• 제목/요약/키워드: Esters

검색결과 1,091건 처리시간 0.022초

Chiral Separation of Non-Steroidal Inflarnrnatory Drugs and Metabolites by Achiral Gas Chromatography as O- Trifluoroacetylated (- )-Menthyl Esters

  • Lee, Yoon-Suk;Paik, Man-Jeong;Kim, Kyoung-Rae
    • 대한약학회:학술대회논문집
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    • 대한약학회 2002년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2
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    • pp.396.3-397
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    • 2002
  • Because of the differences in biological and pharmacological properties between enantiomers of chiral acidic non-steroidal antiinflammatory drugs (NSAIDs) in human body. accurate determinations of their optical purities have been in great need. Racemic ibuprofen. tiaprofen. suprofen. flubiprofen and napoxen were reacted with (1R. 28. 5R)-(-)-menthol to convert them to corresponding diastereomeric (1R. 2S. 5R)-(- )-menthyl esters. (omitted)

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Phytochemistry and Bioassay Studies of Fijian Palaquium stehlinii Christoph (Sapotaceae)

  • Sotheeswaran, Subramanium;Sharif, Mirja;Ali, Sadaquat;Davies, Noel W.
    • Natural Product Sciences
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    • 제3권1호
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    • pp.55-58
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    • 1997
  • Water extract of the bark of Palaquium stehlinii has been bioassayed for antimicrobial activity and was found to inhibit the growth of Escherichia coli and Penicillium chrysogens. Phytochemical study revealed the presence of amyrin esters and 3,4',5,7-tetrahydroxyflavanone in the extract.

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High Temperature Lubrication with Phosphate Esters

  • Hanyaloglu, Bengi
    • Tribology and Lubricants
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    • 제11권5호
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    • pp.177-183
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    • 1995
  • Recent work with phosphate esters has shown that a lubricious polymeric film can formed from the vapor phase on interacting during and sliding. This lubrication technique has led to methods to reduce friction and wear to very low values at high temperatures up to 700$^{\circ}$C. Preliminary with synthetic tri aryl phosphates are very promising. The vaporized lubricant forms a polymeric film on the sliding and rolling surfaces reducing the coefficient of friction below 0.05. In-situ formation of the polymeric films shows that the polymer that is formed on the surface exists in different states depending on surface temperature.

Studies on the Lipid Classes of Nicotiana tabacum L. Seed Oil

  • Waheed, Amran;Mahmud, Shahid;Javed, Muhammad Akhtar;Saleem, Muhammad
    • Natural Product Sciences
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    • 제7권4호
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    • pp.110-113
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    • 2001
  • The lipid classes constituents; hydrocarbons, wax esters, sterol esters, triacylglycerols, free fatty acids, 1,3-diacylglycerols, 1,2-diacylglycerols, free sterols, 2-monoacylglycerols, 1-monoacylglycerols, phosphatidylethanolamines, phosphatidylcholines, lysophosphatidylethanolamines and phosphatidylinositols of Nicotiana tabacum L. seeds oil were investigated by thin layer and gas chromatography. Palmitic, oleic and linoleic acids were the major components in all lipid classes studied.

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Cinmetacin유도체의 합성과 진통항염활성 (Synthesis and Analgesic-antiinflammatory Activity of Cinmetacin Derivatives)

  • 임채욱;이종민;유재학;이현수;임철부
    • 약학회지
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    • 제45권1호
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    • pp.1-6
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    • 2001
  • Nine cinmetacin derivatives as potential nonsteroidal analgesic and antiinflammatory compounds were prepared and their analgesic-antiinflammatory activity was compared with cinmetacin. Salicylic acid and phenols were reacted with dicyclohexyl carbodiimide (DCC) to give phenol salicylates (1-4). Cinmetacin was treated with DCC and phenol derivatives to yield cinmetacin esters (5-13). Compounds (5, 7, 8, 10, 12, and 13) showed stronger analgesic activity than cinmetacin, but only compound (5) showed comparable antiinflammatory activity to cinmetacin.

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Malonyl Amino Acids and Their Esters as Psychoactive Agents I

  • Jain, Dilip;Tripathi, Meena;Kohli, D.V.;Uppadhyay, R.K.
    • Archives of Pharmacal Research
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    • 제15권2호
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    • pp.184-186
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    • 1992
  • Malonic acid amides were synthesized using different amino acids and their esters. THe synthesized compounds were evaluated for their sedative activity on rats. Potentiating effect of all the compounds on pentobarbitone induced sleep on rats was observed. Plasma protein binding studies were also carried out and it was observed that the synthesized compounds have low plasma protein binding as compared to barbiturates.

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Substituted Phenyl 2-Thiophenecarboxylates and Benzoates:Synthesis, NMR Spectra, and Aromaticity Index

  • 이창규;유지숙;박종석
    • Bulletin of the Korean Chemical Society
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    • 제21권1호
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    • pp.49-55
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    • 2000
  • A series of m-, and p-substituted phenyl 2-thiophenecarboxylates and benzoates was prepared by the reaction of the corresponding acyl chlorides and phenols. Their $^1H$ and $^{13}C$ NMR chemical shifts were analyzed using single substituent parameter (S SP) and dual substituent parameter (DSP) methods. The relative aromaticity index of thiophene was estimated to be 0.92 from the plot of the chemical shift of the carbonyl carbons of the thienoyl esters against chemical shift of the carbonyl carbons of the benzoyl esters.