• 제목/요약/키워드: Methyl C(2)

검색결과 1,763건 처리시간 0.028초

Preparation of N'-Substituted Anilino-N-Methyl-N-Nitorsoureas as Candidate Antitumor Agents

  • Kim, Jack-C;Kim, Yeon-Gweon;Min, Byoung-Tack;Park, Jin-Il
    • Archives of Pharmacal Research
    • /
    • 제17권6호
    • /
    • pp.420-423
    • /
    • 1994
  • Various N'-substituted anilino-N-methyl-N'-nitrosoureas(2a-n) were easily prepared from the reaction of substituted phenylhydraines $(3, 4-CH_3, {\;} 3-, {\;} 4-OCH_3, {\;} 3-, {\;} 4-F, {\;} 3, {\;} 4-Cl, {\;} 4-Br, {\;} 2-, {\;} 3-, {\;} 4-NO_2, 4-(NO_2)_2)$ with methyl isocyanate, followed by the nitrosation with 99% HCOOH and dry sodium lnitrite powder. Surprisingly, of these series of analogus, the anilino-nitrocosureas substituted with eletron-withdrawing nitro groups (2k-a) showed significantly low $ED_{30}$ values of $1.4-3.4 {\mu}g/ml.$ In addition, none of these copounds subtituted with electron-donating groups exhibited cytotoxicities.

  • PDF

감마선과 Methyl Bromide 처리가 사과의 생리화학적 품질에 미치는 영향 (Effects of Gamma Radiation and Methyl Bromide Fumigation on Physiological and Chemical Quality of Apples)

  • 강호진;정헌식;조덕조;변명우;최성진;최종욱;권중호
    • 한국식품저장유통학회지
    • /
    • 제10권3호
    • /
    • pp.381-387
    • /
    • 2003
  • 감마선(0, 0.5, 1, 2, 3 kGy) 조사와 methyl bromide(MeBr, 2 g/kg, 4 hr) 훈증 및 이들의 처리시기가 사과의 생리화학적 품질특성에 미치는 영향을 비교하여, 검역처리를 위한 감마선 조사의 응용성을 검토하였다. 감마선과 MeBr 처리에 따른 사과의 생리화학적 품질평가에서 2 kGy 이상의 감마선 조사와 MeBr 훈증은 사과의 일부 생리화학적 품질특성의 변화를 촉진시키는 것으로 나타났다. 감마선과 MeBr의 처리시기별로는 수확 직후보다는 저온($0^{\circ}C$)에서 40일 정도 보관한 후 처리한 것이 대체적으로 품질손상이 적은 것으로 나타났다. 따라서 1 kGy 이하의 감마선 조사와 지연조사는 사과 과실의 품질을 비교적 양호한 상태로 유지할 수 있어 검역처리 기술로 활용성이 있는 것으로 생각된다.

Ethanol/3-methyl-1-butanol계의 기-액평형치 추산 (The Prediction of Vapor-Liquid Equilibrium Data for Ethanol/3-methyl-1-butanol System)

  • 이준만;이영세
    • 한국산학기술학회:학술대회논문집
    • /
    • 한국산학기술학회 2009년도 춘계학술발표논문집
    • /
    • pp.863-866
    • /
    • 2009
  • Ethanol/3-methyl-1-butanol 계에 대하여 정온하 즉 50, 55, 60, 65, 70, 75 및 $80^{\circ}C$에서 2성분 기-액 평형측정치를 측정하였다. 측정된 기-액평형치의 액조성과 비휘발도의 대수치와의 관계를 직교좌표에 plot하면 직선이 이루어지고 온도변화에 대한 각각의 직선이 평형임을 확인하였다. Ethanol/3-methyl-1-butanol 계에 대한 추산식은 각각의 온도변화에 따라 나타내었고 이식들을 이용하여 추산식을 구하였다. 추산식으로부터 구한 추산치와 측정치를 비교 검토한 결과 Ethanol/3-methyl-1-butanol 계에서는 기상조성의 몰분율은 ${\pm}0.00051$[-]의 오차 범위에서 잘 일치하는 것으로 나타났고, modified UNIFAC방법은 실측치와 비교한 평균오차는 ${\pm}0.0022$[-]에서 추산하였다. 따라서 본 연구에서 제안한 추산법이 2성분계 기-액평형치를 추산하는 방법으로 타당함을 확인하였다.

  • PDF

생쥐의 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine(MPTP)-유도 신경독성에 대한 대황의 보호효과 (Protective Effect of R. palmatum on 1-Methyl-4-phenyl-l,2,3,6-tetrahydropyridine (MPTP)-induced Neurotoxicity in Mice)

  • 이형철;김대근;조원준;황석연;이영구;김명동;전병훈
    • 약학회지
    • /
    • 제46권6호
    • /
    • pp.433-440
    • /
    • 2002
  • The protective efficacy of Rheum palmatum water extract on 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced parkinsonism was studied in C57BL/6 mice. In order to demonstrate neuroprotective effect of R. palmatum extract, animals were administered intraperitoneally with the water extract (100 or 200 mg/kg/day) for 14 days, and MPTP (10 mg/kg/day) was injected subcutaneously into the mice for the first 6 consecutive days from the beginning 1 hr before R. palmatum extract treatment. All animals were measured the several neurobiochemical markers such as dopamine level and monoamine oxidase B (MAO-B) activity in various regions of brain. The treatment of mice with R. palmatum extract was confirmed recovery effect on MAO-B activity in the cerebellum and the cerebral cortex. R. palmatum extract was attenuated the MPTP-induced depletion of substantia nigra dopamine. The contents of MDA, a marker of lipid peroxidation, in brain tissues (cerebellum and cerebral cortex mitochondria) were decreased significantly by R. palmatum extract. These results suggest that R. palmatum water extract plays an effective role in attenuating MPTP-induced neurotoxicity in mice. This protective effect of R. palmatum might be estimated the result from the inhibitory activity on monoamine oxidase B and the enhancement of antioxidant activity.

Solvent-water-2-propanol 삼성분계의 액-액평형 (LLE of Solvent-Water-2-Propanol Ternary Systems)

  • 정상훈;이진우;박동원
    • 공업화학
    • /
    • 제8권4호
    • /
    • pp.653-659
    • /
    • 1997
  • 에너지 비용의 상승에 따라 추출의 기본원리를 둔 새로운 분리공정에 대한 연구가 많이 진행되고 있으며, 이에 따라 액-액평형 조성의 계산 및 예측에 대한 필요성이 매우 증가하고 있다. 본 연구에서는 공비혼합물을 형성하는 2-propanol 수용액에 용매로서 methyl ethyl ketone, methyl isobutyl ketone, ethylacetate, butylacetate, toluene 및 o-xylene을 첨가한 삼성분계에 대하여 $25^{\circ}C$에서 용해도곡선, tie line, plait point, 분배계수와 선택도를 실험을 통해 구하였다. Tie line 데이터의열역학적 건전성을 확인하였으며 실험값을 NRTL 및 UNIQUAC 모델식으로 구한 계산값과 비교하였다.

  • PDF

폴리올류를 친수부로 한 비이온성 계면활성제의 용액거동 (Solution Behaviour of Nonionic Surfactants with Polyolic Group as Hydrophilic Portion)

  • 김상춘;김태영;이승렬;노승호;남기대
    • 공업화학
    • /
    • 제5권4호
    • /
    • pp.573-579
    • /
    • 1994
  • 본 연구에 사용된 비이온성 계면활성제는 1-O-oleoyl glycerol, 2-O-oleoyl-myo-inositol 및 methyl 2-O-oleoyl-${\alpha}$-glucopyranoside였다. 이들 3종류의 비이온성 계면환성제에 대한 용액성질과 가용화과정은 상평형에 의하여 관찰하였다. 그 결과 게면활성제/물 2성분계와 3wt.%계면활성제/물/cyclohexane 3성분계는 각각 온도에 의존하는 것으로 나타났다. 계면활성제/물/cyclohexane계에서 3상영역은 $27^{\circ}C{\sim}32^{\circ}C$, $36^{\circ}C{\sim}45^{\circ}C$$38^{\circ}C{\sim}52^{\circ}C$의 온도 범위에서 각각 나타났으며 3상영역의 부근에서 물 및 오일의 가용화가 최대가 되었다. 계면활성제/물계의 온도변화에 따른 상거동을 살펴 본 결과 1-O-oleoyl glycerol은 hexagonal 액정상이, 2-O-oleoyl-myo-inositol 및 methyl 2-O-oleoyl-${\alpha}$-glucopyranoside는 lamella형태의 액정상이 관찰되었다.

  • PDF

마늘 정유물의 향기성분 및 저장 안정성 (Flavor Compounds and Storage Stability of Essential Oil from Garlic Distillation)

  • 조길석;김현구;하재호;박무현;신효선
    • 한국식품과학회지
    • /
    • 제22권7호
    • /
    • pp.840-845
    • /
    • 1990
  • 마늘에서 정유물을 증류하고 그 정유물의 휘발성 성분분석 및 저장안정성 시험을 실시하였다. 정유물을 포집하는데 사용한 pentane과 dichloromethane의 비는 2 : 1이었고, 정유물의 수율은 0.8 mm의 크기로 마쇄처리한 시료의 경우가 0.35%였고, 통마늘의 경우는 0.07%였다. 마늘 정유물에서 dimethyl sulfide, diallyl sulfide, methyl-1-propenyl disulfide, diallyl disulfide, allyl methyl sulfide, diallyl trisulfide 등의 6종류의 휘발성 물질이 동정되었고, diallyl trisulfide, diallyl disulfide, allyl methyl sulfide가 주요한 휘발성 성분이었다. 마늘 정유물을 $5^{\circ}C$$25^{\circ}C$에서 60일 동안 저장 중 품질 변화는 거의 일어나지 않았다.

  • PDF

Selective Ring-opening Fluorination of Epoxide: An Efficient Synthesis of 2'-C-Fluoro-2'-C-methyl Carbocyclic Nucleosides

  • Liu, Lian-Jin;Kim, Si-Wouk;Lee, Won-Jae;Hong, Joon-Hee
    • Bulletin of the Korean Chemical Society
    • /
    • 제30권12호
    • /
    • pp.2989-2992
    • /
    • 2009
  • An efficient synthetic route of novel 2′(${\alpha}$)-C-fluoro-2′(${\beta}$)-C-methyl carbocyclic nucleoside analogues is described. The key fluorinated intermediate 7 was prepared from the epoxide intermediate 5 via selective ring-opening of epoxide. Coupling of 7 with nucleosidic bases under the Mitsunobu reactions followed by deprotection afforded the target carbocyclic nucleoside analogues. The synthesized compounds were evaluated as inhibitors of the hepatitis C virus (HCV) in Huh-7 cell line in vitro.

A Study of Antibacterial Activity of Some Novel 8-Methoxy-4-methyl-quinoline Derivatives

  • Singh, Sheoraj;Kumar, Vikas;Kumar, Ashok;Sharma, Shalabh;Dua, Piyush
    • Bulletin of the Korean Chemical Society
    • /
    • 제31권12호
    • /
    • pp.3605-3610
    • /
    • 2010
  • In the present study, some quinoline derivatives have been synthesized like 8-methoxy-4-methyl-2-amino-(3'-chloro-2'-oxo-4'-substituted aryl-1'-azetidinyl)quinolines 8-12 and 8-methoxy-4-methyl-2-amino-(2'-substituted aryl-4'-oxo-1',3'-thiazolidin-3'-yl) quinolines 13-17 from 8-methoxy-4-methyl-2-(substituted arylidenyliminoamino)-quinolines 3-7. The structural assignments of these compounds were based on spectral (IR, $^1H$-NMR, Mass) and elemental (C, H, N) analysis. Further, these compounds were evaluated for antibacterial activity against various bacterial strains. Three compounds 10, 11 and 16 were found to exhibit potent antibacterial activity as compared to the standard drug amphicillin.

Synthesis of N-Alkylated 4-Fluoro-5-phenylpyrrole-2-carboxylate via Isolable Pyrroline Ionic Intermediates

  • Kim, Sung-Kwan;Jun, Chang-Soo;Kwak, Kyung-Chell;Park, Kwang-Yong;Chai, Kyu-Yun
    • Bulletin of the Korean Chemical Society
    • /
    • 제28권12호
    • /
    • pp.2324-2328
    • /
    • 2007
  • Organic fluorine chemistry produces many useful products. This paper elucidates the reaction of ethyl-4,4- difluoro-2-iodo-5-oxo-5-phenylpentanoate (2) with primary amines in a one-pot scheme. The reaction produced a series of β-fluoropyrrole derivatives at ambient temperatures. In this reaction, the less bulky the primary amine the higher was the resultant yield. When (2) and aqueous methylamine (40%) were allowed to react below 0 oC, 5-(ethoxycarboxyl)-1-methyl-3,3-difluoro-2-hydroxy-2-phenylpyrrolidine, an intermediate molecule for 2-ethyl-4-flouro-1-methyl-5-phenylpyrrole-2-carboxylate (5), was isolated first. Then, (5) reacted with hydroperchloric acid and acetic anhydride to form 5-(ethoxycarboxyl)-1-methyl-3,3-difluoro-2- phenylpyrrolinium perchlorate (6), which was converted to 2-ethyl-4-flouro-1-methyl-5-phenylpyrrole-2- carboxylate gradually in the presence of a base. Our experiments demonstrate that the formation of 2-ethyl-4- flouro-1-methyl-5-phenylpyrrole-2-carboxylate occurs via both one-pot schemes and stepwise pathways, depending on the reaction conditions. The isolation and characterization of the isolated intermediate (6) suggest an anionic pathway for this reaction.