계 분리공정을 통하여 오매 추출물에 함유된 유효성분을 분리 정제하였다. NMR 분석에 의해 정제된 오매 추출물에 함유된 활성성분이 ursolic acid로 확인되었다. 본 실험결과는 오매에 함유된 이 성분이 항생제를 대신하여 H. pylori 제거에 활용될 수 있음을 시사하였다.

대추로부터 베튜리닉 산과 알피톨릭 산의 분리 및 정량 (Isolation and Quantitative Analysis of Betulinic Acid and Alphitolic Acid from Zyziphi Fructus)

  • 배기환;이상명;이은실;이준성;강종성
    • 약학회지
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    • 제40권5호
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    • pp.558-562
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    • 1996
  • Betulinic acid and alphitolic acid, the triterpenoids of Zyziphi Fructus, were isolated with silica gel column chromatography and used as the standard substances for the analysis. The compounds were determined with HPLC and HPTLC. They were separated on reversed phase column (Nova-Pak C18) with 0.05M Na2HPO4-methanol (19:81) in HPLC and detected at 210nm. Separation on HPTLC precoated silica gel F254 plates was carried out with chloroform-methanol (6:1) and the separated compounds were reacted with p-anisaldehyde and detected at 540nm. The contents of betulinic acid and alphitolic acid in Zyziphi Fructus from four different regions in Korea were in the range of 2.9~3.8% and 3.2~3.9%, respectively.

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간흡충에 대한 살충성물질에 관한 연구 (VI) - 향어 체표면 점액내 살충성물질의 구조 확인 (The Wormicidal Sibstance of Fresh Water Fishes on Clonorchis sinensis(VI) - Struture Identification of Purified Clonorchicidal Sudstance from Epidermal Mucus of Cyprinus carpio nudus)

  • 이재구;김평길;안병준
    • 약학회지
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    • 제31권1호
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    • pp.33-39
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    • 1987
  • In order to elucidate the defence mechanism of Cyprinus carpio nudus to Clonorchis sinensis, clonorchicidal substance in the epidermal mucus of this fish was isolated by silica gel column and thin layer chromatography and analyzed for its chemical nature by UV, IR and NMR-spectroscopy. The epidermal mucus of the fish was extracted by ethyl ether and separated into 2 fractions by column chromatography using petroleum ether/chloroform(30/70,v/v) as first solvent and methanol as second solvent. The second fraction with greyish white colour showed clonorchicidal effect. The second was again fractionated into greyish white precipitate and clonorchicidal greenish yellow supernatant fraction, by adding petroleum ether and standing the mixture for 5 days at $5^{\circ}C$. The latter was divided into 7 fractions in column chromatography with acetone/ benzene (10/90, v/v) as carrier. The fraction on equivalent to the spot of Rf. 0.225 value among them disclosed the strongest clonorchicidal effect. By this purification procedure, clonorchicidal substance was purified 154-fold with 0.9% yield from the mucus of the fish, and 10mg of the final fraction killed tne metaceicariae in 22 min. Infra red, nuclear magnetic resonance and ultraviolet spectrometric analysis of the purified substance revealed that the substance is linoleic acid. According to the results of the present studies it seemed that this fish could not be proper intermediate host of Clonorchis sixensis, and that defence mechanism of this fish to the worm seems to be correlated with clonorchicidal substance in epidermal mucus.

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상백피 추출물중 Listeria monocytogenes 증식억제 물질의 분리 및 효과 (Growth Inhibition of Listeria monocytogenes by Pure Compound Isolated from Extract of Morus alba Linne Bark)

  • 안은영;한지숙;신동화
    • 한국식품과학회지
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    • 제29권6호
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    • pp.1236-1240
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    • 1997
  • 상백피를 75% 에탄올로 추출하여 얻은 조 추출물을 다시 용매별로 순차 분획 후 Listeria monocytogenes 5균주에 대하여 증식저해 효과를 비교한 후 항균활성 물질을 확인하였다. 활성이 있는 획분을 1차 및 2차 column chromatography를 통하여 활성 물질을 순수 분리하여 활성 물질 획분(F-5')을 얻었고 이 획분을 tryptic soy broth에 100 및 300 ppm을 첨가하여 Listeria monocytogenes를 증식시킨 결과 배양시간에 따라 뚜렷한 균수의 감소가 관찰되어 높은 살균효과가 인정되었으며 처리된 균체의 세포적의 비정상적인 형태가 전자현미경을 통하여 관찰되었다.

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익모초의 약효 성분에 관한 연구(I) (Studies on Active Principles of Leonurus sibiricus)

  • 신순희
    • 생약학회지
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    • 제15권2호
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    • pp.104-107
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    • 1984
  • The essential oil fraction of Leonurus sibiricus was analyzed by TLC and gas chromatography. By utilizing silica gel column, a ketone compound, m.w. 167, was isolated from the essential oil. The essential oil showed considerably the diuretic action, but the water extract exhibited weak action. This diuretic action of the water extract was potentiated by combined administration of essential oil. On the isolated rabbit's uterus the essential oil decreased spontanous movement and showed relaxation.

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Streptomyces sp. YJB-599가 생산하는 Genistein의 분리 및 정제

  • 함병권;배동훈;유주현
    • 한국미생물·생명공학회지
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    • 제24권3호
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    • pp.311-315
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    • 1996
  • A cytotoxic material was produced by strain No. 5-99 which was isolated from soil. Analyzing the cell wall components, LL-diaminopimelic acid was identified. From the existance of glycine in the cell wall, this strain was identified to Streptomyces sp. which has cell wall chemotype I and peptidoglycan type A3 connected by glycine. So, we named this strain to Streptomyces sp. YJB-599. The Active material was purified through solvent extraction, silica gel column chromatography and crystallized to needle-shaped white -crystal. Analyzing the structure of this crytal by instrumental analysis and database, it was determined to genistein.

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Antitumor and Antiinflammatory Constituents from Celtis sinensis

  • Kim Dae Keun;Lim Jong Pil;Kim Jin Wook;Park Hee Wook;Eun Jae Soon
    • Archives of Pharmacal Research
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    • 제28권1호
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    • pp.39-43
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    • 2005
  • Eight compounds were isolated from the methanolic extract of the twigs of Celtis sinensis through repeated silica gel and Sephadex LH-20 column chromatography. Their chemical structures were elucidated as two triterpenoids, germanicol and epifriedelanol, two amide compounds, trans-N-caffeoyltyramine and cis-N-coumaroyltyramine, two lignan glycoside, pinoresinol glycoside and pinoresinol rutinoside, and two steroids by spectroscopic analysis.

Antioxidative Components from the Aerial Parts of Lactuca scariola L.

  • Kim, Dae-Keun
    • Archives of Pharmacal Research
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    • 제24권5호
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    • pp.427-430
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    • 2001
  • The antioxidant activity of Lactuca scariola (Compositae) was investigated by measuring the radical scavenging effect on DPPH (1,1-diphenyl-2-picrylhydrazyl) radical. The methanolic extract of the aerial parts of Lactuca scariola showed strong radical scavenging activity. The EtOAc soluble fraction exhibited a stronger activity than the others, and was purified by silica gel and Sephadex LH-20 column chromatography. Quercetin-3-O-$\beta$-D-glucopyranoside, luteolin-7-O-$\beta$-D-glucopyranoside, luteolin, quercetin and kaempferol, together with 11$\beta$,13-dihydrolactucin were isolated from the EtOAc soluble fraction as active ingredients.

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