• 제목/요약/키워드: Antifungal compounds

검색결과 353건 처리시간 0.026초

마늘의 유기유황성분과 생리활성 (Organosulfur Compounds from Allium sativum and Physiological Activities)

  • 권순경
    • Biomolecules & Therapeutics
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    • 제11권1호
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    • pp.8-32
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    • 2003
  • Garlic(Allium sativum L.) is one of the oldest cultivated plants and has been used throughout the world as food supplement and folk medicine for thousands of years. In modem times a number of garlic derived products are introduced on the market as health food supplement in ever growing scale. In 1844 German chemist Wertheim investigated the garlic first time chemically and thereafter many kinds of organosulfur compounds were isolated and their biological activities were elucidated scientifically. The main biological activities are antibacterial, antifungal, antithrombotic, cholesterol-lowering, antineoplastic and hepatoprotective activities. Chemical works as well as therapeutic and preventive effects of garlic are reviewed.

Design, Synthesis and Biological Activity of Certain 3,4-Disubstituted-5-mercapto-1,2,4-triazoles and Their Hydrazino Derivatives

  • Udupi, R.H.;Sudheendra, Sudheendra;Bheemachari, Bheemachari;Srinivasulu, N.;Varnekar, Rajesh;Purushottamachar, Puranik
    • Bulletin of the Korean Chemical Society
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    • 제28권12호
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    • pp.2235-2240
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    • 2007
  • 3-Aryloxy methyl-4-(N-pyrazin-2'yl carboxamido)-5-mercapto-1,2,4-triazoles (3a1-a14) were prepared starting from potassium dithio carbazinates (2a1-a14). These triazoles were then employed in the synthesis of 3-aryloxy methyl-4-(N-pyrazin-2'yl carboxamido)-5-hydrazino-1,2,4-triazoles (4a1-a14). All the newly synthesized compounds were characterized by analytical, IR, NMR spectral studies. The compounds were screened for their antibacterial, antifungal, anti-inflammatory and analgesic properties. Most of the compounds have shown significant antifungal activity while few have shown excellent anti-inflammatory and analgesic activity. An attempt is made to study the structure activity relationship (SAR).

ANTIFUNGAL AND ANTIBACTERIAL ACTIVITIES OF SOME COMPOUNDS FROM MARINE NATURAL PRODUCTS

  • Chinh, Luu-Van;Dien, Pham-Huu;Minh, Chau-Van
    • 한국응용약물학회:학술대회논문집
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    • 한국응용약물학회 1998년도 Proceedings of UNESCO-internetwork Cooperative Regional Seminar and Workshop on Bioassay Guided Isolation of Bioactive Substances from Natural Products and Microbial Products
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    • pp.174-174
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    • 1998
  • Twelve different derivatives were synthesised from chitin/chitosan[1, 2, 3]. Their structures have been determined by different physical methods. The bioassay screening on antifungal and antibacterial activities of all these compounds showed that most of them had significant activity and they can inhibite the growth of some fungi and bacterias : E. coli, S. pyogenes, F. oxysporum, P. oryzae, that caused the spoilage of fresh fruits and foods. Furthermore, all of these compounds are non-toxic (LD$\_$50/>50g/kg) and can be applied for food preservation.

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Tanshinone 단삼성분의 전신성 캔디다증에 대한 항균효과 (Antifungal Effect of Tanshinone from Salvia miltiorrhiza against Disseminated Candidiasis)

  • 한용문;주인경
    • 약학회지
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    • 제57권2호
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    • pp.119-124
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    • 2013
  • The aim of this present study was to investigate the antifungal effect of tanshinones isolated from Salvia miltiorrhiza against Candida ablicans, a polymorphic fungus. For the work, tanshinone IIA (TSN), cryptotanshinone (CTS), and dihydrotanshinone I (DTS) were chosen. Initially, their antifungal effect was analyzed by in-vitro susceptibility test. Data from the susceptibility test showed that while all of these three compounds had antifungal activity, DTS was the most potent. At $100{\mu}g$ DTS/ml, there was about 80% CFU (colony forming unit) reduction as compared to DTS-untreated C. albicans yeast cells (P<0.05). Thus, DTS was selected to determine its antifungal activity in a murine model of disseminated candidiasis due to C. albicans. Results showed that DTS enhanced resistance of mice against disseminated candidiasis. During the entire period of 30-day observation, 60% of DTS-given mice groups survived whereas control animals all died within 14 days (P<0.05). Moreover, DTS inhibited the hyphal production, one of the virulence factors of this fungus, from the blastoconidial form of the fungus. Therefore, the tanshinone appears to have antifungal activity specific for C. albicans infection, which could possibly be mediated by the blockage of hyphal production.

Isolation and structure elucidation of antifungal compounds from the antarctic lichens, Stereocaulon alpinum and Sphaerophorus globosus

  • Kim, Young-Shin;Lim, Chi-Hwan
    • 농업과학연구
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    • 제47권1호
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    • pp.183-191
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    • 2020
  • Lichens are composite organisms consisting of a symbiotic association of a fungus with a photosynthetic partner (the photobiont or phycobiont), usually either a green alga or cyanobacterium. According to more recent studies, the biological activities of lichens and lichen substances include an antibiotic activity, antitumor and antimutagenic activity against human immunodeficiency virus (HIV), allergenic activity, plant growth inhibitory activity, and enzyme inhibitory activity. This study screened lichen extracts with a potent in vitro antifungal activity against plant diseases caused by phytopathogenic fungi. The compounds were isolated from Stereocaulon alpinum and Sphaerophorus globosus, and their chemical structures were identified as methyl hematommate, methyl β-orsellinate, 5-hydroxyferulic acid, sphaerophorin, and 2-heptyl-4,6-dimethoxybenzoic acid by electron ionization mass spectrometry (EI-MS) and nuclear magnetic resonance (NMR) spectral analyses. In vitro disease control against Alternaria mali, Cochliobolus miyabeanus, Colletotrium gloeosporioides, and Verticillum dahliae was evaluated. And among the five compounds, only methyl hematommate was effective against A. mali, C. miyabeanus, and C. gloeosporioides. The compounds were isolated from these lichens, which have a similar biosynthetic pathway, respectively. This is the first report of these compounds being isolated from these lichens.

4-Isopropyl, 5-isopropyl-3-methylphenol 유도체들의 합성과 식물 병원균에 대한 항균 활성 (Antifungal activities for derivatives of 4-isopropyl-3-methylphenol and 5-isopropyl-3-methylphenol against plant pathogenic fungi)

  • 최원식;장순호;장도연;최경길;이병호;김태준;정봉진
    • 농약과학회지
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    • 제10권4호
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    • pp.249-261
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    • 2006
  • 살균활성이 있는 4-isopropyl-3-methylphenol(I)과 5-isopropyl-3-methylphenol(II)을 출발물질로 하여 ester, sulfonyl ester, carbamate, ether 및 phosphoyl ester계열의 50개 화합물들을 합성하였으며, IR, GC/MS와 $^1H$-NMR spectrum을 이용하여 합성을 확인하였다. 이 유도체들에 대한 in vitro 살균활성 실험을 10종의 식물병원균에 대하여 실시한 결과 몇 가지 화합물이 우수한 항균활성을 나타내었다. 이들 화합물을 5가지 식물병(벼도열병, 토마토역병, 오이 잿빛곰팡이병, 벼 잎집무늬 마름병, 오이탄저병)에 대하여 in vivo 항균활성을 조사하였다. 그 결과, 4-isopropyl-3-methylphenyl (2-aminothiazole-4-yl)methoxyiminoacetate(I-7a)는 벼 도열병(Pycularia oryzae)에 methyl (4-isopropyl-3-methylphenoxy)acetate(I-4d)와 methyl (5-isopropyl-3-methylphenoxy) acetate (II-4d)는 오이 잿빛곰팡이병(Botrytis cinerea)에 높은 방제활성을 나타내었다.

A Bacterial Endophyte, Pseudomonas brassicacearum YC5480, Isolated from the Root of Artemisia sp. Producing Antifungal and Phytotoxic Compounds

  • Chung, Bok-Sil;Aslam, Zubair;Kim, Seon-Won;Kim, Geun-Gon;Kang, Hye-Sook;Ahn, Jong-Woong;Chung, Young-Ryun
    • The Plant Pathology Journal
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    • 제24권4호
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    • pp.461-468
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    • 2008
  • An endophytic bacterial strain YC5480 producing antifungal and phytotoxic compounds simultaneously was isolated from the surface sterilized root of Artemisia sp. collected at Jinju area, Korea. The bacterial strain was identified as a species of Pseudomonas brassicacearum based on its 16S rRNA gene sequence analysis and physiological and biochemical characteristics. The seed germination and growth of monocot and dicot plants were inhibited by culture filtrate (1/10-strength Tryptic Soy Broth) of the strain. The germination rate of radish seeds in the culture filtrate differed in various culture media. Only 20% of radish seeds germinated in the culture media of 1/2 TSB for 5 days incubation. Mycelial growth of fungal pathogens, Colletotrichum gloeosporioides, Fusarium oxysporum and Phytophthora capsici was also inhibited by the culture filtrate of the strain YC5480. An antifungal compound, KS-1 with slight inhibitory activity of radish seed germination at 1,000 ppm and a seed germination inhibitory compound, KS-2 without suppression of fungal growth were produced simultaneously in TSB. The compounds KS-1 and KS-2 were identified to be 2,4-diacetylphloroglucinol (DAPG) and 2,4,6-trihydroxyacetophenone (THA), respectively.

길항미생물에 의한 된장 중 아플라톡신 제어 및 그 품질특성 (Control of Aflatoxin and Characteristics of the Quality in Doenjang(soybean paste) Prepared with Antifungal Bacteria)

  • 강길진;박종훈;조정일
    • 한국식품과학회지
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    • 제32권6호
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    • pp.1258-1265
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    • 2000
  • 본 연구는 아플라톡신 생성균의 생육을 억제시킬 수 있는 길항 미생물을 분리하고 그 길항미생물을 이용한 된장 제조시 아플라톡신 제어 효과와 된장의 품질에 미치는 영향을 조사하였다. 아플라톡신 생성균인 Asp. flavus와 Asp. parasiticus에 대해 길항력이 가장 강력한 균을 분리하였으며 그 균은 Bacillus 속의 특성을 보였다. 분리한 길항균과 아플라톡신 생성균을 처리하여 제조한 된장의 아플라톡신 함량은 Asp. flavus을 처리하였을 때 아플라톡신 $B_1$이 27.2 ppb에서 길항균과 함께 처리로 87.5% 감소한 3.4 ppb였으며 Asp. parasiticus을 처리하였을 때 아플라톡신 $B_1$이 30.3 ppb에서 길항균과 함께 처리로 87.8% 감소한 3.7 ppb였다. 길항균과 아플라톡신 생성균을 처리한 된장의 유리지방산, 유리당, 유기산함량은 대조구와 큰 차이 없이 비슷하였다. 유리아미노산 총 함량은 길항균과 아플라톡신 생성균 처리로 다소 낮아지는 경향을 보였으나 큰 영향을 미치지 못하였다. 주로 glutamic acid, aspartic acid, tryptophan이 감소하였다. 된장의 향기성분은 아플라톡신 생성균을 처리하였을때 대조구에 비하여 큰 변화가 없었다. 그러나 길항균 처리로 변향인 2-pentyl furan와 불쾌취인 butanoic acid류가 소멸되거나 감소하고 octadecene 화합물은 생성 되었다. 결국 분리된 길항균은 아플라톡신 생성을 억제시켰으며 된장의 품질에는 그다지 영향을 미치지 않았다.

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황기 종자의 천연 항진균성 단백질의 분리정제 및 특성검정 (Purification and Characterization of Natural Antifungal Protein from Astragal Seeds (Astragalus membranaceus L.).)

  • 구본성;류진창;정태영;김교창
    • 한국미생물·생명공학회지
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    • 제26권5호
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    • pp.379-386
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    • 1998
  • 본 연구에서는 천연 항균물질의 개발 이용을 위해 황기 종자로부터 인체에 무해한 천연 항균 단백질을 ion exchange chromatography 및 gel filteration을 이용하여, 순수 분리하고 특성을 조사하였다. 황기종자로부터 추출한 천연 항균 단백질은 Aspergillus ocraceus, Penicillium expensum, P. digitatum, Botrytis cineria의 포자 발아 및 효모인 Candida albicans의 생육을 현저하게 저해하였으며 ammonium sulfate 포화도가 0.4일 때 단백질의 침전량이 122.6 $\mu\textrm{g}$/$m\ell$로 가장 많았고 항균력도 15.2 mm로 가장 높게 나타났다. 강력한 cation exchange chromatography인 Mono-S를 이용하여 FPLC에서 단백질을 분획하였을때 첫번째 peak에서 분획된 단백질군이 항균력을 보였으며 Superose 12HR gel filteration column을 이용하여 2차 분획 하였을 때 분자량이 19 kDa되는 단일 단백질만을 순수분리 할 수 있었다. 전기 영동한 polyacrylamide gel위에 곰팡이 포자를 중층하는 bio autography로 19 kDa 단백질 band의 항균력을 직접 확인하였으며 분리된 항균 단백질의 아미노 말단의 아미 노산 22잔기를 sequencing하고 thaumatin 및 zeamatin 유사 단백질들과 상동성을 측정한 결과 50%내외의 homology를 나타내었다. 분리된 항균 단백질은 곰팡이 균사가 성장하는 선단부위에 가장 먼저 침투하여 channel을 형성함으로 osmolysis를 일으켜 곰팡이의 생육을 억제하는 것으로 추측할 수 있었다.

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Inhibitory Effects of Seaweed Extracts on Growth of Malassezia furfur and Malassezia restricta

  • Choi, Jae-Suk;Lee, Bo-Bae;Joo, Chi-Un;Shin, Su-Hwa;Ha, Yu-Mi;Bae, Hee-Jung;Choi, In-Soon
    • Fisheries and Aquatic Sciences
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    • 제12권1호
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    • pp.29-34
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    • 2009
  • Fifty seven species of common seaweed from the coast of Korea were screened for antifungal activity against Malassezia species. Seaweeds as a source of bioactive compounds are able to produce a great variety of secondary metabolites with different activities. There are numerous reports on the biological activities of seaweeds against human pathogens, fungi, and yeasts, but only few contain data regarding inhibitory effects against Malassezia sp., a major cause of dandruff and seborrheic dermatitis. To help address this paucity of information, this work was carried out to examine the antifungal effects of seaweed extracts against M. furfur and M. restricta. Of the fifty seven species of marine algae screened for their potential antifungal activity, only 17 species (29.8%) exhibited inhibitory activity. In agar disc diffusion method, the ether extracts of Corallina pilulifera, Enteromorpha linza, Laminaria japonica, Symphyocladia latiuscula and Ulva sp. showed strong antifungal activity. To identify major constituents in seaweed extracts, four selected extracts were analyzed on' a GC-MS equipped with a flame ionization detector, and compared to spectral data from databases WILEY229.LIB and NIST107.LIB. Most constituents in seaweed extracts are fatty acid-related compounds. When we evaluated any acute toxicity, the ether extracts of the selected four species were not toxic in mice. According to these results, it can be suggested that these seaweed extracts are valuable for the development of therapeutic agents in treating dandruff and seborrheic dermatitis. Further investigations to determine its bioactive compound(s) are currently in progress.