• 아시안잔디학회지
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• 제20권1호
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• pp.57-63
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• 2006

이 연구는 식물유래 천연물, TGR-N1의 잔디진균병에 대한 방제효과를 조사하기 위해 수행되었다. In vitro실험에서 TGR-N1은 잔디진균병에 대해 항균효과를 나타내었다. TGR-N1의 500배, 1000배액은 Rhizoctonia solani AG 1-1, Rhizoctonia solani AG2-2, Rhizoctonia cerealis, Sclerotinia homoeocarpa, Colletotrichum graminicola 에 대해 강한 항균력을 나타내었다. 그러나 Pythium spp.에 대해서는 항균효과가 없었다. TGR-N1의 Rhizoctonia solani AG 1-1, Rhizoctonia solani AG2-2에 대한 포장방제 실험결과, TGR-N1 500배액의 방제가는 각각 86.1%와 83.3%의 방제가를 나타내었다. 이 연구 결과 식물유래 천연물 TGR-N1의 항균 활성이 확인되었는 바 천연물 농약으로서의 잠재성을 보여 주었다.

• Natural Product Sciences
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• 제21권4호
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• pp.237-239
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• 2015

Sarcotragin C (1), a new sesterterpene metabolite was isolated from a Sarcotragus sp. sponge collected from Chuja Island, Korea. On the basis of the combined spectroscopic analyses, the structure of this compound was determined to be a linear norsesterterpene containing a leucine-derived ${\gamma}-lactam$ moiety. This compound exhibited moderate cytotoxicity against K562 and A549 cell-lines.

• 자연과학논문집
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• 제14권2호
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• pp.33-40
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• 2004

유기물이 포함된 황산아연 폐수로부터 황산아연을 회수하기위해서는 유기물의 제거가 필수적이다. 폐수 속에 포함된 유기물을 2차 오염물질이 거의 발생하지 않게 처리하기 위하여 오전 산화법과 흡착법을 병용하여 처리함으로서 효과적으로 유기물을 제거 할 수 있었다. 과량의 황산은 산화아연을 처리하여 황산아연 7수염을 제조함으로써 과량의 황산을 처리할 수 있었다. 폐수 1kg을 처리하여 740g의 황산아연 7수염을 얻었다.

• KSBB Journal
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• 제16권3호
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• pp.269-273
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• 2001

218종의 목본식물 자원으포부터 높은 항율력올 보인 Schima wallichii subsp. liukiuellsis로부터 항균활성물질을 추출, 정제하였다. Schim$\alpha$의 향균물질 추출에 가장 적합한 용매는 70% 에탄올이었으며, 계젤에 따른 항균활성은 차이를 보이지 않았고, 부위별로는 가을에 채취한 수피가 가장 좋았다. 조추출물을 유가용매로 정제하여 최종적으혹 buthanol 분획올 얻었고, 이를 silica gel과 sephadex LH-20 및 HPLC분석을 통 하여 흰색결정의 항균물질 Compound I을 얻었다. 항균물질은 UV, IR, MS분석 결과 aglycone으로 ${\alpha}$-sitosterol에 rhamnose, galactose, glucose가 1:1:1로 결합된 물질로 추정되었다. Compound I의 미생물에 대한 MIC는 3종의 bacteria에 L 1.25 g/L, 2종의 fungi에 5.0 g/L로 나타났으며, 효모에 대한 MIC는 0.04 g/L로 매우 높게 나타났다. Compound I은 천연 보존제, 의약품 등으로의 향후 개발이 기대된다.

• Journal of Microbiology and Biotechnology
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• 제9권6호
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• pp.709-715
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• 1999

A series of antifungal compounds were obtained from the methanol extract of the mycelium from marine actinomycetes M428 which was identified as a Stereptomyces species by fatty acid composition and biochemical characteristics. These compounds were purified by combined chromatographic techniques and the structures were characterized with spectroscopic methods including 1D and 2D NMR, and mass spectrometry as sn-l lysophosphatidyl inositols. The side chains were established by chemical degradation followed by GC analysis to be 14-methyl pentadecanoic acid (iso-palmitic acid, i-C16:0, compound A) and 13-methyl tetradecanoic acid (iso-pentadecanoic acid, i-C15:0, compound B). These compounds displayed highly selective antifungal activity against C. albicans with MIC values of $5{\;}\mu\textrm{g}/ml$ (compound A) and $2.5{\;}\mu\textrm{g}/ml$ (compound B), while it had almost negligible antibiotic activity against E. coli and P aerogenosa with MIC value higher than $50{\;}\mu\textrm{g}/ml$ and no cytotoxic activities against human myeloma leukemia K562 ($IC_{50}>100{\;}\mu\textrm{g}/ml$).

• The Korean Journal of Physiology and Pharmacology
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• 제17권3호
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• pp.217-222
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• 2013

We reported that ailanthoidol, a neolignan from Zanthoxylum ailanthoides and Salvia miltiorrhiza Bunge, inhibited inflammatory reactions by macrophages and protected mice from endotoxin shock. We examined the anti-inflammatory activity of six synthetic ailanthoidol derivatives (compounds 1-6). Among them, compound 4, 2-(4-hydroxyphenyl)-5-(3-hydroxypropenyl)-7-methoxybenzofuran, had the lowest $IC_{50}$ value concerning nitric oxide (NO) release from lipopolysaccharide (LPS)-stimulated RAW264.7 cells. Compound 4 suppressed the generation of prostaglandin (PG) $E_2$ and the expression of inducible NO synthase and cyclooxygenase (COX)-2 induced by LPS, and inhibited the release of LPS-induced pro-inflammatory cytokines from RAW264.7 cells. The underlying mechanism of compound 4 on anti-inflammatory action was correlated with the down-regulation of mitogen-activated protein kinase and activator protein-1 activation. Compound 4 is potentially an effective functional chemical candidate for the prevention of inflammatory diseases.

• Natural Product Sciences
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• 제11권1호
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• pp.41-44
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• 2005

Chemical investigation of the aerial parts of Chloranthus japonicus Sieb. led to the isolation a new compound, 9-hydroxy heterogorgiolide (1) and $isofraxidin-7-O-{\beta}-D-glucopyranoside$ (2), the isolation of which is reported for the first time from this plant, along with the known components, ${\beta}-sitosterol,\;{\beta}-sitosterol-3-O-{\beta}-D-glucopyranoside$, palmitic acid and octacosanoic acid. The structures of compound 1 and 2 were determined on the basis of spectroscopic data including two dimensional NMR and high resolution MS.

• 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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• 제20권2호
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• pp.86-90
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• 2014

Phytochemical investigation of the 80% MeOH extract from the leaves of Hosta longipes resulted in the isolation of sixteen compounds (1 - 16). The structures of the compounds were elucidated by spectroscopic methods to be methyl 10,10-dimethoxydecanoate (1), methyl 10-hydroxy-8E,12Z-octadecadienoate (2), methyl coriolate (3), trans-phytol (4), phytene-1,2-diol (5), phyton (6), (3S,5R,6S,7E,9R)-7-megastigmene-3,6,9-triol (7), (3S,5R,6S,9R)-3,6,9-trihydroxymegastigman-7-ene (8), shikimic acid (9), p-coumaramide (10), trans-N-p-coumaroyltyramine (11), cis-N-coumaroyltyramine (12), tryptophan (13), thymidine (14), adenosine (15), and deoxyadenosine (16). Compound 1 was synthesized, but not yet isolated from natural source, and compounds 2-16 were isolated for the first time from this plant source.

• Natural Product Sciences
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• 제10권6호
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• pp.315-320
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• 2004

Alpha-viniferin was previously isolated as a cyclooxygenase (COX)-2 inhibitor from Carex humilis (Cyperaceae) and is an oligomeric stilbene compound with benzofuran (BF) moieties in its chemical structure. In the present study, a chemically synthetic BF compound, named as 3,3-dimethyl-2,3,4,6,7,8,9,10,11,12,13,14,15,16,17,18-hexadecahydro-1H-benzo[b] cyclopentadeca[d]furan-1-one, was discovered to inhibit bacterial lipo polysaccharide (LPS)-induced prostaglandin $E_2$ $(PGE_2)$ production in macrophages RAW 264.7. The BF compound exhibited a selectively preferred inhibitory effect on COX-2 activity over COX-1 activity. Furthermore, BF compound inhibited LPS-induced COX-2 expression at transcription level. As a down-regulatory mechanism of COX-2 expression shown by BF compound, suppression of nuclear factor $(NF)-{\kappa}B$ activation has been demonstrated. BF compound inhibited LPS-induced $NF-{\kappa}B$ transcriptional activity and nuclear translocation of $NF-{\kappa}B$ p65, in parallel, but did not affect LPS-induced degradation of inhibitory ${\kappa}B{\alpha}$ protein $(I{\kappa}B{\alpha})$. Taken together, anti-inflammatory effect of BF compound on $PGE_2$ production was ascribed by its down-regulatory action on LPS-induced COX-2 synthesis in addition to inhibitory action on enzyme activity of COX-2.