• 제목/요약/키워드: lactone

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The constituents of taraxacum hallaisanensis roots

  • Yang, Deuk-Suk;Whang, Wan-Kyunn;Kim, Il-Hyuk
    • Archives of Pharmacal Research
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    • 제19권6호
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    • pp.507-513
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    • 1996
  • Three sesquiterpene lactone compounds, two novel(1.betha.,3.betha.-dihydroxy-6.betha.,11.betha.,4.alpha.,5.alpha.,7.alpha.H -eudesm-12, 6-olide-1-O-.betha.-D-glucopyranoside, 1.betha.,3.betha.-dihydroxy-6.betha.,11.betha.,4.alpha.,5.alpha.,7.alpha.H-eudes m-12,6-olide-1-O-.betha.-D-glucopyranoside) and 1.betha.,3.betha.-dihydroxy-6.betha.,11.betha.,4.alpha.,5.alpha., 7.alpha.H-eudesm-12,6-olide were isolated from the aqueous fraction of MeOH extract of the roots from Taraxacum hallaisanensis (Compositae) employing Amberlite XAD-2, ODS-gel, silica gel and Sephadex LH-20 column chromatographics. Another known compound, (-)-epicatechin, was isolated from the aqueous fraction of the MeOH extract. The total MeOH extract also contained phytosterol and a mixture of .betha.-amyrin acetate, .alpha.-amyrin acetate and lupeol acetate. Structures of isolated compounds were elucidated by spectroscopic parameters of IR, Mass, /sup 13/C-NMR, /sup 1/H-NMR, /sup 1/H-/sup 1/H COSY, /sup 13/C-/sup 1/H COSY and HMBC.

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Synthesis and antitumor evaluation of $\alphamethylene-\gamma-butyrolactone-linked$ to 5-substituted uracil nucleic acid bases

  • Kim, Jack-C.;Kim, Ji-A;Kim, Si-Hwan;Park, Jin-Il;Kim, Seon-Hee;Park, Soon-Kyu;Park, Won-Woo
    • Archives of Pharmacal Research
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    • 제19권3호
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    • pp.235-239
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    • 1996
  • Six, heretofore undescribed, $5^I-Methyl-5^I-(5-Substituted uracil-1-ylmethyl)-2^I-oxo-3^I-methylenetetrahydrofurans(F, Cl, Br, l, CH_3, H)(6a-f)$were synthesized and evaluated against three cell lines (FM-3A, P-388 and U-937). For the preparation of .alpha.-methylene-.gamma.-butyrolactone bearing 5-substituted uracils (6a-f), the effcient Reformatsky type reaction was employed which involves the treatment of ethyl .alpha.(bromomethyl) acrylate and zinc with the respective 5-substituted uracil-1-ylacetones (5a-f). The acetone derivatives (5a-f) were directly obtained by the respective alkylation reaction of 5-substituted uracils with chloroacetone in the presence of $K_{2}$$CO_{3}$(or NaH). These lactone compounds 6a-f exhibited moderate to significant activity in all of the three cell lines, and 6b, 6c and 6e showed significant antitumor activities (inhibitory concentrations ($IC_{50}$) ranged from 1.3-3.8 .mu.g/ml.

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Role of LuxIR Homologue AnoIR in Acinetobacter nosocomialis and the Effect of Virstatin on the Expression of anoR Gene

  • Oh, Man Hwan;Choi, Chul Hee
    • Journal of Microbiology and Biotechnology
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    • 제25권8호
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    • pp.1390-1400
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    • 2015
  • Quorum sensing is a process of cell-to-cell communication in which bacteria produce autoinducers as signaling molecules to sense cell density and coordinate gene expression. In the present study, a LuxI-type synthase, AnoI, and a LuxR-type regulator, AnoR, were identified in Acinetobacter nosocomialis, an important nosocomial pathogen, by sequence analysis of the bacterial genome. We found that N-(3-hydroxy-dodecanoyl)- L -homoserine lactone (OH-dDHL) is a quorum-sensing signal in A. nosocomialis. The anoI gene deletion was responsible for the impairment in the production of OH-dDHL. The expression of anoI was almost abolished in the anoR mutant. These results indicate that AnoI is essential for the production of OH-dDHL in A. nosocomialis, and its expression is positively regulated by AnoR. Moreover, the anoR mutant exhibited deficiency in biofilm formation. In particular, motility of the anoR mutant was consistently and significantly abolished compared with that of the wild type. The deficiency in the biofilm formation and motility of the anoR mutant was significantly restored by a functional anoR, indicating that AnoR plays important roles in the biofilm formation and motility. Furthermore, the present study showed that virstatin exerts its effects on the reduction of biofilm formation and motility by inhibiting the expression of anoR. Consequently, the combined results suggest that AnoIR is a quorum-sensing system that plays important roles in the biofilm formation and motility of A. nosocomialis, and virstatin is an inhibitor of the expression of anoR.

Bryostatin-1에 의한 Wnt/${\beta}$-Catenin 신호전달체계 저해효과 (Suppression of the Wnt/${\beta}$-catenin Pathway by Bryostatin-1)

  • 박서영;오상택
    • 한국미생물·생명공학회지
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    • 제42권1호
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    • pp.89-92
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    • 2014
  • Wnt/${\beta}$-catenin 신호전달체계는 세포 증식, 분화, 그리고 기관 발생과 같은 다양한 생명현상에 중요한 역할을 한다. 본 연구에서는 세포기반 스크리닝 기법을 사용하여 Wnt/${\beta}$-catenin 신호전달체계를 저해하는 bryostatin-1을 발굴하였다. Bryostain 1은 ${\beta}$-catenin의 mRNA 수준에는 영향을 미치지 않는 반면 세포 내 ${\beta}$-catenin 단백질 수준을 감소시킴으로 Wnt3a-CM에 의해 활성화 된 ${\beta}$-catenin response transcription (CRT)을 억제하였다. 또한 프로테아좀의 활성을 저해하였을 경우 bryostatin-1에 의한 ${\beta}$-catenin 수준 감소가 억제되었다. 본 연구의 결과들로부터 bryostatin-1이 프로테아좀에 의한 ${\beta}$-catenin 단백질 분해를 촉진함으로써 Wnt/${\beta}$-catenin 신호전달체계를 저해함을 확인하였다.

두릅의 휘발성 향기성분에 관한 연구 (Volatile Compounds Isolated from Edible Korean Fatsia Shoots (Aralia elata Seem.))

  • 김소미;정태영
    • Applied Biological Chemistry
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    • 제39권5호
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    • pp.389-397
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    • 1996
  • 연속수증기증류장치를 이용하여 두릅으로부터 얻어진 휘발성농축물은 탄화수소구분 및 함산소구분으로 분리되었고, 함산소구분은 실리카겔 관 크로마토그래피에 의해서 9개의 계대구분으로 다시 분획하였다. 기체크로마토그래피와 기체크로마토그래피에 질량분석계를 연결시킨 장치는 휘발성성분을 동정하기 위하여 사용하였다. 동정된 167개의 휘발성성분은 72개의 탄화수소, 31개의 알콜, 23개의 알데히드, 16개의 에스테르, 10개의 산, 6개의 케톤, 3개의 푸론, 2개의 페놀, 1개의 인돌, 1개의 산화물, 1개의 설파이드 및 1개의 락톤이었다. Sesquiterpene 탄화수소인 ${\beta}-caryopyllene$은 두릅에서 동정된 휘발성 성분중에서 함량이 가장 높았으며, 19.53%를 차지하였다. 두릅정유는 관능검사용 기체크로마토그래피를 사용하여 각 구분에 함유된 개별 휘발성성분을 평가에 의해서 초목 모양의 향기를 함유하고 있음이 밝혀졌다.

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가공조건이 alginate 필름의 물리적성질에 미치는 영향 (Effects of processing conditions on physical properties of alginate film)

  • 유병진;심재만
    • 한국수산과학회지
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    • 제32권5호
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    • pp.582-586
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    • 1999
  • 생분해성으로서 가식성인 alginate 필름을 가공하기 위한 기초자료로써 $3\%$ $Na_2CO_3$ 추출시간 5시간으로 추출한 alginate로 만든 alginate 필름의 수증기 투과율과 장력성에 영향을 미치는 alginate농도와 가소제의 종류별 첨가량에 관한 조건을 측정한 결과는 다음과 같다. Alginate의 농도가 증가할수록 인장강도는 증가하였으나 수증기 투과율과 신장도는 감소하였다. 반면에 가소제의 첨가량이 증가할수록 수증기 투과율과 신장도는 증가하였으나 인장강도는 감소하였다. 가소제의 종류별에 따른 수증기 투과율은 glycerol, polyethylene glycol 및 sorbitol 첨가 필름 순으로 높게 나타났으며, 인장강도는 polyethylene glycol, sorbitol, glycerol 첨가 필름 순서이었으나 신장도는 그 반대되는 결과였다. 가소제의 종류와 필름의 색은 sorbitol 첨가 필름의 색이 가장 자았고, 황색도는 glycerol 첨가 필름이 가장 높았고, 적색도는 polyethylene glycol 첨가 필름이 가장 높았다. 그리고 전체적인 색의 차이에서는 polyethylene glycol 첨가 필름이 가장 높았다.

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Hemistepsin A inhibits T0901317-induced lipogenesis in the liver

  • Kim, Jae Kwang;Cho, Il Je;Kim, Eun Ok;Lee, Dae Geon;Jung, Dae Hwa;Ki, Sung Hwan;Ku, Sae Kwang;Kim, Sang Chan
    • BMB Reports
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    • 제54권2호
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    • pp.106-111
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    • 2021
  • Hemistepsin A (HsA) is a guaianolide sesquiterpene lactone that inhibits hepatitis and liver fibrosis. We evaluated the effects of HsA on liver X receptor (LXR)-mediated hepatic lipogenesis in vitro and in vivo. Up to 10 μM, HsA did not affect the viability of HepG2 and Huh7 cells. Pretreatment with 5-10 μM HsA significantly decreased the luciferase activity of the LXR response element, which was transactivated by T0901317, GW 3965, and LXRα/retinoid X receptor α overexpression. In addition, it significantly inhibited the mRNA expression of LXRα in HepG2 and Huh7 cells. It also suppressed the expression of sterol regulatory element-binding protein-1c and lipogenic genes and reduced the triglyceride accumulation triggered by T0901317. Intraperitoneal injection of HsA (5 and 10 mg/kg) in mice significantly alleviated the T0901317-mediated increases in hepatocyte diameter and the percentage of regions in hepatic parenchyma occupied by lipid droplets. Furthermore, HsA significantly attenuated hepatic triglyceride accumulation by restoring the impaired expression of LXRα-dependent lipogenic genes caused by T0901317. Therefore, based on its inhibition of the LXRα-dependent signaling pathway, HsA has prophylactic potential for steatosis.

Reaction of Sodium Diethyldihydroaluminate with Selected Organic Compounds Containing Representative Functional Groups

  • Yoon Nung Min;Shon Young Seok;Ahn Jin Hee
    • Bulletin of the Korean Chemical Society
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    • 제13권2호
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    • pp.199-207
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    • 1992
  • The approximate rates and stoichiometry of the reaction of excess sodium diethyldihydroaluminate (SDDA) with 68 selected organic compounds containing representative functional groups were examined under standard conditions (THF-toluene, $0^{\circ}C$ in order to compare its reducing characteristics with lithium aluminum hydride (LAH), aluminum hydride, and diisobutylaluminum hydride (DIBAH) previously examined, and enlarge the scope of its applicability as a reducing agent. Alcohols, phenol, thiols and amines evolve hydrogen rapidly and quantitatively. Aldehydes and ketones of diverse structure are reduced rapidly to the corresponding alcohols. Reduction of norcamphor gives 11% exo-and 89% endo-norborneol. Conjugated aldehydes such as cinnamaldehyde are rapidly and cleanly reduced to the corresponding allylic alcohols. p-Benzoquinone is mainly reduced to hydroquinone. Hexanoic acid and benzoic acid liberate hydrogen rapidly and quantitatively, however reduction proceeds very slowly. Acid chlorides and esters tested are all reduced rapidly to the corresponding alcohols. However cyclic acid anhydrides such as succinic anhydride are reduced to the lactone stage rapidly, but very slowly thereafter. Although alkyl chlorides are reduced very slowly alkyl bromides, alkyl iodides and epoxides are reduced rapidly with an uptake of 1 equiv of hydride. Styrene oxide is reduced to give 1-phenylethanol quantitatively. Primary amides are reduced very slowly; however, tertiary amides take up 1 equiv of hydride rapidly. Tertiary amides could be reduced to the corresponding aldehydes in very good yield ( > 90%) by reacting with equimolar SDDA at room temperature. Hexanenitrile is reduced moderately accompanying 0.6 equiv of hydrogen evolution, however the reduction of benzonitrile proceeds rapidly to the imine stage and very slowly thereafter. Benzonitrile was reduced to give 90% yield of benzaldehyde by reaction with 1.1 equiv of hydride. Nitro compounds, azobenzene and azoxybenzene are reduced moderately at $0^{\circ}C$, but nitrobenzene is rapidly reduced to hydrazobenzene stage at room temperature. Cyclohexanone oxime is reduced to the hydroxylamine stage in 12 h and no further reaction is apparent. Pyridine is reduced sluggishly at $0^{\circ}C$, but moderately at room temperature to 1,2-dihydropyridine stage in 6 h; however further reaction is very slow. Disulfides and sulfoxides are reduced rapidly, whereas sulfide, sulfone, sulfonic acid and sulfonate are inert under these reaction conditions.

Development of Hydrophobically Modified Casein Derivative-Based Delivery System for Docosahexaenoic Acids by an Acid-Induced Gelation

  • Ho-Kyung Ha;Dan-Bi Woo;Mee-Ryung Lee;Won-Jae Lee
    • 한국축산식품학회지
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    • 제43권2호
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    • pp.220-231
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    • 2023
  • Although omega-3 fatty acids including docosahexaenoic acid (DHA) contain various health-promoting effects, their poor aqueous solubility and stability make them difficult to be induced in dairy foods. The aims of this research were to manufacture casein derivative-based delivery system using acid-induced gelation method with glucono-σ-lactone and to investigate the effects of production variables, such as pH and charged amount of linoleic acid, on the physicochemical properties of delivery systems and oxidative stability of DHA during storage in model milk. Covalent modification with linoleic acid resulted in the production of casein derivatives with varying degrees of modification. As pH was reduced from 5.0 to 4.8 and the charged amount of linoleic acid was increased from 0% to 30%, an increase in particle size of casein derivative-based delivery systems was observed. The encapsulation efficiency of DHA was increased with decreased pH and increased charged amount of linoleic acid. The use of delivery system for DHA resulted in a decrease in the development of primary and secondary oxidation products. An increase in the degree of modification of casein derivatives with linoleic acid resulted in a decrease in the formation of primary and secondary oxidation products than of free DHA indicating that delivery systems could enhance the oxidative stability of DHA during storage in model milk. In conclusions, casein derivatives can be an effective delivery system for DHA and charged amount of linoleic acid played a key role determining the physicochemical characteristics of delivery system and oxidative stability of DHA.

Chemical Composition and Quorum Sensing Inhibitory Effect of Nepeta curviflora Methanolic Extract against ESBL Pseudomonas aeruginosa

  • Haitham Qaralleh
    • 대한약침학회지
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    • 제26권4호
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    • pp.307-318
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    • 2023
  • Objectives: Bacterial biofilm is regarded as a significant threat to the production of safe food and the arise of antibiotic-resistant bacteria. The objective of this investigation is to evaluate the quorum sensing inhibitory effect of Nepeta curviflora methanolic extract. Methods: The effectiveness of the leaves at sub-inhibitory concentrations of 2.5, 1.25, and 0.6 mg/mL on the virulence factors and biofilm formation of P. aeruginosa was evaluated. The effect of N. curviflora methanolic extract on the virulence factors of P. aeruginosa, including pyocyanin, rhamnolipid, protease, and chitinase, was evaluated. Other tests including the crystal violet assay, scanning electron microscopy (SEM), swarming motility, aggregation ability, hydrophobicity and exopolysaccharide production were conducted to assess the effect of the extract on the formation of biofilm. Insight into the mode of antiquorum sensing action was evaluated by examining the effect of the extract on the activity of N-Acyl homoserine lactone (AHL) and the expression of pslA and pelA genes. Results: The results showed a significant attenuation in the production of pyocyanin and rhamnolipid and in the activities of protease and chitinase enzymes at 2.5 and 1.25 mg/mL. In addition, N. curviflora methanolic extract significantly inhibited the formation of P. aeruginosa biofilm by decreasing aggregation, hydrophobicity, and swarming motility as well as the production of exopolysaccharide (EPS). A significant reduction in AHL secretion and pslA gene expression was observed, indicating that the extract inhibited quorum sensing by disrupting the quorum-sensing systems. The quorum-sensing inhibitory effect of N. curviflora extract appears to be attributed to the presence of kaempferol, quercetin, salicylic acid, rutin, and rosmarinic acid, as indicated by LCMS analysis. Conclusion: The results of the present study provide insight into the potential of developing anti-quorum sensing agents using the extract and the identified compounds to treat infections resulting from quorum sensing-mediated bacterial pathogenesis.