• 한국작물학회지
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• 제68권2호
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• pp.59-68
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• 2023

본 연구는 국립식량과학원에서 육성한 단옥수수 자식계통의 phytochemical 함량과 항산화 활성을 평가하여 고기능성 단옥수수 품종 육성을 위한 기초 자료로 이용하고자 수행하였다. 1. Carotenoid 함량이 가장 높은 계통은 KSE34 (1239.3±6.4 mg 100 g^-1), flavonoid 함량이 가장 높은 계통은 KSE6(68.6±9.6 mg CE 100 g^-1)으로 나타나 각 계통마다 화합물의 함량이 다양하였다. Phenolic compound 함량은 대부분의 단옥수수 자식계통에서 풍부하게 나타났으며, KSE8과 KSE25가 가장 높은 함량을 가진 계통이었다. 2. DPPH와 ABTS 라디칼 소거능으로 평가한 국내 단옥수수 자식계통의 항산화 활성 중 DPPH 활성은 계통 간에 다양하였으나, ABTS 활성은 차이가 적게 나타났다. KSE30과 KSE6이 각각 108.4±9.6 mg TE 100 g^-1, 104.2±12.8 mg TE 100 g^-1로 가장 좋은 DPPH 활성을 보인 계통이었으며 KSE47, KSE4, KSE21은 낮은 활성을 보였다. 3. 계층 군집 분석과 주성분 분석을 사용하여 단옥수수 자식계통의 농업적 특성을 비교하고 분류하였다. Carotenoid, polyphenol, flavonoid 함량이 높고 항산화 활성이 우수한 4개 계통(KSE6, KSE30, KSE34, KSE40)이 선발되었고, 향후 조합 능력 평가를 거쳐 고기능성 단옥수수 품종 개발에 활용할 것이다.

• Natural Product Sciences
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• 제10권3호
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• pp.101-103
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• 2004

Two Lignans Phyllanthin and Hypophyllanthin, and a steroid ${\beta}-sitosterol$ has been isolated from the leaves of Phyllanthus debilis and their structures were established by spectral analysis and direct comparison with authentic samples. This is the first report of occurrence of these compound from P.debilis.

• 약학회지
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• 제22권1호
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• pp.1-7
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• 1978

Two yellowish oily liquid compounds, $C_{6}H_{6}O_{3}$(A) bp $189^{\circ}$, $n^{20}_{D}$ 1.3697 and $C_{7}H_{8}O_{3}$(D) bp $164^{\circ}$, $n^{20}_{D}$1.5075, were isolated from root of Codonopsis pilosula (Franch.) Nannfeldt (Campanulaceae). Their structures were identified as 5-(hydroxymethyl)-2-furaldehyde(A) and 5-(methoxymethyl)-2-furaldehyde(D). The latter is a new compound among the known natural products.

• 약학회지
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• 제35권3호
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• pp.147-153
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• 1991

Chemical constituents of fruits, leaves and barks of Acanthopanax senticosus forma inermis were studied. Their fruits have higher contents of crude ash, crude protein, crude fat, fructose and glucose than those of other Acanthopanax species, and contained larger amount of glutamic acid and malic acid among amino acid and organic acid, respectively. The compounds identified from their barks and leaves, were $\beta$-sitosterol and stigmasterol, sesamin, savinin, syringaresinol diglucoside, oleanolic acid, chiisanoside and polyacetytene ($C_9H_{10}O_2$, mp. 62~63).

• Archives of Pharmacal Research
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• 제29권11호
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• pp.952-956
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• 2006

A phytochemical investigation of stems from Salvadora persica resulted in the first isolation of four benzylamides from a natural source. The isolated compounds were identified as butanediamide, $N^{1},\;N^{4}$-bis(phenylmethyl)-2(S)-hydroxy-butanediamide (1), N-benzyl-2-phenylacetamide (2), N-benzylbenzamide (3) and benzylurea (4). The structure elucidation was accomplished using spectroscopic methods, especially 2D NMR and HREIMS. Compound 2 revealed a significant inhibitory effect on human collagen-induced platelet aggregation, and a moderate antibacterial activity against Escherichia coli.

• Journal of Microbiology and Biotechnology
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• 제33권7호
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• pp.941-948
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• 2023

Metabolites from medicinal plants continue to hold significant value in the exploration and advancement of novel pharmaceuticals. In the search for plants containing compounds with anti-inflammatory effects, we observed that the ethanol (EtOH) extract obtained from the aerial components of Gouania leptostachya DC. var. tonkinensis Pit. exhibited substantial suppression of nitric oxide (NO) in vitro. In a phytochemical study on an EtOH extract of G. leptostachya, 11 compounds were purified, including one unreported compound namely gouanioside A (1). Their chemical structures were unambiguously determined through the use of various spectroscopic techniques, such as 1 and 2D NMR, IR, and HR-ESI-MS, and by producing derivatives via chemical reactions. The EtOH extract, fractions, and a new compound exerted inflammatory effects by altering NO synthesis in murine RAW264.7 macrophage cells stimulated with lipopolysaccharide. The underlying inflammatory mechanism of the new compound 1 was also explored through various in vitro experiments. The results of this study indicate the potential usefulness of new compound 1 from G. leptostachya as a treatment for inflammatory diseases.

• 생약학회지
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• 제27권1호
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• pp.15-19
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• 1996

In the course of phytochemical studies of Chrysanthermi Flos(Chrysanthemum indicum L., Compositae), two compounds were isolated by repeated column chromatography. Compound 1 is identified as adenosine on the basis of spectroscopic means and comparison with an authentic standard. Compound 2 is determined to be a new alkyl alcohol glycoside, 1-octen-3-ol $3-O-{\beta}-D-xylopyranosyl(1{\rightarrow} 6)-{\beta}-D-glucopyranoside$ on the spectroscopic evidence. Compounds 1 and 2 are reported for the first time from this plant.

• Natural Product Sciences
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• 제24권2호
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• pp.115-118
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• 2018

Herein, we reported the phytochemical investigation of whole thallus Sumatran lichen, Stereocaulon graminosum Schaer, and isolated a mono aromatic compound, ethyl haematommate (1). The structure of compound 1 have been established based on spectroscopic data and confirmed by single crystal X-ray structure analysis.

• Natural Product Sciences
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• 제17권3호
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• pp.181-182
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• 2011

Phytochemical investigation of Lycium chinense fruits led to isolation of a new pyrrole compound. The structure of this compound was confirmed as a 5-methoxymethyl-lH-pyrrole-2-carbaaldehyde, a new natural product, by interpretation of 1D ($^1H$, $^{13}C$) and 2D (HMQC, HMBC) spectroscopic data along with HRMS and IR spectroscopic data.

• 약학회지
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• 제51권2호
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• pp.140-144
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• 2007

Polygonum cuspidatum has been used as treatments of dermatitis, gonorrhea, inflammation, and hyperlipidaemia in traditional medicine. We examined liver protective effect on CCl$_4$ inducing hepatotoxicity and anti-oxidative activity by TBA method. Phytochemical examination of Polygonum cuspidatum led to the isolation and characterization of emodin 8-O-${\beta}$-D-glucopyranoside (compound 1), and trans-resveratrol 3-O-${\beta}$-D-glucopyranoside (compound 2). Compounds 1 and 2 enhanced the inhibition of anti-lipid peroxidative effects in liver homogenate. In chemical parameters obtained from serum analysis, compounds 1 and 2 also revealed significant decrease in hepatotoxicity. These results suggested that the antraquinone and stilbene which were isolated from Polygonum cuspidatum might be used as therapeutic agent of hepatitis.