• Natural Product Sciences
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• 제14권1호
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• pp.16-20
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• 2008

Three flavonoids (1 - 3) and three phenolic compounds (4 - 6) were isolated from the whole plant of Geranium thunbergii Sieb. et Zucc (Geraniaceae). Their structures were determined by chemical and spectral analysis. These compounds were examined for the inhibitory activity of IL-6 production in $TNF-{\alpha}$ stimulated MG-63 cell. Among the isolated compounds, gallic acid (4) and gallic acid methyl ester (6) showed potent inhibitory activity.

• Journal of Microbiology and Biotechnology
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• 제19권7호
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• pp.681-684
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• 2009

This study was carried out to evaluate the inhibitory effect of Flammulina velutipes extracts on tyrosinase activity and to identify its biologically active component. The ethyl acetate and n-butanol extracts showed potent tyrosinase inhibitory activities. Subsequently, fractions of the n-butanol extract showed only a partial tyrosinase inhibitory activity. The most active compound of tyrosinase inhibitory activity was identified from the ethyl acetate extract as 1',3'-dilinolenoyl-2'-linoleoylglycerol (LnLLn) by comparing its mass, $^1H-$, and $^{13}C-NMR$spectral data with those previously reported in the literature. LnLLn showed tyrosinase inhibitory activity with an $IC_{50}$value of 16.1 ${\mu}g/ml$. These results suggest that the ethyl acetate extract of F. velutipes could be applicable for the development of a new whitening agent.

• 한국식품과학회지
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• 제30권1호
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• pp.224-229
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• 1998

국내산 곡류의 에탄올 및 메탄올 추출물로부터 콜레스테롤 생합성계에서 가장 중요한 율속효소로 알려져 있는 HMG-CoA reductase 저해활성을 검색하였다. HMG-CoA reductase activity 측정용 효소원은 cholestyramin을 급여하여 사육 한 후 밤 12시경에 간율 적출하여 얻어진 microsome을 freeze-thaw방법으로 조제하였고 효소활성은 spectrophotometric assay로 측정하였다. 그 결과 각 시료 추출물을 $100{\;}{\mu}g/assay$ 되게 첨가한 경우 HMG-CoA reductase 억제활성은 에탄올 추출물에서는 수수가 가장 높은 활성을 보였고 다음은 흑임자였으며 나머지는 활성이 미미하거나 전혀 없는 것으로 나타났다. 메탄올 추출물에서는 기장이 가장 높은 활성을 나타내었고 다음은 수수였으며 그 다음은 메밀, 흑미의 순으로 나타났다. 또한 추출물에서 높은 억제활성을 나타내었던 수수와 기장 메탄올 추출물을 각종 용매로 분획하여 활성을 검토한 결과 수수와 기장 모두 헥산 획분에서 가장 높은 활성을 나타내었다.

• Food Science and Biotechnology
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• 제18권1호
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• pp.239-244
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• 2009

In the current study, inhibitory activity of 8 selected Korean edible plants of Lamiaceae family against $\alpha$-glucosidases, prepared from rat small intestine acetone powder was evaluated. Total flavonoids and oxygen radical absorbance capacity (ORAC) were also investigated. Methyl alcohol extracts of Scutellaria indica (SI) had the highest $\alpha$-glucosidase inhibitory activity relevant for potentially managing hyperglycemia, followed by Clinopodium gracile (CG) and Thymus quinquecostatus (TQ). These 3 species also showed significant antioxidant activity in ORAC system. The $\alpha$-glucosidase inhibitory activity of the extracts was compared to selected phenolics. Among the standard phenolics tested quercetin which was major flavonoid in the extracts had the highest $\alpha$-glucosidase inhibitory activity. CG, TQ, and SI which had high quercetin content and ORAC values also exhibited significant sucrase inhibitory activity. Results suggested that selected 3 Korean Lamiaceae species have the potential development of effective dietary strategy for postprandial hyperglycemia and oxidative stress-linked diabetes complications.

• 한국축산식품학회지
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• 제32권5호
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• pp.678-684
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• 2012

본 연구는 tyrosinase 활성 저해효과가 있는 젖산균인 L plantarum M23 균주를 이용하여 멜라닌 형성을 억제하기 위한 최적 발효유 제조조건을 설정하는데 그 목적이 있다. 3수준 4인자 중심합성 계획법을 통해 실험설계하여 반응표면분석법을 사용하였다. 독립변수로는 yeast extract 농도(%, $X_1$), 포도첨가량(%, $X_2$), 배양온도($^{\circ}C$, $X_3$), 배양시간(h, $X_4$)을 설정하였고, 종속변수로는 pH(pH, $Y_1$), 종합적 기호도(score, $Y_2$)와 tyrosinase inhibitory activity(%, $Y_3$)를 설정하였으며, tyrosinase inhibitory activity가 가장 높고 pH는 4.4를 동시에 만족하는 최적화를 실시한 결과 yeast extract 농도는 0.13%, 포도 첨가량은 2.95%, 배양 온도는 $37.1^{\circ}C$, 배양 시간은 14.8 h일 때 예상되는 pH는 4.42, 기호도는 7.06, tyrosinase inhibitory activity은 86.65%이었으며, 실제 실험 결과 pH는 4.35, 기호도는 6.86, tyrosinase inhibitory activity은 84.05%로서 큰 차이를 나타내지 않았다. 이러한 결과를 토대로 melanin 생합성과정의 key enzyme인 tyrosinase을 활성억제하는 L. plantarum M23을 이용한 발효유는 피부의 미백 작용과 노화 억제 작용에 기여할 것으로 사료되었다.

• Archives of Pharmacal Research
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• 제13권2호
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• pp.132-135
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• 1990

Polyhydroxystilbenes including resveratrol were reported to competitively inhibit monoamine oxidase-A-without structural relation with substrates and cynthetic inhibitors for the enzyme. We attempt to explore a plausible mechanism for their inhibitory activity on MAO-A. All the polyhydroxystilbenes tested showed the antioxidant activity on liver homogenate. Furthermore, the antioxidant activity turned out to closely correlate with the MAO-A inhibitory activity.

• 한국작물학회지
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• 제60권4호
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• pp.498-503
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• 2015

This study was conducted to evaluate the cytotoxicity and ${\alpha}-Amylase$, ${\alpha}-Glucosidase$, pancreatic lipase inhibition in vitro by different solvent fractions from the roots of Codonopsis lanceolata. The values of $IC_{50}$ against Calu-6 cell showed a high effect in n-hexane fraction ($10.13{\mu}g/mL$) whereas DW fraction exhibited the weakest inhibition on cell viability, having an $IC_{50}$ value of over $1,000{\mu}g/mL$. The values of $IC_{50}$ against HCT-116 cell showed the highest activity in n-BuOH fraction ($102.01{\mu}g/mL$), followed by n-hexane fraction ($145.85{\mu}g/mL$), methylene chloride fraction ($332.02{\mu}g/mL$), ethyl acetate fraction ($462.93{\mu}g/mL$) and DW fracion ($>1,000{\mu}g/mL$). ${\alpha}-Amylase$ inhibitory activity in methylene chloride fraction and ethyl acetate fraction was found to have a higher inhibitory effect with 24.5% and 25.6% than the other fractions. The highest ${\alpha}-Glucosidase$ inhibitory activity was observed from the ethyl acetate fraction extract, while the extract of DW fraction showed the lowest level of inhibitory activity at given experiment concentration. The pancreatic lipase inhibitory activity of C. lanceolata was found to have a higher the effect in ethyl acetate fraction. Inhibition of lipase activity of the ethyl acetate fraction and n-hexane fraction showed a relatively high, while the extract of DW fraction showed the lowest level at given experiment concentration. These results suggested that the roots of C. lanceolata may assist in the potential biological activity on carbohydrate, lipid Inhibitory activity and anticancer activity.

• 약학회지
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• 제46권6호
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• pp.387-391
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• 2002

In vitro $\beta$-lactamase inhibitory activity of 6-exomethylene sulbactam compounds (CH-120, 130, 140, 145, 150, 155) was compared with clavulanic acid, sulbactam and tazobactam. The inhibitory activity of CH-140 was stronger than sulbactam and clavulanic acid against Type II, III, IV, TEM enzymes and stronger than tazobactam against Type IV enzyme. The inhibitory activity of CH-145 was stronger than sulbactam and clavulanic acid against Type I, II, III, IV, TEM enzymes and stronger than tazobactam against Type III, IV enzymes. The in vitro antimicrobial activity of CH-140 and CH-145 combined with piperacillin and ceftriaxone was compared with the sulbactam and tazobactam against $\beta$-lactamase producing 31 strains. But, synergistic activity of CH-140 and CH-145 was inferior to tazobactam.

• 한국미생물·생명공학회지
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• 제27권5호
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• pp.354-358
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• 1999

In order to know the antifungal characteristics of saturated fatty acids having 6 to 12 carbons, their minimum inhibitory concentrations (MICs) and minimum fungicidal concentrations (MFCs) were estimated against Saccharomyces cerevisiae. Fatty acids from C6 to C11 exhibited increasing activity with chain length, but C12 fatty acid did not show activity at all. In relation to antifungal modes of actions, fatty acids investigated showed on inhibitory activity toward the plasma membrane H+-ATPase of Saccharomyces cerevisiae. Their inhibitions to the glucose-induced acidification and ATP hydrolysis caused by the proton pump were found to be in common wiht antifungal activities. At the test concentration of 1mM, hexanoic acid (C6) showed the lowest inhibition of about 30%, while undecanoic acid(C11) showed the strongest inhibition of over 90%. In addition, as seen with antifungal activity, the inhibitory activity of dodecanoic acid (C12) was suddenly reduced to less than 50%.

• Advances in Traditional Medicine
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• 제7권4호
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• pp.379-384
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• 2007

Two medicinal plant of Sundarbans mangrove forest has been tested for the evaluation of growth inhibitory and antibacterial activity. The methanol extract of Xylocarpus granatum stem bark showed potent wheat rootlet ($IC_{50}=0.01{\mu}g/ml$) and shoot ($IC_{50}=0.23{\mu}g/ml$) growth inhibitory activity in a concentration related manner. The growth inhibitory activity was markedly decreased in residual methanol extract. The methanol extract showed antibacterial activity (MIC > 3 mg/ml) against Bacillus subtilis, Staphylococcus aureous and Proteus vulgaris. The residual methanol extract did not show any antibacterial activity. The results suggest the bioactive principle(s) of Xylocarpus granatum may be relatively non polar compound(s). The methanol extract and residual methanol extract of Sarcolobus globosus stem showed poor wheat rootlet and shoot growth inhibitory activity and no antibacterial activity.