Advertisement

Pharmaceutical Chemistry Journal

, Volume 23, Issue 12, pp 990–995 | Cite as

Synthesis, anti-inflammatory activity and metabolism of alkyl aryl ketones and their derivatives

  • V. K. Daukshas
  • P. G. Gaidyalis
  • É. B. Udrenaite
  • L. K. Labanauskas
  • G. A. Gasperavichene
  • L. F. Gumbaragite
  • D. V. Ramanauskas
Search for New Drugs
  • 92 Downloads

Keywords

Organic Chemistry Ketone Alkyl Aryl Aryl Ketone Alkyl Aryl Ketone 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

Literature cited

  1. 1.
    M. L. Belen'kii, Elements of Quantitative Evaluation of Pharmacological Effect [in Russian], 2nd Edn., Leningrad (1963), pp. 81–106.Google Scholar
  2. 2.
    V. K. Daukshas, P. G. Gaidyalis, O. Yu. Pyatrauskas, et al., Khim.-farm. Zh., 569–573 (1987).Google Scholar
  3. 3.
    T. N. Dorofeenko and G. A. Korol'chenko, Izv. Vyssh. Uchebn. Zavedenii SSSR: Khim. Khim. Tekhnol.,5, 932–934 (1962).Google Scholar
  4. 4.
    A. V. El'tsov, Zh. Obshch. Khim.,34, 1303–1307 (1964).Google Scholar
  5. 5.
    W. H. Beech, J. Chem. Soc., 1297–1302 (1954).Google Scholar
  6. 6.
    G. Brucker, G. Fodor, J. Kiss, et al., J. Chem. Soc., 885–890 (1948).Google Scholar
  7. 7.
    V. K. Daukšas, G. V. Purvaneckas, E. B. Udrenaite, et al., Heterocycles,15, 1395–1404 (1981).Google Scholar
  8. 8.
    C. Feugeas, Bull. Soc. Chim., Fr., No. 8, 1892–1895 (1964).Google Scholar
  9. 9.
    Ch. Granito and H. P. Schultz, J. Org. Chem.,28, 879–881 (1963).Google Scholar
  10. 10.
    U. Hamao and T. Tomio, Japanese Patent No. 52 139789 (1976); Ref. Zh. Khim., No. 12, No. 120318 P (1979).Google Scholar
  11. 11.
    H. G. Hege, H. Lietz, and J. Weymann, Arzneim.-Forsch.,34, 972–979 (1984).Google Scholar
  12. 12.
    R. Huisingen, G. Seidl, and J. Wimmer, Liebigs Ann. Chem.,677, 21–23 (1964).Google Scholar
  13. 13.
    J. Iwao and M. Samejima, J. Pharm. Soc. Jpn.,74, 548–550 (1954); Chem. Abstr.,49, 8174d (1955).Google Scholar
  14. 14.
    T. Kametani, K. Ogasawara, A. Kozuka, et al., Jakugaku Zashi,87, 1189–1194 (1967); Chem. Abstr.,68, 95651d (1968).Google Scholar
  15. 15.
    J. Marek, Pharmazie,36, 46–49 (1981).Google Scholar
  16. 16.
    R. H. Moffet, A. R. Hanze, and R. H. Seay, J. Med. Chem.,7, 178–186 (1964).Google Scholar
  17. 17.
    F. Parrini and R. G. E. Morales, Spectroscopy,4, 307–316 (1974).Google Scholar
  18. 18.
    A. Robertson, W. F. Sandrock, and C. B. Hendry, J. Chem. Soc., 2426–2432 (1931).Google Scholar
  19. 19.
    J. Sauer and H. Niebert, Chem. Ber.,97, 3208–3218 (1964).Google Scholar
  20. 20.
    A. B. Swanson, D. D. Chambliss, J. C. Blomquist, et al., Mutat. Res.,60, 143–153 (1979); Ref. Zh. Biokhim., No. 16 - No. 16x 98 (1979).Google Scholar
  21. 21.
    S. Tanura, H. Okubo, and H. Kaneta, Nippon Nogei-Kagaku Kaishi,28, 4–8 (1954); Chem. Abstr.,51 (1957).Google Scholar
  22. 22.
    C. A. Winter, E. A. Richley, and G. W. Nuss, Proc. Soc. Exp. Biol. (N.Y.),111, 544–547 (1962).Google Scholar

Copyright information

© Plenum Publishing Corporation 1990

Authors and Affiliations

  • V. K. Daukshas
    • 1
  • P. G. Gaidyalis
    • 1
  • É. B. Udrenaite
    • 1
  • L. K. Labanauskas
    • 1
  • G. A. Gasperavichene
    • 1
  • L. F. Gumbaragite
    • 1
  • D. V. Ramanauskas
    • 1
  1. 1.V. Kapsukas Vil'nyus UniversityUSSR

Personalised recommendations