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New Glycoside Derivatives of 6H-Indolo{2,3-b]quinolines

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
The series of carbohydrate derivatives of 6H-indolo[2,3-b]quinoline was obtained. Carbohydrate units (2-deoxy-D-glucose, 2-deoxy-D-lactose and 2-deoxy-L-rhamnose) were coupled viaa glycosidic bond to a hydroxyl group placed in a side chain at selected positions of indoloquinoline. Increased solubility was noted for all obtained products. Some of them exhibit also increased in vitro cytotoxicity.
Rocznik
Strony
369--386
Opis fizyczny
Bibliogr. poz. 17, rys.
Twórcy
  • Pharmaceutical Research Institute, ul. Rydygiera 8, 01-793 Warszawa, Poland
  • Pharmaceutical Research Institute, ul. Rydygiera 8, 01-793 Warszawa, Poland
autor
  • Pharmaceutical Research Institute, ul. Rydygiera 8, 01-793 Warszawa, Poland
autor
  • Institute of Immunology and Experimental Therapy, PAS, ul. Weigla 12, 53-114 Wrocław, Poland
autor
  • Institute of Immunology and Experimental Therapy, PAS, ul. Weigla 12, 53-114 Wrocław, Poland
  • Institute of Organic Chemistry, Biochemistry and Biotechnology, Wrocław University of Technology, Wybrzeże Wyspiañskiego 27, 50-370 Wrocław, Poland
Bibliografia
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  • 8. Rodrigues-Pereira E., Belin L., Sancelme M., Prudhomme M., Ollier M.., Rapp M., Servcre D., Riou .l.F. and Fabbro D., .J. Med. Chem., 39, 4471 (1996); Bailly C., Riou J. F., Colson P., Houssier C., Rodrigues-Pereira E. and Prudhomme M.,Biochemist1y, 36, 3917 (1997); ShankarB. B. and McCombic S.W., TetrahedronLett., 35, 3005 (1994); Chisholm J.D. and Van Vranken D.L.,J. Org. Chem., 65, 8406 (2000). [Erratum for Vol. 65, 2000].
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Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BUJ3-0002-0009
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