• 제목/요약/키워드: effective compound

검색결과 891건 처리시간 0.033초

The Fluorescent 7-Aminodipyrido[3,2-a:2',3'-c] phenazine(7-amino-dppz) Functionalized as an Europium Ion ($Eu^{3+}$) Sensor

  • Choi, Chang-Shik;Lee, Ki-Hwan
    • Rapid Communication in Photoscience
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    • 제1권2호
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    • pp.31-33
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    • 2012
  • The Fluorescent 7-aminodipyrido[3,2-a:2',3'-c]phenazine (7-amino-dppz, 1) is functionalized as an europium ion ($Eu^{3+}$) sensor, which showed the effective emission quenching when europium cation is chelated to the bpy site of 1 compound. The complexation ratio indicated that the 1 compound forms a 1 : 1 complex with $Eu^{3+}$.

인체유암세포주 MCF-7의 형태변화와 증식에 영향을 주는 항암활성물질, MCS-202 (Antitumoral Compound, MCS-202, an Effector on Proliferation and Morphology of Human Breast Tumor Cell Line, MCF-7)

  • 이성우;김세은;김항섭;김환묵;이정준;김영호
    • 한국미생물·생명공학회지
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    • 제21권6호
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    • pp.594-599
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    • 1993
  • In the course of screening for microbial metabolites employing human cancer cell line, we identified a mycelial extract of Streptomyces sp. 1365, which are effective on growth inhibition and morphological change of MCF-7, human breasr cancer cell line. By repeased column chromatography and recrystallization process, yellow needle crystals were obtained as an active compound and identified as resistomycin by spectral analysis.

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재첩을 이용한 음료 가공 (Processing of Corbicula elatior Beverage)

  • 강동수;최옥수
    • 생명과학회지
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    • 제11권2호
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    • pp.138-143
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    • 2001
  • Marsh calm(Corbicular elatior)with a short-term storage in raw and a law-rate of utilization has been increasing the needs to develop new marsh calm processing products for a temporary mass treatment and long-term distribution, Therefore the processing conditions of marsh calm beverage using proteolytic enzyme hydrolysis were investigated. A partial hydrolysis at 6$0^{\circ}C$ for 1 hour after adding 3% Alcalase as more effective than a hot water extraction to develop taste compounds from the marsh calm. The result of ommission test showed that nucleotides and their related compounds were contributed in the taste of the marsh calm hydrolysates rather than free amino acids. The taste of the hydrolysates was produced by association with these compounds rather than only one compound s the hydrolystes taste differently for the control when one of these compound was omitted. The hydrolysates were fractionated to molecular weight below 500 dalton to eliminate bitter taste and to improve it flavor from the hydrolysates, 0.05% bay leaf was more effective to improve the odor than other herbs.

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Alum과 PACl을 이용한 응집처리 (Chemical Coagulation Treatment Using Alum and PACl in Complex Wastewater)

  • 성일화
    • 한국환경보건학회지
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    • 제35권1호
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    • pp.53-57
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    • 2009
  • In order to treat the complex wastewater containing organic compound and solids, pre-treatment system associated with molecular separation process were investigated. The reductions of COD and turbidity were obtained after coagulation processes using Alum (Aluminium sulfate, $Al_2(SO_4)_2{\cdot}18H_{2}O$) and PACl (poly aluminium chloride as 17% $Al_{2}O_{3}$). The results of study were as follows: using variable dosage of Alum, COD removal was highest at 4,000 mg/l, and the reduction of COD and turbidity was 42% and 92%, respectively. The optimum coagulation would be effective at pH 7.3 than pH 9.0 by the addition of alum at a concentration of 6,000 mg/l and PACl was add at 4.25% in raw complex wastewater with 2,000 mg/l alum at pH 7.3, the reduction of COD was reduced by 32%. But coagulation aid experiments indicated that PACl would be more effective in sludge separation ability than COD removal efficiency.

NBD 이량체 생성물의 효율적 분리방법 (Effective Separation Method of NBD Dimer Mixture)

  • 정병훈;한정식;민성기;임진식
    • 한국추진공학회:학술대회논문집
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    • 한국추진공학회 2010년도 제35회 추계학술대회논문집
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    • pp.797-799
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    • 2010
  • 산업적으로 유용한 다중고리형 탄화수소화합물 중의 하나인 NBD 이량체 제조시, 이량화반응후 결과물에는 여러 가지 촉매와 용매, 부생성물 등이 포함되어 있다. NBD 이량체 혼합물의 수율을 증가시키기 위해서는 효율적인 분리공정이 가장 먼저 요구된다. 본 연구에서는 친환경적이고, 회수율이 높은 용매를 사용하여 NBD 이량체의 분리수율을 개선하였다.

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Biotransformation of Protopanaxadiol-Type Ginsenosides in Korean Ginseng Extract into Food-Available Compound K by an Extracellular Enzyme from Aspergillus niger

  • Jeong, Eun-Bi;Kim, Se-A;Shin, Kyung-Chul;Oh, Deok-Kun
    • Journal of Microbiology and Biotechnology
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    • 제30권10호
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    • pp.1559-1566
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    • 2020
  • Compound K (C-K) is one of the most pharmaceutically effective ginsenosides, but it is absent in natural ginseng. However, C-K can be obtained through the hydrolysis of protopanaxadiol-type ginsenosides (PPDGs) in natural ginseng. The aim of this study was to obtain the high concentration of food-available C-K using PPDGs in Korean ginseng extract by an extracellular enzyme from Aspergillus niger KACC 46495. A. niger was cultivated in the culture medium containing the inducer carboxymethyl cellulose (CMC) for 6 days. The extracellular enzyme extracted from A. niger was prepared from the culture broth by filtration, ammonium sulfate, and dialysis. The extracellular enzyme was used for C-K production using PPDGs. The glycoside-hydrolyzing pathways for converting PPDGs into C-K by the extracellular enzyme were Rb1 → Rd → F2 → C-K, Rb2 → Rd or compound O → F2 or compound Y → C-K, and Rc → Rd or compound Mc1 → F2 or compound Mc → C-K. The extracellular enzyme from A. niger at 8.0 mg/ml, which was obtained by the induction of CMC during the cultivation, converted 6.0 mg/ml (5.6 mM) PPDGs in Korean ginseng extract into 2.8 mg/ml (4.5 mM) food-available C-K in 9 h, with a productivity of 313 mg/l/h and a molar conversion of 80%. To the best of our knowledge, the productivity and concentration of C-K of the extracellular enzyme are the highest among those by crude enzymes from wild-type microorganisms.

산국으로부터 항암활성 성분의 분리 (Isolation of Cytotoxic Substances from Chysanthemum Boreale M.)

  • 양민석;남상해
    • Applied Biological Chemistry
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    • 제38권3호
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    • pp.273-277
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    • 1995
  • 60종의 생약의 methanol 추출물을 L1210세포에 대하여 1차스크리닝실험을 수행하여 항암활성물질을 검색하고, 그 중에서 비교적 세포독성이 강하게 나타나는 산국(Chrysanthemum boreale M.)에서 항암활성물질을 분리정제하였다. 산국의 용매분획물의 L1210, K562, A549세포에 대한 세포독성실험에서는 chloroform 분획에서 $ED_{50}$값이 각각 3.98, 4.28, 3.84 (${\mu}g/ml$)로 나타났다. 이 chloroform 분획에서 유효세포독성물질을 정제하여 Compound I과 Compound II를 각각 얻었으며, 이 중에서 Compound I은 L1210, K562, A549세포에 대하여 각각 $ED_{50}$값이 0.55, 0.0003, 0.001 (${\mu}g/ml$)로 강한 세포독성을 나타내었으나, Compound II는 K562에 대해서만 $ED_{50}$ 값이 4.79 (${\mu}g/ml$)의 세포독성을 나타내었다.

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Cacao bean으로부터 분리된 polyphenol 성분의 화학구조분석과 ACE 저해효과 (The chemical structure of polyphenols isolated from cacao bean and their inhibitory effect on ACE)

  • 장영렬;임무현;이만종
    • Applied Biological Chemistry
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    • 제41권1호
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    • pp.110-117
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    • 1998
  • Ghana산 cacao bean으로부터 acetone으로 추출하고 Sephadex LH-20, MCI-gel CHP-20, Bondapak $C_{18}$ 및 Fuji gel ODS $G_3$, chromatography 등을 이용하여 7종의 polyphenol 화합물(compound 1 - compound 7)을 분리 정제하였고, 이들 화합물의 화학구조를 $^1H-NMR$, $^{13}C-NMR$, IR 및 MS를 사용하여 검색하였고 아울러 angiotensin converting enzyme(ACE) 저해효과를 조사 검토하였다. 분리정제한 7종의 polyphenol 화합물의 구조를 분석한 결과, compound 1: [(+)-catechin], compound 2: [(-)-epicatechin], compound 3: [procyanidin B-1, (-)-epicatechin-$(4{\beta}{\rightarrow}8)$-(+)-catechin], compound 4 : [procyanidin B-2, (-)-epicatechin-$(4{\beta}{\rightarrow}8)$-(-)-epicatechin], compound 5: [procyanidin B-7, (-)-epicatechin-$(4{\beta}{\rightarrow}6)$-(+)-catechin], compound 6 : (procyanidin B-2,3,3'-O-digallate) 및 compound 7: [cinnamtannin A-2, (-)-epicatechin-$(4{\beta}{\rightarrow}8)$-(-)-epicatechin-$(4{\beta}{\rightarrow}8)$-(-)-epicatechin-$(4{\beta}{\rightarrow}8)$-(-)-epicatechin]임을 동정하였다. ACE의 저해효과는 procyanidin B-2,3,3'-O-digallate (compound 6)가 $100\;{\um}M$에서 94.6%로 매우 우수하였으며, (+)-catechin (compound 1), (-)-epicate -chin (compound 2), procyanidin B류 (compound 3, 4, 5) 및 cinnamtannin A-2 (compound 7)도 각각 67.9%, 61.9%, 88.6%, 82.5%, 72.2% 및 82.3%의 비교적 우수한 저해효과가 있었다. 아울러 결합방식에서는 $4{\beta}{\rightarrow}6$보다 $4{\beta}{\rightarrow}8$의 결합방식이, 그리고 procyanidin 류에서는 gallate를 갖는 물질이 이를 함유하지 많은 물질보다 더욱 높은 ACE의 저해효과를 나타내었으며, 또한 hydroxyl 기가 많을수록 효소 저해효과도 증가하는 것으로 나타났다. 이와 같은 결과는 chocolate의 주원료인 cacao bean의 polyphenol 성분 또한 녹차 등에서 볼 수 있는 생리활성효과에 손색없는 것으로 판단되고, 이러한 기능성에 기초하여 chocolate, 음료 등의 식품이나 의약품의 기능성 소재로서의 산업적 응용 가능성이 높은 것으로 사료된다.

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황련 추출물로부터 항균활성물질의 분리 및 활성 검정 (Separation and Activity Test of Antifungal Substance from C. japonica Extract)

  • 정일민;백수봉
    • 분석과학
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    • 제10권2호
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    • pp.153-159
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    • 1997
  • 황련(C. japonica)의 추출물을 이용하여 사과겹무늬병, 사관탄저병 및 사과푸른곰팡이병에 대한 항균활성을 검정함과 동시에 활성물질을 분리하여 안정성이 있는 천연식물성 농약으로서의 개발 가능성을 검토하고자 시험했던 바, 그 결과를 요약하면 공시균에 대한 황련의 조추출액 $EC_{50}$$400{\sim}500{\mu}g/mL$이고 TLC, HPLC 분석을 통한 생리활성물질은 berberine으로 동정되었고 그 함유율은 81.14%였다.

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Studies on the anti-parasitic efficacy and safety of ivermectin and pyrantel pamoate compound against Dirofilaria immitis in dogs

  • Youn, Heejeong;Ra, Jeong-Chan;Kim, Byung-Ki;Lim, Yong-Suk;Kim, Kyong-Hee;Lee, Kyong-Eun
    • 대한수의학회지
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    • 제52권1호
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    • pp.53-56
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    • 2012
  • Dirofilaria (D.) immitis is an important canine parasitic nematode in dogs. D. immitis parasitizes the right ventricle and pulmonary artery of dogs. An ivermectin and pyrantel pamoate compound (IPPC) was administered to dogs naturally infected with this parasite. IPPC is composed of 68.0, 136.0 and $272.0{\mu}g$ of ivermectin and 57.0, 114.0 and 227.0 mg pyrantel pamoate for small, middle, and large animals. Ivermectin has activity against nematodes and ectoparasites in dogs. Pyrantel pamoate is also effective against nematodes in dogs. Our results showed that this drug combination has good efficacy in D. immitis infected dogs.