• 제목/요약/키워드: Methyl C(2)

검색결과 1,763건 처리시간 0.031초

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.

인삼 지용성성분인 유전독성억제효과와 작용기전 (Antigenotoxicity of Ginseng Petroleum Ether Extract and its Action Mechanism)

  • 허문영
    • 한국식품위생안전성학회지
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    • 제13권3호
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    • pp.243-251
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    • 1998
  • 백삼(Pampx ginseng C.A. Meyer, 4년근)을 가루로 한 다음 petroleum ether로 24시간 추출 후 감압 농축시켜 인삼 석유에텔추출물(GPE)로 하였다. 이때 GPE의 수율은 평균 2.24%였다. 또한 GPE를 petroleum ether 소량에 녹이고 petroleum ether:ether 용매계열로 silicagel column chromatography에 의한 partition을 실시하여 P1, P2, P3 , P4, P5의 5개의 분획을 얻었다. 본 실험에서는 소핵생성 물질인 N-methyl-N-nitrosourea(MNU) 및 benzo(a) pyrene[B(a)P]를 이용하여 소핵생성억제실험을 하였따. 상기의 5가지 분획 중에서 MNU에 대해서는 GPE, P1, P2에서 억제효과가 나타났다. 한편, B(a)P에 대해서는 GPE, P1, P2, P3 , P4, P5 모두에게 억제효과를 나타내었다. 그러나 여러 가지 활성을 보인 분획 중에서 여러 가지 양성대조물질들에 대해서 가장 두드러져 보이는 것은 P2였다. P2는 MNU, B(a)P 모두에 대해서 GPE와 유사한 억제경향을 보이면서 억제활성은 크게 나타난T다. EK라서 P2가 GPE가 보이는 소핵생성억제효과에 깊은 관련이 있는 물질로 판단되었다. 이와 같은 유전독성억제효과의 작용기전을 알기 위하여 B(a)P의 대사에 미치는 영향을 연구한 결과 GPE와 P2는 S-9 mix에 의해 유도된 B(a)P 대사를 억제시켰으며, DNA-B(a)P binding도 감소시켰다. 한편, MNU에 의한 DNA binding 과 O6-methyl guanine 및 7-methyl guanine 생성에 있어서도 억제적인 경향을 나타내었다. 따라서 GPE와 P2는 B(a)P와 같은 2차 발암 물질과 MNU와 같은 알킬화제에 의한 유전독성을 활성대사억제 및 methylation 억제 , DNA binding 억제 등의 기전으로 감소시키고 있는 것으로 판단되었다. 한편, 소핵생성억제 효과에서 가장 활성이 좋았던 P2를 NMR과 GC/MS결과, aliphatic ketone류의 혼합물로서 주성분은 분질량 330과 386의 두 개 물질이 함유되어 있는 혼합물이었으며 향후 계속적으로 분리 동정이 필요한 물질이다.

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Room Temperature Catalytic Ozonation of Methyl Ethyl Ketone over Mesoporous MnOx/Al2O3 Catalysts

  • Reddy, Kannapu Hari Prasad;Park, Youna;Song, JiHyeon;Park, Young-Kwon
    • 공업화학
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    • 제32권4호
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    • pp.483-486
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    • 2021
  • Catalytic ozonation of methyl ethyl ketone (MEK) has been examined over mesoporous MnOx/Al2O3 (MA) catalysts developed by a solvent deficient method using two different manganese precursors including manganese chloride (C) and manganese sulfate (S) at room temperature. The maximum catalytic activities of MA with C (MEK removal efficiency and ozone decomposition of 98.4 and 93.7%, respectively) were higher than those of MA with S (MEK removal efficiency and ozone decomposition of 96 and 68%, respectively). Also the catalytic stability of MA with C was much higher than that of MA with S. The physico-chemical properties of catalysts are well correlated with the activity results, which confirmed that fine dispersion of MnOx species with high ratios of Mn3+/Mn4+ and more acid sites are attributed to the higher catalyst stability for the MA-C catalyst.

Vibrational Relaxation and Bond Dissociation in Methylpyrazine on Collision with N2 and O2

  • Young-Jin Yu;Sang Kwon Lee;Jongbaik Ree
    • 대한화학회지
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    • 제67권6호
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    • pp.407-414
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    • 2023
  • The present study uses quasi-classical trajectory procedures to examine the vibrational relaxation and dissociation of the methyl and ring C-H bonds in excited methylpyrazine (MP) during collision with either N2 or O2. The energy-loss (-ΔE) of the excited MP is calculated as the total vibrational energy (ET) of MP is increased in the range of 5,000 to 40,000cm-1. The results indicate that the collision-induced vibrational relaxation of MP is not large, increasing gradually with increasing ET between 5,000 and 30,000 cm-1, but then decreasing with the further increase in ET. In both N2 and O2 collisions, the vibrational relaxation of MP occurs mainly via the vibration-to-translation (V→T) and vibration-to-vibration (V→V) energy transfer pathways, while the vibration-to-rotation (V→R) energy transfer pathway is negligible. In both collision systems, the V→T transfer shows a similar pattern and amount of energy loss in the ET range of 5,000 to 40,000cm-1, whereas the pattern and amount of energy transfer via the V→V pathway differs significantly between two collision systems. The collision-induced dissociation of the C-Hmethyl or C-Hring bond occurs when highly excited MP (65,000-72,000 cm-1) interacts with the ground-state N2 or O2. Here, the dissociation probability is low (10-4-10-1), but increases exponentially with increasing vibrational excitation. This can be interpreted as the intermolecular interaction below ET = 71,000 cm-1. By contrast, the bond dissociation above ET = 71,000 cm-1 is due to the intramolecular energy flow between the excited C-H bonds. The probability of C-Hmethyl dissociation is higher than that of C-Hring dissociation.

Pteridine-$C_7$ Side Chain에서 2-탈아미노화와 2-Methyl기 치환에 따른 Aminopterin 중간체 합성에 관한 연구 (Studied on the Synthesis of the 2-Desamino and 2-Desamino-2-Methyl Analogues of Aminopterin intermediate at Pteridine-$C_7$ Side Chain)

  • 유의경;류성렬
    • 대한화학회지
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    • 제37권1호
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    • pp.131-135
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    • 1993
  • 2-Amino-3-cyano-6-chloromethylpyrazine으로부터 합성한 methotrexate(MTX) 중간 유도체의 모핵인 pteridine ring의 $C_2$-amino 대신 $HCH_3$기, 또는 $nH_2$기로 치환된 화합물 (7a),(7b)와 (7c)를 두 단계에 걸쳐 합성하였다. 출발물질인 dibenzyl 4,4'-dithiobisbenzoate(12)와 2-amino-3-cyano-6-chloromethylpyrazine으로부터 합성한 2-amino-3-cyano-6-[(S-p-carbenzyloxyphenyl)thiomethyl]-pyrazine(14)화합물을 formamidine HCl, acetamidine HCl과 guanidine HCl 등과 각각 반응시켜 cyclization시키고, 이 화합물을 ethanol 용매하에서 0.2N NaOH를 사용한 알칼리 가수분해로 pteroic acid유도체를 합성하였다.

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원격 플라즈마 중합된 메틸메타크릴레이트 필름의 분광학적 분석 (Spectroscopic Analysis of the Remote-plasma-polymerized Methyl Methacrylate Film)

  • 서문규
    • 공업화학
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    • 제32권1호
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    • pp.49-54
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    • 2021
  • 메틸 메타크릴레이트 분자를 전구체로 사용하여 원격 플라즈마 방식으로 중합체를 합성하는 반응에서 플라즈마 출력, 반응 압력 및 직접-간접 플라즈마 방식이 필름의 성장속도 및 화학결합 구조에 미치는 영향을 조사하였으며, FT-IR, XPS 등 분광학적 분석과 Langmvir 탐침을 사용한 플라즈마 특성 진단 결과와 함께 고찰하였다. 플라즈마 출력과 반응 압력이 증가하면 성장속도가 증가하지만 특정 영역을 넘어서면 식각 효과와 잦은 충돌로 인해 활성화 효율이 낮아져 다시 감소하였다. 중합 필름의 FT-IR과 XPS 분석 결과, 필름 내 탄소/산소 조성비는 플라즈마 출력이 커질수록 증가하였으며, 탄화수소성 C-C 탄소 조성비는 증가하는 반면 에스터성 COO 탄소 조성비는 감소하였다. 직접 플라즈마법이 간접 플라즈마법에 비해 필름의 성장속도는 2~5배 빠르지만, 전구체의 분자 구조를 유지하기 위해서는 간접 플라즈마법이 유리함을 확인하였다.

작약 잎과 줄기의 건조 방법에 따른 Phenol 화합물의 변화 (Changes of Phenolic Compounds Affected by Different Drying Method in Leaves and Stems of Peony (Paeonia lactiflora Pall.))

  • 김세종;박준홍;최성용;김길웅
    • 한국작물학회지
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    • 제51권spc1호
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    • pp.251-254
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    • 2006
  • 작약의 지상부인 잎과 줄기 부위가 함유하고 있는 주요성분인 paeoniflorin, methyl gallate, astragalin, kaempferol 등 4종의 화합물의 이용성을 높이기 위해 건조방법 및 건조 온도별 성분의 함량 변화를 검토한 결과를 요약하면 다음과 같다. 1. 건조방법별 성분 변화는 kaempferol, methyl gallate, astragalin, paeoniflorin 등 모든 성분은 열풍건조나 dry oven 보다도 원적외선 건조 또는 상온 음건에서 더 높았다. 특히 methyl gallate는 상온 음건에서 0.52%로서 가장 높았다. 2. 건조온도별 성분변화는 kaempferol, methyl gallate, astragalin, paeoniflorin 등은 $40^{\circ}C$ 건조에서는 성분의 함량이 모두 높게 나타났으나 건조온도가 높아질수록 성분은 감소하는 경향이었다.

무용매 , 무유화제 공정에 의한 메틸프룩토시드 올레산 폴리에스테르의 합성 (Solvent-free, Soap-free Synthesis Process of Methyl Fructoside Oleic Acid Polyester)

  • 허주형;김종태;김해성
    • 한국응용과학기술학회지
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    • 제15권4호
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    • pp.45-56
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    • 1998
  • Methyl fructoside oleic acid polyester(MFPE), fructose-based sugar polyester, was synthesized by solvent-free, soap-free transesterification of methyl oleate with methyl fructoside(MF) as a sugar starting material in the presence of conventional potassium carbonate basic catalyst. Methyl fructoside was found to be an effective sugar starting material, because of its low softning point, high heat stability, high miscibility, and high reactivity than other sugars. Yield 98% of purified MFPE based on initial weight of MF was obtained at 1:5 of the molar ratio of methyl fructoside to methyl oleate, 2%(w/w) of potassium carbonate catalyst content, 20${\sim}$200mmHg of reduced pressure and $180^{\circ}C$ of reaction temperature. MFPE structure was confirmed by infrared and proton nuclear magnetic resonance spectroscopy. Physical properties of methyl of fructoside oleic acid polyester such as viscosity, HLB, solubility, color, refractive index, specific gravity, and density were similar to physical properties of sucrose polyesters(SPE) and vegetable oils. Then, it was elucidated that MFPE was sufficient to replace the SPE and conventional oils.

새로운 베타락탐 항생물질의 합성과 생물활성에 관한 연구 (Studies on the Synthesis and Antibacterial Activity of New $\beta$-Lactam Antibiotics)

  • 송태흥;김영호
    • 대한화학회지
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    • 제36권2호
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    • pp.293-300
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    • 1992
  • 신규 cephalosporin계 항생제로서, 7-[(Z)-2-(2-aminothiazol-4-yl)-2-oxyiminoacetamido]-3-(4,6-diamino-1-alkyl-1,3,5-triazinium-2-yl)thiomethyl-3-cephem-4-carboxylate의 유도체들을 합성하였다. 7-위치의 side chain에 있는 oxyimino 부위를 변화시켜서, 구조 변화에 따른 항균 활성의 변화를 측정하였다. 그 결과, 3-위치에서 4,6-diamino-1-methyl-1,3,5-triazinium-2-yl group을 가지며, 또한 7-$\alpha$-methoxyimino기를 가진, C-1유도체가 가장 강력하고도 광범위한 항균활성을 그람 양성과 그람 음성 bacteria에 대하여 나타내었다.

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Synthesis and Photocatalytic Activity of TiO2-ZrO2 Nano-Sized Powders by Sol-Gel Process

  • Han, Jae-Kil;Saito Fumio;Park, Jong-Gu;Lee, Byong-Taek
    • 한국세라믹학회지
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    • 제42권1호
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    • pp.7-10
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    • 2005
  • [ $TiO_{2}-ZrO_{2}$ ] powders were successfully synthesized by the sol-gel process using titanium iso-propoxide as a precursor. The amorphous $TiO_{2}$ particles, 70 nm in size, homogenously adhered to the surface of $ZrO_{2}$ the powders. After calcination at $450^{circ}C$, most of the $TiO_{2}$ powders appeared as an anatase type, whereas they changed to a rutile phase at $750^{circ}C$. For comparison of photocata­lytic activity, $TiO_{2}-ZrO_{2}$ nano-sized powders calcined at $450^{circ}C,\;600^{circ}C,\;and\;750^{circ}C$ were used. In the $TiO_{2}-20wt\%$ $ZrO_{2}$ powders cal­cined at $450^{circ}C$, there was excellent removal efficiency of Methyl Orange (MO). For the calcination temperature increased, $TiO_{2}­ZrO_{2}$ nano-sized powders increased $ZrO_{2}$ contents showed the good photoactivity for the photooxidation of MO.