• 제목/요약/키워드: alkyl compounds

검색결과 246건 처리시간 0.029초

6-(1-Alkenoyloxyalkyl)-5,8-dimethoxy-1,4-naphthoquinone Derivatives:Synthesis and Evaluation of Antitumor Activity

  • You, Young-Jae;Ahn, Byung-Zun
    • Archives of Pharmacal Research
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    • 제21권6호
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    • pp.738-743
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    • 1998
  • Thirty six 5,8-dimethoxy-1,4-naphthoquinone derivatives, which bear unsaturated alkyl side chain with ester bond, were synthesized and tested cytotoxic activity on L1210 cells a nd antitumor activity against ICR mice bearing S-180 cells. It could be recognized that the cytotoxicities of naphthoquinones with R1, being methyl and propyl (IV1~24) were not enhanced by replacing the alkanoyls with alkenoyls. In contrast, the introduction of the alkenoyl moieties on the compounds with $R_1$=hexyl (IV25~36) resulted in the enhancement of their cytotoxicities. Replacement of alkanoyl group with an alkenoyl group generally increased the T/C value of the mice bearing S-180 cells.

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김흠조 분묘 출토직물의 보존처리를 위한 물리.화학.생물학적 분석 (Analysis of Buried-Fabrics from the Tomb of Kim HeumJo by Physical Chemical and Biological Methods)

  • 이미식;박명자;배순화;이연희
    • 한국의류학회지
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    • 제23권6호
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    • pp.809-819
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    • 1999
  • The scientific analysis of buried fabrics from the 16th century tomb of Kim HeumJo was conducted focusing on the conservation of fabrics, In order to find out the appropriate cleaning solvent and detergent for historical textiles physical chemical and biological analysis was conducted. The following results are obtained from this study : 1, The buried fabrics from the tomb of Kim HeumJo were composed of cotton silk and ramie. Most of fabrics had lost their original colors faded to brown. It was revealed variations in weaves and patterns were very developed at that times. 2. The chemical components of soils are hydrocarbons alkyl alcohols nitrogen compounds aromatic organic acid which is supposed to be from a human body microorganisms and their by-products. 3. Seven kinds of fungi Actinomycetes Corynebacterium spp Micrococcus luteus Bacillus Clostridium were isolated from the fabrics. The most common fungus was Bacillus.

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순수 폴리프로필렌 섬유에 대한 소수성 염료의 흡착성과 염료의 molecular descriptor와의 상관성 분석 (Relationship Between the Affinity of Hydrophobic Dyes onto Pure Polypropylene and Molecular Descriptors of the Dyes)

  • 정종석;장경진;손송이;김태경;윤석한;김미경;홍진표
    • 한국염색가공학회:학술대회논문집
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    • 한국염색가공학회 2008년도 제38차 학술발표대회
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    • pp.120-122
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    • 2008
  • Relationship between hydrophobicity of dyes and affinity onto pure polypropylene fibers has been analyzed by using the molecular descriptor as a method to predict chemical and physical characteristics of compounds. Hydrophobicity of newly synthesized red dyes calculated by LogP which is one of molecular descriptors was increased continuously as the length of alkyl substituents increased. The dyeability onto polypropylene fibers was increased as LogP of the dyes increased and was very high when the hydrophobicity is over 6.

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Effect of n-Alkylamine Hydrochlorides on the Cloud Point of Nonionic Polyoxyethylated Surfactant

  • Han, Suk-Kyu;Kim, Young-Mi
    • 약학회지
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    • 제20권3호
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    • pp.156-161
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    • 1976
  • The salting in and salting out of Octoxynol, N.F., a nonionic polyoxyethylated surfactant by n-alkylamine hydrochlorides ws investigated by measuring their effect on the cloud point of the surfactant at various salt concentrations. The carbon number of the alkyl chain was varied from zero to twelve. Ammonium chloride, methylamine hydrochloride and ethylamine hydrochloride tended to salt out the surfactant, lowering its cloud point in proportion to the salt concentration. n-Ankylamine and n-butylamine hydrochlorides showed salting-out effect at low concentrations of the electrolyte, while their effects were leveled off and showed rather salting-in trend at higher concentrations of the electrolyte. These salting-in effect was ascribed to the formation of a hydrotropy of the n-alky lammonium cations with the surfactant. The higher homolog compounds of n-alkylamine hydrochlorides showed extraordinarily high salting-in effect at very low oncentrations of the electrolyte. These large salting-in effects were more drastic as the chain length was getting longer. These large increases of the cloud point of the surfactant were attributed to the formation of mixed micelles of n-alkylammonium cations with the polyoxyethylated surfactant.

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New Dielectric Polymers for Electronic Applications

  • Kravtsova, V;Soh, Deawha
    • 한국항해항만학회:학술대회논문집
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    • 한국항해항만학회 2000년도 추계학술대회논문집
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    • pp.101-103
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    • 2000
  • Research for the synthesis of high-temperature polymers by the photochemical method has been carrying out. The use of cheap and available compounds (viz. benzene, its alkyl, aryl and halogen substitutes, furan and maleic anhydride) subject to ultra violet irradiation resulted in a single stage quantitative yield of about 40 new polymers: polyimide films, enamel insulation, molding materials. At present experimental & industrial lots of wire have been produced. Polymer insulation possesses temperature exploitation range (from -l00$^{\circ}C$ to +300$^{\circ}C$ ) without significant changing of properties. As a result, new polyimide lacquers for production of a wide number of technical articles, such as polyimide films, fibres, enamel-wires, press-materials have been synthesized. An application field of the polyimides in membrane technology, printing plate and optic electronics manufactures has been outlined.

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Building Triketide α-Pyrone-Producing Yeast Platform Using Heterologous Expression of Sporopollenin Biosynthetic Genes

  • Kim, Sung Soo
    • Journal of Microbiology and Biotechnology
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    • 제25권11호
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    • pp.1796-1800
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    • 2015
  • Sporopollenin is a poorly characterized mixed aliphatic and aromatic polymer with ester and ether linkages. Recent studies have reported that α-pyrone polyketide compounds generated by Arabidopsis thaliana, polyketide synthase A (PKSA) and tetraketide α-pyrone reductase 1 (TKPR1), are previously unknown sporopollenin precursors. Here, the yeast Saccharomyces cerevisiae was introduced to test potential sporopollenin biosynthetic pathways in vivo. A PKSA/TKPR1 dual expressor was generated and various chain-length alkyl α-pyrones were identified by GC-MS. The growth rate of the strain containing PKSA/TKPR1 appeared normal. These results indicate that PKSA/TKPR1-expressing yeast would be a starting platform to investigate in vivo sporopollenin metabolism.

Anhydrous Proton Conducting Polymer Electrolytes Based on Poly(phosphonic acid)s and Oligomeric Triazole Compounds

  • Song, Myeong-Soo;Lee, Sung-Il;Bingoel Bahar;Meyer Wolfgang H.;Yoon, Do-Y.
    • 한국고분자학회:학술대회논문집
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    • 한국고분자학회 2006년도 IUPAC International Symposium on Advanced Polymers for Emerging Technologies
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    • pp.272-272
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    • 2006
  • In recent years, water-free polymer electrolyte membranes are attracting serious attention due to the possibility of the fuel cell operation at intermediate temperatures ($100{\sim}200^{\circ}C$). It was reported that phosphonic acids have proton conductivity under anhydrous conditions and in particular, relatively high proton conductivity could be obtained from the composite materials with heterocycles such as imidazole, pyrazole, etc. In this work, styrene based polymers, poly((4-vinylbenzyloxy)alkylphosphonic acid), which have phophonic acid group at the end of alkyl chain was synthesized. These polymers were analyzed in terms of thermal stability and proton conductivity. Additionally, cyclic oligosiloxanes tethered with triazole were prepared and analyzed.

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Nickel-Catalyzed Coupling of Arenesulfonates with Primary Alkylmagnesium Halides

  • Cho, Chul-Hee;Sun, Myung-Chul;Park, Kwang-Yong
    • Bulletin of the Korean Chemical Society
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    • 제26권9호
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    • pp.1410-1414
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    • 2005
  • Neopentyl arenesulfonates reacted with primary alkylmagnesium halides in the presence of $(PPh_3)_2NiCl_2$ to produce the corresponding alkylarenes. The efficiency of this coupling reaction considerably depends on the nature of catalyst and solvent. Highest yield was obtained by using three equivalents of Grignard reagent to a mixture of $(PPh_3)_2NiCl_2$ and arenesulfonate in refluxing $Et_2O$. This reaction represents a novel method allowing the efficient and creative substitution of sulfur-containing groups in aromatic compounds. It also shows that the alkyloxysulfonyl group might be a suitable alternative to halides and triflate in some circumstances.

Synthesis of certain 2-aminoadmantane derivatives as potential antimicrobial agents

  • Eisa, Hassan M.;Tantawy, Atif S.;El-Kerdawy, Mohamed-M.
    • Archives of Pharmacal Research
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    • 제13권1호
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    • pp.74-77
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    • 1990
  • N-(2-Amamantyl)-N-(5-arylhydrazono-6-methyl-4-oxopyrimidin-2-yl) guanidines (IIIa, b), 2-(2-admantyl-amino)-4-amino-s-triazine (IVa) and its 6-chloromethyl derivative (IVb) were prepared by cylization of 1-(2-admantyl) biguanide HCl (I) with ethyl 2-arylhydrazono-3-oxobutyrates (II), ethyl formate and ethyl chloroacetate, respectively. Where 1-(2-admantyl)-3-(4, 5-dioxo-2-imidazolidinylidene)guanidine (V) was used as intermediate for the synthesis of amides (VIIa, b), hydrazide (VIII) and azomethine derivatives (IX, b) of alkyl 2-(2-admantyl-amino)-4-amino-2-triazine-6-carboxylates (VI a, b). The antimicrobial testing of the prepared compounds proved that compound 1Xb was the most active. It showed a marked bacteriostatic effect against Staphylococcus aureus and Bacillus subtilis.

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New Synthesis of 2-Substituted Imidazo[2, 1-b]thiazoles and their Antimicrobial Activities

  • Mahfouz, A.Abdel Aziz;Elhabashy, F.M.
    • Archives of Pharmacal Research
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    • 제13권1호
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    • pp.9-13
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    • 1990
  • 4, 5-Diphenyl-2-mercaptiomidazole (I) was reacted with hydraziodyl halides IIa-d togive the S-alkyl derivatives III-a-d. Cyclization of IIIa-d afforded imidazo[2, 1-b]-thiazole derivatives Vla, b and VII. Treatment of 1 with a-chloroethylacetoaccetate (IV) gave ethyl 2(4, 5-diphenyl-2-imidazolinylthio)-3-keto-butyrate (V). Compound V coupled with benzendiazonium chloride to give the corresponding phenylhydrazo compound IIId. On heating V with polyphosphoric acid, cyclization took place and 2-acetyl-5, 6-diphenyl-imidazo [2, 1-b] thiazol-3-one (VIII) was obtained. The compound VIII was condensed with aromatic aldehydes to yield the cinnamoyl derivatives 1Xa, b. The antimicrobial activities of compounds IIIa-d, V, VIa, VII were examined.

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