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Synthesis, Pharmacological Properties and SAR of New 1,4-Disubstituted Pierazine Derivatives with Hypnotic-Sedative Activity

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Synthesis, chromatographic behaviour, pharmacological data and structure activity relationship (SAR) studies of some 1-(pyrimidin-2-yl)piperazine derivatives 1-13 are reported. The hydrophobic indices and chromatographic retention factors of the compounds exhibited statistically significant linear correlation with the calculated lipophilicities. The highest hypnotic-sedative activity as measured in loss of the righting reflex, rota-rod and spontaneous locomotor activity tests exhibited compound6 possessing n-hexyl R substituent. The hypnotic activity of compounds 1-13 measured in loss of the righting reflex test could be described with the aid of hydrophobic indices in terms of Hansch parabolic relationship for structurally related group of compounds (separately for compounds withR= alkyl orR= cycloalkyl). The necessity to describe the pharmacological activity for aliphatic and alicyclic series with 2 different equations corresponded well to the observed difference in the pharmacological properties between the both
Słowa kluczowe
Rocznik
Strony
1027--1037
Opis fizyczny
Bibliogr. 27 poz., rys.
Twórcy
  • Insitute of Chemistry, University of Białystok, 15-443 Białystok, Piłsudskiego 11/4, Poland
  • National Institute of Public Health, 00-725 Warszawa, Chełmska 30/34, Poland
autor
  • Pharmaceutical Research Institute, 01-793 Warszawa, Rydygiera 8, Poland
  • Institute of Pharmacology, Polish Academy of Sciences, 31-343 Krakow, Smêtna 12, Poland
  • Institute of Pharmacology, Polish Academy of Sciences, 31-343 Krakow, Smêtna 12, Poland
  • Institute of Pharmacology, Polish Academy of Sciences, 31-343 Krakow, Smętna 12, Poland
autor
  • Insitute of Chemistry, University of Białystok, 15-443 Białystok, Piłsudskiego 11/4, Poland
Bibliografia
  • 1. Milewski S., Mignini F., Prasad R. and Borowski E., Antimicr. Agents Chemother., 45, 223 (2001).
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  • 3. Dzieduszycka M., Martelli S., Arciemiuk M., Bontemps-Gracz M.M., Kupiec A. and Borowski E., Bioorg. Med. Chem., 10, 1025 (2002).
  • 4. Tarasiuk J., Stefańska B., Plodzich I., Tkaczyk-Gobis K., Seksek O., Martelli S., Gamier-Suillerot and Borowski E., Brit. J. Pharmacol., 135, 1513 (2002).
  • 5. Stefańska B., Arciemiuk M., Bontemps-Gracz M.M., Dzieduszycka M., Kupiec A., Martelli S. and Borowski E., Bioorg. Med. Chem., 11, 561 (2003).
  • 6. Kubinyi H., QS AR: Hansch Analysis and Related Approaches., Eds. R. Mannhold, P. Krosgaard-Larsen and H. Timmerman, VCH, Weinheim, New York, Basel, Cambridge, Tokyo, 1993, Ch 3.
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  • 12. Haefely W.E., Allosteric Modulation of Amino Acid Receptors. Therapeutic Implications., Eds. E.A. Barnard and E. Costa, Raven Press Ltd., New York 1989, p. 47.
  • 13. Harvey S.C., The Pharmacological Bases of Therapeutics 7th ed., Eds. A.G. Gilman, L.S. Goodman, T.W. Rail, F. Murad, Macmillan, NY 1985, Ch. 17.
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  • 18. Chilmonczyk Z., Mazgajska M., Bogdal M., Cybulski J. and Lewandowska U., Pol J. Pharmacol., 48, 431 (1996).
  • 19. Chilmonczyk Z., Mazgajska M., Iskra-Jopa J., Chojnacka-Wójcik E., Tatarczyńska E., Kłodzińska A. and Nowak J.Z., J. Pharm Pharmacol, 54, 689 (2002).
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Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BUJ1-0024-0052
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