• 제목/요약/키워드: Acetophenone

검색결과 102건 처리시간 0.029초

산해박 뿌리에서 추출한 정유 및 구성성분의 인간 장내미생물에 대한 항균활성 및 작은소피참진드기에 대한 살비활성 (Acaricidal and antimicrobial toxicities of Cyanachum paniculatum root oils and these components against Haemaphysalis longicornis and human intestinal bacteria)

  • 이명지;김희주;정아현;이회선
    • Journal of Applied Biological Chemistry
    • /
    • 제61권4호
    • /
    • pp.423-428
    • /
    • 2018
  • 산해박 뿌리 정유 추출물에 대한 장내 미생물 5종(Bifidobacterium bifidum, B. longum, C. perfringens, E. coli 및 L. casei)의 항균활성 및 작은소피참진드기(Haemaphysalis longicornis)의 살비활성을 검정하였다. 산해박 정유는 20.0 mg/disc에서 유해균 2종(C. perfringens 및 E. coli)에 대해 항균활성을 확인하였으나, 작은소피참진드기에는 살비활성을 나타내지 않았다. GC-MS 분석을 통해 얻어진 구성성분 중에 2'-hydroxy-5'-methoxyacetophenone이 유해균 2종에 대해서 10.0 mg/disc에서 각각 12.1 및 12.0 mm의 inhibition zone이 나타난 것을 확인하였다. 이와 같은 결과로 인하여 2'-hydroxy-5'-methoxyacetophenone 유도 화합물들의 구조에 따른 항균활성을 검정하고자 acetophenone 계열 유도체 10종(acetophenone, 2'-hydroxyacetophenone, 4'-hydroxyacetophenone, 2'-methoxyacetophenone, 4'-methoxyacetophenone, 2',4'-dihydroxyacetophenone, 2',5'-dihydroxyacetophenone, 2',4'-dimethoxyacetophenone, 2',5'-dimethoxyacetophenone 및 2'-hydroxy-4'-methoxyacetophenone)과 비교 실험한 결과, methyl group이 포함된 acetophenone 유도화합물에서는 유해균 2종에 대해 항균활성을 나타내었으며, 장내유익균에 대해서는 영향을 미치지 않았다. 그러나 hydroxyl group이 포함된 acetophenone 유도화합물에서는 장내 미생물에 대해 항균 활성이 전혀 나타내지 않았다. 이상의 결과를 통해 산해박 정유와 구성성분 2'-hydroxy-5'-methoxyacetophenone 및 그 유도체는 천연 장내 세균총 개선제로서의 가능성을 제시하였다.

Cynanchum wilfordii의 성분함량 분석 (Quantitative analysis of Cynanchum wilfordii Hemsley)

  • 이혜원;박소영;이아영;채성욱;최고야;추병길;김호경
    • 한국한의학연구원논문집
    • /
    • 제14권1호
    • /
    • pp.107-111
    • /
    • 2008
  • Objectives : Cynanchum wilfordii(Asclepiadaceae) has been traditionally used as a tonic, the prevention and treatment of various geriatric diseases in Korea. Acetophenone derivatives from C. wilfordii showed neuroprotective activity. In this study, two acetophenones were isolated and quantitative determination of acetophenones from C. wilfordii has been developed for quality stand. Methods : Three acetophenone derivatives were isolated from methanol extract of C. willfordii by the chromatographic separation. Their structures were identified as cynandione A, 2,5-dihydroxy acetophenone and cynanchone A on the basis of spectral data(MS, $^1H-NMR$, $^{13}C-NMR$) and chemical analysis. HPLC analysis was performed to determine the contents of cynandione A and 2,5-dihydroxyacetophenone in C. wilfordii. Results : According to the results, the contents of cynandione A and 2,5- dihydroxyacetophenone were 0.274%, 0.035% by HPLC, respectively. Conclusions : In these results, we have determined the contents of cynandione A and 2,5-dihydroxyacetophenone in Cynanchum wilfordii, respectively. We hope that this study will contribute to the standardization and quality control of herbal medicine.

  • PDF

수소화붕소리튬, 보란 및 보란-염화리튬 (1 : 0.1)에 의한 카르보닐화합물의 선택환원 (Selective Reduction of Carbonyl Compounds with Lithium Borohydride, Borane, and Borane-Lithium Chloride (1 : 0.1) in Tetrahydrofuran)

  • 윤능민;차진순
    • 대한화학회지
    • /
    • 제22권4호
    • /
    • pp.259-267
    • /
    • 1978
  • 수소화붕소리튬, 보란 그리고 보란-염화리튬(1:0.1)의 카르보닐화합물 환원에 있어서의 선택성을 5쌍의 대표적인 카르보닐화합물 쌍(벤즈알데히드-아세토페논, 벤즈알데히드-2-헵탄온, 2-헵탄온-벤조페논, 아세토페논-벤조페논, 2-헵탄온-아세토페논)에 대해서 이들 수소화물의 제한된 양을 반응시켜 알아보았다. 이들 수소화물중 보란-염화리튬(1:0.1)이 제일 선택성이 좋았고, 수소화붕소 리튬과 보란도 2-헵탄온-아세토페논 쌍을 제외하고는 좋은 선택성을 보였다.

  • PDF

밤꽃의 휘발성 화합물 특성 (Volatile Components of Chestnut (Castanea crenata Sieb. et Zucc.) Flower)

  • 김연순;박은령;김경수
    • 한국식품영양과학회지
    • /
    • 제32권6호
    • /
    • pp.801-805
    • /
    • 2003
  • 밤꿀의 밀원이 되는 밤꽃에서 SDE 추출법과 GC-FID 및 GC/MS 분석방법으로 122종의 휘 발성 성분을 분리ㆍ동정하였다. 밤꽃의 휘발성분 조성은 전체 향기성분 중 alcohol류가 36.58%로 가장 높은 함량을 보였으며, 그 다음으로 15종의 hydrocarbon류, 20종의 terpene류와 유도체, 7종의 ketone류,24종의 aldehyde류, 12종의 ester류, 4종의 acid류, 3종의 furan류와 2종의 기타 화합물 순으로 구성되어 있음이 확인되었다. 밤꽃 휘발성분의 주성분은 전 체 peak area의 18.6%을 구성하는 1-phenylethanol과 (E)-geraniol, tricosane, heneicosane, benzyl alcohol, acetophenone, 2-phenylethanol 등으로 방향족 alcohol과 홀수탄소로 구성 된 포화탄화수소들이었다. 밤꽃 추출물의 휘발성분에는 밤꿀의 밀원을 판단할 수 있게끔 하는 marker로써 사용가능성을 지닌 1-phenyl-ethanol과 acetophenone이 주성분으로 구성되어있으며, 밤꽃의 특징적인 강한 동물취와 꽃향이 혼합된 형태의 향 특성은 nonanal 등에 기인한다고 판단되었다.

Efficient Enantioselective Synthesis of (R)-[3,5-Bis(trifluoromethyl)phenyl] Ethanol by Leifsonia xyli CCTCC M 2010241 Using Isopropanol as Co- Substrate

  • Ouyang, Qi;Wang, Pu;Huang, Jin;Cai, Jinbo;He, Junyao
    • Journal of Microbiology and Biotechnology
    • /
    • 제23권3호
    • /
    • pp.343-350
    • /
    • 2013
  • (R)-[3,5-Bis(trifluoromethyl)phenyl] ethanol is a key chiral intermediate for the synthesis of aprepitant. In this paper, an efficient synthetic process for (R)-[3,5- bis(trifluoromethyl)phenyl] ethanol was developed via the asymmetric reduction of 3,5-bis(trifluoromethyl) acetophenone, catalyzed by Leifsonia xyli CCTCC M 2010241 cells using isopropanol as the co-substrate for cofactor recycling. Firstly, the substrate and product solubility and cell membrane permeability of biocatalysts were evaluated with different co-substrate additions into the reaction system, in which isopropanol manifested as the best hydrogen donor of coupled NADH regeneration during the bioreduction of 3,5-bis(trifluoromethyl) acetophenone. Subsequently, the optimization of parameters for the bioreduction were undertaken to improve the effectiveness of the process. The determined efficient reaction system contained 200mM of 3,5-bis(trifluoromethyl) acetophenone, 20% (v/v) of isopropanol, and 300 g/l of wet cells. The bioreduction was executed at $30^{\circ}C$ and 200 rpm for 30 h, and 91.8% of product yield with 99.9% of enantiometric excess (e.e.) was obtained. The established bioreduction reaction system could tolerate higher substrate concentrations of 3,5- bis(trifluoromethyl) acetophenone, and afforded a satisfactory yield and excellent product e.e. for the desired (R)-chiral alcohol, thus providing an alternative to the chemical synthesis of (R)-[3,5-bis(trifluoromethyl)phenyl] ethanol.

아세토페논이 양모의 염색속도에 미치는 영향 (Effect of Acetophenone on the Rate of Wool Dyeing)

  • 도성국
    • 한국의류산업학회지
    • /
    • 제10권3호
    • /
    • pp.394-398
    • /
    • 2008
  • One of barely water soluble ketones, acetophenone (AP) was dissolved in methanol and then was mixed with aqueous solution of C. I. Red Acid 114. In order to find out the role of AP in the dyeing process the rate constants and the activation parameters were calculated. The rate for the dyeing with AP was faster than that without it. Because of the reduced temperature dependence by AP the activation energy ($E_a$) for the dyeing with AP was smaller than that without it. With increasing temperature the activation enthalpy (${\Delta}H^*$), the activation entropy (${\Delta}S^*$), and the activation free energy ($G^*$) decreased, which was more noticeable in dyeing with AP. The rate constants and the activation parameters agreed well with the results from the previous reports that the ability of AP to increase disaggregation of dye molecules, loosening the wool fiber, and wickabilty of dyeing solution made it possible to dye wool fiber at low temperature.

GC-Mass에 의한 만삼(蔓蔘) 에텔엑기스의 성분 연구 (Studies on the Components of Codonopsis pilosulae Radix by GC-Mass)

  • 이인란
    • 생약학회지
    • /
    • 제16권3호
    • /
    • pp.136-140
    • /
    • 1985
  • Sixty-eight kinds of aliphatic and aromatic substances peaks from ether extract of Codonopsis pilosulae Radix were shown by GC-Mass. Of them, 3 kinds of compounds were identified as ethyl benzene, acetophenone and 1-phenyl-2-butanone, which are compared with authentic specimen, and one compound was assumed as an aliphatic $C_8H_{16}O\;or\;C_9H_{20}$.

  • PDF

양모의 저온 염색(1) - 용해도 파라미터$(\delta)$를 중심으로 - (Dyeing of Wool at Low Temperature - focusing on solubility parameter$(\delta)$ -)

  • 도성국
    • 한국염색가공학회지
    • /
    • 제15권6호
    • /
    • pp.55-62
    • /
    • 2003
  • Wool fabrics were dyed with the aqueous solution of C. I. Red Acid 114 mixed with methanol dissolving three kinds of barely water soluble ketones, acetophenone, 2-pentanone, and 3-pentanone. The steric hinderance and the orientation of the bigger hydrophobic part of the solvated dye molecules to the fiber slowed down the dying rate, however, loosening the wool molecule, say a little swelling, disaggeregating the dye molecules, and attaining the higher dye concentration on the fiber surface by the added solvents increased the amount of dye on the fabric. The higher concentration or/and the higher dyeing temperature helped loosen fiber molecules and made it easier for the solvated dye molecules to penetrate into the inside of the fiber. Acetophenone, the most influential solvent used, showed that the ability to loosen fiber molecules was the most important of all the three positive solvent actions mentioned above. The considered mechanism provided before reflected the fact that the dye uptake on the fabric dyed with the solvents included, except for 0.034M and 0.051M of acetophenone, was even lower than that without any solvents at $50^\circ{C}$, but all the solvents added to the dye bath increased the dye uptake on the fiber at $70^\circ{C}$.

An Acetophenone Derivative, Clavatol, and a Benzodiazepine Alkaloid, Circumdatin A, from the Marine-Derived Fungus Cladosporium

  • Yang, Guohua;Nenkep, Viviane N.;Siwe, Xavier N.;Leutou, Alain S.;Feng, Zhile;Zhang, Dahai;Choi, Hong-Dae;Kang, Jung-Sook;Son, Byeng-Wha
    • Natural Product Sciences
    • /
    • 제15권3호
    • /
    • pp.130-133
    • /
    • 2009
  • The crude extract of the mycelium of Cladosporium was found to exhibit antimicrobial activity against the Staphylococcus aureus, methicillin-resistant S. aureus, and multidrug-resistant S. aureus. Bioassayguided fractionation of an organic extract led to the isolation of an acetophenone derivative, clavatol (2',4'-dihydroxy-3',5'-dimethylacetophenone) (1), and a benzodiazepine alkaloid, circumdatin A (2). Compound 1 showed moderate antibacterial activity against S. aureus, methicillin-resistant S. aureus, and multidrug-resistant S. aureus with minimum inhibitory concentration (MIC) values of 62.5, 62.5, 31.0 $\mu$g/mL, respectively, but compound 2 was inactive. Compounds 1 and 2 exhibited UV-A protection activity with ED$_{50}$ values of 227.0 and 82.0 $\mu$M, respectively, indicating that they were more potent than the positive control, oxybenzone (ED$_{50}$ 350 $\mu$M), a common sunscreen agent.

Novel solvothermal approach to hydrophilic nanoparticles of late transition elements and its evaluation by nanoparticle tracking analysis

  • Dutilleul, Marion Collart;Seisenbaeva, Gulaim A.;Kessler, Vadim G.
    • Advances in nano research
    • /
    • 제2권2호
    • /
    • pp.77-88
    • /
    • 2014
  • Solvothermal treatment of late transition metal acetylacetonates in a novel medium composed either of pure acetophenone or acetophenone mixtures with amino alcohols offers a general approach to uniform hydrophilic metal nanoparticles with high crystallinity and low degree of aggregation. Both pure metal and mixed-metal particles can be accesses by this approach. The produced materials have been characterized by SEM-EDS, TEM, FTIR in the solid state and by Nanoparticle Tracking Analysis in solutions. The chemical mechanisms of the reactions producing nanoparticles has been followed by NMR. Carrying out the process in pure acetophenone produces palladium metal, copper metal with minor impurity of $Cu_2O$, and NiO. The synthesis starting from the mixtures of Pd and Ni acetylacetonates with up to 20 mol% of Pd, renders in minor yield the palladium-based metal alloy along with nickel oxide as the major phase. Even the synthesis starting from a mixed solution of $Cu(acac)_2$ and $Ni(acac)_2$ produces oxides as major products. The situation is improved when aminoalcohols such as 2-aminoethanol or 2-dimethylamino propanol are added to the synthesis medium. The particles in this case contain metallic elements and pairs of individual metals (not metal alloys) when produced from mixed precursor solutions in this case.