• 약학회지
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• 제50권1호
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• pp.47-51
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• 2006

The roots of Dipsacus asper are used in traditional Chinese medicine as an analgesic, enhancement of liver activity, an anti-inflammatory agent and the treatment of fractures. In order to investigate the antioxidative activity, Dipsaci Radix was extracted with MeOH and fractionated with $CHCl_3$, EtOAc, BuOH and water. MeOH ex. and its solvent fractions were determined on the free radical scavenging activity by DPPH method and antioxidative activity on low density lipoprotein oxidation. The EtOAc and BuOH fractions showed antioxidative activities and from their fractions, two compounds were isolated and identified as hederagenin 3-O-${alpha}$-L-arabino pyranoside (compound 1) and O-${\alpha}$-L-arabinopyranosyl hed-eragenin 28-O-${\beta}$-D-glucopyranosyl ($1{\to}6$)-${\beta}$-D-glucopyranosyl ester (compound 2). Saponin glycoside, compound I showed anti-oxidative activity.

• 한국식품영양과학회지
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• 제28권6호
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• pp.1310-1315
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• 1999

Polyphenolic compounds widely occurring in the traditional medicine plants have been reported to possess strong antioxidant activity. The antioxidative substances of water soluble extract from leaves, stem bark, root bark and fruit powder of Cudrania tricuspidata were tested in three different in vitro experimental models. In oxidation models using DPPH( , ' diphenyl picrylhydrazyl) method, Fe2+ induced linoleic acid peroxidation, and autooxidation of hepatic microsomal membranes, the antioxidative activities of water soluble extract from stem bark were strong than that from leaves and root bark. Fruits of Cudrania tricuspidata contained the highest amounts of polyphenolic compounds among the parts of this plant. The changes in polyphenolic compound contents of fruit powder caused by heat treatment (20oC, 40oC, and 60oC) were also monitored. After water blanching, contents of phenolic compounds was increased slightly in the following order; 20oC(1454mg), 40oC(1487mg), and 60oC(1511mg). These results supports that water soluble extracts from Cudrania tricuspidata contain antioxidative compounds.

• 한국식품저장유통학회지
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• 제8권2호
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• pp.231-238
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• 2001

The concentrations of total polyohenolic compound from extract of Paulownia tomentosa Stued. were water-soluble extract 7.98%, methanol extract 12.30% and ethanol extract 11.63%. The free radical scavenger activities of three extracts at the levels of 0.5% were higher than that of BHT(butylated hydroxytoluene). In antioxidative activities measured the concentrations of TBARS(thiobabituric acid reactive substances) in tissues microsome induced with Fe$\^$++/ascorbate, the water-soluble extract was errdctively suppressed in liver and spleen. In antioxidative activities determined by thiocyanate method against lipid peroxidation using linoleic acid, the methanol extract showed the higher compared with other extracts, but BHT showed the highest antioxidative activity. These results suggest that fruit extracts of Paulownia tomentosa Stued. showed to have relatively high concentrations of polyphenolic compounds and antioxidative activities.

• 생약학회지
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• 제48권1호
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• pp.46-50
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• 2017

This study was conducted to investigate the antioxidative activities and tyrosinase inhibition effects of fractions from the distilled water extract of Inonotus obliquus. Moreover, GC-MS based analysis with trimethylsilyl (TMS) derivatization was carried out for active compound in the extract of I. obliquus. In DPPH radical scavenging ability, $SC_{50}$ values of the ethyl acetate fraction was 0.393 mg/ml as a result of the most effective than other fractions. Meanwhile, aqueous fraction showed higher effect in tyrosinase inhibitoty activity. In GC-MS based analysis with TMS derivatization, 7 compounds including syringic acid, vanillic acid and protocatechuic acid were observed in ethyl acetate fraction, and oxalic acid is the main compound in aqueous fraction. As a result, it was confirmed that oxalic acid in aqueous fraction from the distilled water extract of I. obliquus was a compound showing tyrosinase inhibition effect.

• Journal of the Korean Wood Science and Technology
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• 제31권5호
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• pp.43-48
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• 2003

회화나무잎에서 3종의 화합물을 단리하였으며, 기기분석 결과 hypogallic acid, kaempferol, quercetin으로 각각 동정하였다. 이들 단리 물질의 항산화 활성은 라디칼 소거능으로 측정하였으며, 항산화 활성은 100 ㎍/ml의 농도에서 각각 98.2%, 96.2% 그리고 90.2%를 나타내었고 이 중 화합물 1 (hypogallic acid)과 화합물 2 (kaempferol)의 경우는 합성 항산화제인 BHT보다 높은 항산화 활성을 나타내었다.

• 약학회지
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• 제53권3호
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• pp.130-137
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• 2009

In this study, isolation of antioxidative compounds was performed for development of anti-oxidizing agent. $CHCl_3$, $H_2O$, 30%, 60% MeOH, MeOH fractions were examined antioxidative activity by DPPH, test of inhibition on NO production. It was revealed that 30%, 60% MeOH and $CHCl_3$ fractions had significant antioxidative activity. In 30% MeOH and 60% MeOH, $CHCl_3$ fraction, six compounds were isolated and elucidated as adenosine(I), guanosine(II), peucedanol 7-O-$\beta$-D-apiofuranosyl(1$\rightarrow$6)-$\beta$-glucopyranoside(III), peucedanol 7-O-$\beta$-D-glucopyranoside(IV), peucedanol(V) and scopoletin(VI) by physicochemical data and spectroscopic methods. (Negative FAB-MS, $^{1}H-NMR$, $^{13}C-NMR$). The results from antioxidative activity screening for the each compound showed that compound IV was relatively superior antioxidant ability. In anti-inflammatory activation assay, compound III, IV, VI had concentration-dependent-activity and compound IV had superior anti-inflammatory ability. These results suggest that Peucedani Radix might be developed as a potent anti-oxidative, anti-inflammatory agents and ingredients for related functional foods.

• 한국식품영양과학회지
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• 제30권4호
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• pp.726-731
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• 2001

밤 가공공장에서 폐기되고 있는 밤의 귀피를 항산화 기능성 자원으로 활용하고자 밤 귀치의 methanol 추출물 및 용매획분을 benzoic acid 수산화법으로 hydroxyl radical 소거능과 ferric thiocyanate법으로 과산화물생성 억제능을 시험하였다. 대부분의 획분에서 항산화성을 보였으며 특히 ethyl acetate 획분에서 BHA나 $\alpha$-tocopherol과 거의 유사한 rkdgkshydroxyl radical 소거능과 지질과산화물생성 억제능을 보였다. Ethyl acetate 획분으로부터 항산화성 물질을 분리하기 위하여 Sephadex LH-20 column chromatography 및 prep HPLC를 행하여 단일 물질로 정제하였다. 분리 정제된 물질을 $^{1}$H-NMR과 $^{13}$C-NMR로 구조 분석한 결과 gallic acid로 동정하였다. 페놀산을 GC로 분석한 결과 밤 귀피의 주요 페놀산으로 ellagic acid(172.22 mg%) 와 gallic acid(107.39 mg%)가 확인되었다.

• 생약학회지
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• 제31권2호
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• pp.185-189
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• 2000

This study was carried out to investigate the structure of antioxidative constituents and the free radical scavenging effect of the main ingredients from Galla Rhois(Rhus javanica Linne). Antioxidative activities of n-hexane, EtOAc and BuOH extracts of Galla Rhois were similar or even higher than that of natural (tocopherol) or synthetic antioxidant (BHA). It is suggested that major fractions for the antioxidative activity of Galla Rhois were the n-hexane, EtOAc and BuOH extract compartments. In the subsequently experiment, one active compound from n-hexane extract, three active compounds from EtOAc extract and one active compound from BuOH extract were isolated. Their chemical structures were identified as syringic acid, protocatechuic acid, gallic acid methylester, gallic acid and $1,2,3,4,6- penta-O-galloyl-{\beta}-D-glucose$ on the basis of the speculation of spectral data and chemical reaction. Among the compounds, protocatechuic acid, gallic acid methylester and $1,2,3,4,6- penta-O-galloyl-{\beta}-D-glucose$ showed most potent radical scavenging effect using DPPH method.

• 생명과학회지
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• 제14권5호
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• pp.863-867
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• 2004

식물성 성분 중에서 생리활성 인자를 탐색할 목적으로 솔잎의 수용성 추출물에 의한 항산화 활성을 DPPH법, thiocyanate법, TBA법 및 microsome 생 체 막 지 질 과산화물 생성정도를 TBARS법으로 측정 하고, 총 폴리페놀 함량을 측정하였다. 솔잎 수용성 추출물의 총 폴리페놀 화합물 함량은 1.61%이었으며, DPPH 측정법에서는 짙은 자색의 탈색되는 정도로 나타내는 전자 공여능이 솔잎 수용성 추출물의 0.1% 농도에서 BHT와 비슷한 수준으로 항산화 활성이 높게 나타났다. 간 microsome을 이용한 생체막 지질 과산화 억제정도는 솔잎 수용성 추출물의 0.1% (67.7%)>0.05% (63.1%)>0.01%(28.2%) 순으로 농도에 비례하여 증가하였다. Linoleic acid 산화 실험계를 이용한 thiocyanate법에서는 0.01%, 0.05%, 0.1%의 농도에서 모두 반응 7일째까지 대조구에 비해 매우 강한 항산화 활성을 보였으며, TBA법에서는 반응 6일째까지 는 0.1%>0.05%>0.01%의 순으로 농도 증가에 따라 항산화 활성도 높게 나타났다. 이상의 결과에서 솔잎 수용성 추출물 중에는 in vitro 항산화 실험에서 항산화 활성을 나타내는 생리활성 성분이 존재하는 것으로 볼 수 있으므로 천연 항산화제로서의 가능성을 시사하였다.

• Archives of Pharmacal Research
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• 제28권8호
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• pp.885-888
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• 2005

Jacaranone and related compounds (1-3) were isolated, along with three triterpenes (4-6), from the fresh fruits of Ternstroemia japonica. The compounds were identified as jacaranone (1), 3-hydroxy-2,3-dihydrojacaranone (2), 3-methoxy-2,3-dihydrojacaranone (3), 3-O-acetyl­oleanolic acid (4), 3-O-acetylursolic acid (5), and ursolic acid (6). Jacaranone and its derivatives were isolated for the first time from Theaceae. Of the isolated compounds, compound 3 is a new compound. Jacaranone (1) exhibited weak antioxidative effect on 1, 1-diphenyl-2-picryl-hydrazyl (DPPH) radical.