• Journal of Microbiology and Biotechnology
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• 제18권2호
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• pp.314-321
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• 2008

Acaricidal effects of materials derived from Diospyros kaki roots against Dermatophagoides farinae and D. pteronyssinus were assessed using impregnated fabric disk bioassay and compared with that of the commercial benzyl benzoate. The observed responses varied according to dosage and mite species. The $LD_{50}$ values of the chloroform extract of Diospyros kaki roots were 1.66 and $0.96{\mu}g/cm^2$ against D. farinae and D. pteronyssinus. The chloroform extract of Diospyros kaki roots was approximately 15.2 more toxic than benzyl benzoate against D. farinae, and 7.6 times more toxic against D. pteronyssinus. Purification of the biologically active constituent from D. kaki roots was done by using silica gel chromatography and high-performance liquid chromatography. The structure of the acaricidal component was analyzed by GC-MS, $^1H-NMR,\;^{13}C-NMR,\;^1H-^{13}C$ COSY-NMR, and DEPT-NMR spectra, and identified as plumbagin. The acaricidal activity of plumbagin and its derivatives (naphthazarin, dichlon, 2,3-dibromo-1,4-naphthoquinone, and 2-bromo-1,4-naphthoquinone) was examined. On the basis of $LD_{50}$ values, the most toxic compound against D. farinae was naphthazarin $(0.011{\mu}g/cm^2)$ followed by plumbagin $(0.019{\mu}g/cm^2),$ 2-bromo-1,4-naphthoquinone $(0.079{\mu}g/cm^2)$, dichlon $(0.422{\mu}g/cm^2)$, and benzyl benzoate $(9.14{\mu}g/cm^2)$. Additionally, the skin color of the dust mites was changed from colorless-transparent to dark brown-black by the treatment of plumbagin. Similar results have been exhibited in its derivatives (naphthazarin, dichlon, and 2-bromo-1,4-naphthoquinone). In contrast, little or no discoloration was observed for benzyl benzoate. From this point of view, plumbagin and its derivatives can be very useful for the potential control agents, lead compounds, and indicator of house dust mites.

• Archives of Pharmacal Research
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• 제29권2호
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• pp.123-130
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• 2006

1,4-Naphthoquinones are widely distributed in nature and many clinically important antitumor drugs containing a quinone moiety, such as anthracyclines, mitoxantrones and saintopin, show excellent anticancer activity. In this study, 2- or 6-substituted 5,8-dimethoxy-1,4-naphthoquinone (DMNQ) and 5,8-dihydroxy-1,4-naphthoquinone (DHNQ) derivatives were synthesized, and their cytotoxic activity against L1210 and P388 cancer cells was examined. Their antitumor activity was also assessed in mice bearing S-180 cells in the peritoneal cavity. In comparison with the DMNQ derivatives, the DHNQ derivatives exhibited more potent bioactivities than the DMNQ derivatives against both L1210 and P388 cells in vitro and S-180 cells in vivo. The $ED_{50}$ values of the DHNQ derivatives against P388 cells were in the range of 0.18-1.81 ${\mu}g/mL$ whereas those of the DMNQ derivatives were in the range of 0.26-40.41 ${\mu}g/mL$. The T/C ($\%$) values of the DHNQ derivatives, 8, 17, 18, 19, and 20, were found to be comparable to or even better than that of adriamycin. It was also observed that the 2-substituted derivatives (8, 19, 20) showed better antitumor activity than the 6-substituted derivatives (7, 17, 18) in the mice bearing S-180 cells in the peritoneal cavity.

• 대한약학회:학술대회논문집
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• 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2-2
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• pp.158.2-158.2
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• 2003

Vitamin K-related analogs induce growth inhibition in various cancer cell lines. We report that 2,3-dichloro-5,8-dihydroxy-1, 4-naphthoquinone (DDN), a naphthoquinone analog, induces mitochondria-dependent apoptosis in human promyeloid leukemic HL-60 cells. DDN induced cytochrome c release, cleavage of Bid, and activation of caspases -8, -9 and -3. Cleavage of Bid, the caspase-8 substrate, was inhibited by the broad caspase inhibitor zVAD-fmk, whereas cytochrome c release was not affected by zVAD-fmk. (omitted)

• 한국독성학회:학술대회논문집
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• 한국독성학회 2002년도 Current Trends in Toxicological Sciences
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• pp.118-118
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• 2002

It has been reported that vitamin K analogues have various pharmacological effects such as antiviral, antifungal, anticancer, and antiplatelet activities. It has also been reported that some synthetic naphthoquinone compounds showed antiplatelet activities.(omitted)

• Applied Biological Chemistry
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• 제46권3호
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• pp.268-270
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• 2003

굴피나무 지상부의 메탄을 추출물을 n-hexane, ethylacetate, n-butanol, $H_2O$으로 순차적으로 용매분획하였다. Ethylacetate 분획으로부터 silica gel chromatography를 반복하여 활성물질을 분리 정제하였다. 화합물은 NMR과 MS의 기기분석 결과 5-hydroxy-2-methoxy-1,4-naphthoquinone로 구조결정 되었다. 이 화합물은 in vivo 실험결과 토마토역병에 대하여 $100\;{\mu}g/ml$에서 76%의 방제효과를 나타내었다.

• Genomics & Informatics
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• 제20권1호
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• pp.7.1-7.13
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• 2022

2-Methoxy-1,4-naphthoquinone (MNQ) has been shown to cause cytotoxic towards various cancer cell lines. This study is designed to investigate the regulatory effect of MNQ on the key cancer genes in mitogen-activated protein kinase, phosphoinositide 3-kinase, and nuclear factor κB signaling pathways. The expression levels of the genes were compared at different time point using polymerase chain reaction arrays and Ingenuity Pathway Analysis was performed to identify gene networks that are most significant to key cancer genes. A total of 43 differentially expressed genes were identified with 21 up-regulated and 22 down-regulated genes. Up-regulated genes were involved in apoptosis, cell cycle and act as tumor suppressor while down-regulated genes were involved in anti-apoptosis, angiogenesis, cell cycle and act as transcription factor as well as proto-oncogenes. MNQ exhibited multiple regulatory effects on the cancer key genes that targeting at cell proliferation, cell differentiation, cell transformation, apoptosis, reduce inflammatory responses, inhibits angiogenesis and metastasis.

• Ecology and Resilient Infrastructure
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• 제7권1호
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• pp.72-81
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• 2020

저온수기 규조 Stephanodiscus sp.에 의한 녹조 현상은 빈번하게 일어나며, 이로 인한 수자원의 질적 변화와 정수과정에 많은 경제적 손실을 주고 있다. 선행연구를 통해 Stephanodiscus sp. 종의 친환경적 제어를 위해 개발된 생물유래 물질인 naphthoquinone (NQ) 유도체의 현장조건에서 살조효과 입증을 위해 서낙동강 수변에 5 ton 규모 mesocosm을 설치하여 현장조건에서의 살조효과와 비생물학적, 생물학적 요인을 모니터링 하였다. NQ 4-6 물질을 처리한 결과, 대상 조류인 Stephanodiscus sp.의 세포밀도가 실험 초기 5 × 10³ cells mL¹에서 급격하게 감소하여 실험 종료시인 10일차에는 0.2 × 10³ cells mL¹으로 세포 대부분이 사멸되어, 81%의 높은 살조효과가 관찰되었다. 또한, NQ 4-6 물질 접종 후 식물플랑크톤을 제외한 물리·화학적요인(수온, 용존 산소, pH, 전기전도도, 영양염)과 생물요인 (박테리아, HNFs, 섬모충, 동물플랑크톤)에 영향을 미치지 않았으며, 대조구와 처리구에서 유사한 경향이 관찰되었다. 즉, NQ 4-6 물질의 현장 적용은 규조 Stephanodiscus sp. 종의 선택적 제어뿐만 아니라, 수생 생물의 서식처와 먹이 공급을 원활하게 함으로써 건강한 수 생태계를 형성하는데 큰 역할을 할 것으로 판단된다.

• Ecology and Resilient Infrastructure
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• 제4권3호
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• pp.130-141
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• 2017

유해 남조류를 친환경적으로 제어하기 위해 개발된 생물유래 물질인 naphthoquinone (NQ) 유도체의 현장 적용 가능성을 확인하고자 하였다. 기흥 저수지 수변에 30 ton 규모의 mesocosm을 설치하여 현장 조건에서의 살조효과와 비생물학적, 생물학적 요인을 모니터링하였다. NQ 2-0 물질을 처리한 결과, 대조구에서는 대상 조류인 Microcystis sp.의 세포밀도가 지속적으로 증가한 반면, 처리구에서는 실험 초기 $7.9{\times}10^4cells\;mL^{-1}$에서 접종 후 점진적으로 세포수가 감소하여 10일차 $9.7{\times}10^2cells\;mL^{-1}$으로 대조구 대비 99.4% 감소하였다. 실험 종료시인 15일차에는 Microcystis sp. 세포수가 100% 제거되었다. 대상 조류인 Microcystis sp. 종만을 선택적으로 제어하였을 뿐만 아니라, 다른 식물플랑크톤의 성장과 식물플랑크톤 종 다양성 지수도 증진되었다. 또한, 식물플랑크톤을 제외하고 NQ 2-0 물질에 의하여 물리 화학적요인 (수온, 용존 산소, pH, 전기전도도, 영양염)과 생물요인 (박테리아, HNFs, 섬모충, 동물플랑크톤)에 영향을 미치지 않았으며, 대조구와 처리구에서 유사한 경향이 관찰되었다.

• 한국의류학회지
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• 제18권5호
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• pp.622-627
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• 1994

The purpose of this study is to investigate the adsorption rate, adsorption quantities and the UV-Cut effects of cotton fabrics treated with several UV absorbents. The result of this study were as follows: cotton fabric treated with 2,2'-dihydroxy-4- methoxy-benzophenone shows more efficient than ones treated with 4-aminobenzoic acid and 2·hydroxy-1, 4-naphthoquinone in UV absorption. This may be due to the absorption of UV light by formation of intra moleculaar hydrogen bond. The formation of hydrogen bonds between hydrogen atoms of two hydroxy groups and one oxygen atom of carboxyl group in 2, 2'-dihydroxy-4-methoxy-benzophenone would be easier than that of the other absorbents. The adsorption isotherms of 4-aminobenzoic acid and 2-hydroxy-1, 4-naphthoquinone were similar to Freundlich type, while that of 2, 2'-Dihydroxy-4-methoxy-benzophenone was Henry type. Cotton fabrics treated with Antifade MC-100 and W Cut I-2 were just alike in UV absorption, but Antifade 8001 was inferior to the others.

• 한국응용약물학회:학술대회논문집
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• 한국응용약물학회 1992년도 제1회 신약개발 연구발표회 초록집
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• pp.41-41
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• 1992

새로이 합성된 1,4-Naphthoquinone(1,4-NQ) 화합물의 세포독성의 확인과 그 작용기전을 규명코져 본 실험을 수행하였다. 분리된 흰쥐 간세포를 1,4-NQ유도체들과 반응 시켰을때 이들 중 YC 001과 YC 008은 독성을 나타냈으나 YC 012는 독성율 나타내지 아니하였다. 세포독성은 세포치사, lactate dehydrogenase 유출 및 산소소비의 억제등으로 확인하였다. 세포 독성의 기전은 mitochondria에서의 전자흐름 차단작용과 microsome에서 redox-cycling 기전에 의한 산소리디칼 생성의 두가지에 대하여 검토하였다. 분리된 mitochondria를 YC 001과 YC 008은 반응 시켰을때 mitochondria의 호흡은 완전히 억제되었다. 그러나 YC 012는 전혀 작용을 나타내지 아니하였다. 이는 간세포에 대한 독성작용과 일치하는 결과이며 따라서 mitochondria에 대한 억제 작용은 이들의 세포독성에 주요한 요인이라고 추측되었다.