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        검색결과 26

        1.
        2016.12 KCI 등재 구독 인증기관 무료, 개인회원 유료
        To increase the availability of Maxillaria species and cultivars, we investigated the volatile floral scents in eight species and cultivars of M. tenuifolia, M. variabilis, M. variabilis 'Alba', M. variabilis 'NxO', M. variabilis 'Brown', M. variabilis 'Red', M. variabilis 'Nana', and M. sangnine. The volatile components were analyzed using headspace-solid phase microextraction-gas chromatography-mass spectrometry (HS-SPME-GC-MS). We identified 46 volatiles in eight species and cultivars of Maxillaria. α-pinene, eucalyptol, trans-β-ocimene, α-copaene, and β-caryophyllene were major flavor components in the eight Maxillaria species and cultivars. A principle component analysis (PCA) showed that M. tenuifolia, M. variabilis, M. variabilis 'NxO', M. variabilis 'Brown', M. variabilis 'Nana', and M. sangnine (major components: sesquiterpenes) were located closely together on t he s core p lot. However, M. variabilis 'Alba' and M. variabilis 'Red' (major components: monoterpenes) were located closely on the score plot and not analyzed coconut flavor.
        4,000원
        2.
        2010.05 KCI 등재 구독 인증기관 무료, 개인회원 유료
        팽화홍삼으로부터 용매추출, 용매분획 및 silica gel column chromatography를 반복하여 두 개의 화합물을 분리하였다. 이들 두 화합물의 결정특성, 녹는점, 비선광도, Infrared spectrum 분석 결과, TLC에서의 Rf값, HPLC에서의 retention time 및 NMR 데이터를 측정하여 고찰한 결과 두 개의 화합물은 20(S)-ginsenoside Rg3와 ginsenoside Rg5임을 확인할 수 있었다. 특히 1H- 및 13C-NMR 데이터를 HSQC 및 HMBC와 같은 2D-NMR 실험을 통하여 더욱 정확하게 동정하였다.
        4,000원
        4.
        2020.04 KCI 등재 서비스 종료(열람 제한)
        천연미백소재를 개발하기 위하여 대산(마늘)을 포함한 총 10종의 약용식물 혼합물을 발효하여 얻은 발효물로부터 tyrosinase inhibition 활성을 확인하고, 이로부터 신규한 화합물 1종 외 3종의 활성 성분을 분리하였다. 마늘복합발효물의 영양성분 13항목을 분석하여 기능성 식품 소재로의 활용가능성을 확인하였다. 발효원액의 tyrosinase 저해효과는 88.6%로 나타났고, 활성성분의 분리를 위하여 EtOAc, n-BuOH 및 H2O로 분배, 추출하였다. 이중 수득률이 가장 높은 EtOAc 분획물(47g)로부터 silica gel 및 ODS column chromatography를 반복하면서 TLC 와 효소저해 효과로부터 확인한 활성분획을 순차적으로 분리하였다. 화합물의 화학구조를 NMR 및 MS 등의 스펙트럼으로 분 석한 결과 phenylpropanoid류의 신규 화합물인 2,4,5- trihydroxy-benzenepropanoic acid (1) (1.9 ㎎) 및 화합물 1과 동량으로 혼재하는 2,3,5-trihydroxy-benzenepropanoic acid (2)를 확인하였다. 이외에 2,4-dihydroxy-hydrocinnamic acid (3) (3.3 ㎎) 및 (+)sesamin (4) (6.1 ㎎)을 분리·동정하였다. 이 화합물들이 향후 본 조성물의 지표성분 및 기능성 성분으로 활 용된다면 기업에서의 원천기술 확보를 통한 제품개발과 산업화에 매우 유용할 것으로 사료된다.
        5.
        2016.10 서비스 종료(열람 제한)
        Background : Acanthopanax sessiliflorus (Rupr. et Maxim) Seem, belonging to the Araliaceae family, is widely distributed in Korea, China, and Japan. The plants belonging to Acanthopanax species are traditionally used in Korea as anti-rheumatoid arthritis, anti-inflammatory and anti-diabetic drugs and are recognized to have ginseng-like activities. A simple and sensitive high-performance liquid chromatographic (HPLC) method was developed and validated for independent analysis of major compounds and chlorogenic acid in A. sessiliflorus fruits. Chlorogenic acid was reported that prevent cancer and cardiovascular disease in vivo. Also, it has antioxidant effect in vitro test. In the previous experiment, chlorogenic acid were found in A. sessiliflorus fruits. This study was performed to identification of the major compounds and investigate the method validation for the determination of chlorogenic acid in A. sessiliflorus fruits. Methods and Results : Three major compounds were recorded on a Varian Unity Inova AS-400 FT-NMR spectrometer and analyzed by the new HPLC analysis method. HPLC analysis was carried out using an Waters e2695 and PDA detector. The new analyasis method was validated by the measurement of intra-day, inter-day precision, accuracy, limit of detection (LOD, S/N=3), and limit of quantification (LOQ, S/N=10) of chlorogenic acid. The results showed that the correlation coefficient (R2) for the calibration curves of chlorogenic acid was 0.997 in terms of linearity. The limit of detection (LOD) and limit of quantification (LOQ) were 0.565 ㎍/ml and 2.88 ㎍/ml, respectively. There was no interfering peak observed each other and HPLC system was suitable for analysis showing goodness of peak and high precision. Conclusion : This method is suitable to detect and quantify major compounds in A. sessiliflorus fruits. Furthermore, the result will be applied to establish chlorogenic acid as an standard compound for A. sessiliflorus fruits.
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