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N6-substituted adenosines. Cytokinin and antitumor activities

Svetlana V. Kolyachkina, Vitali I. Tararov, Cyril S. Alexeev, Dmitry M. Krivosheev, Georgy A. Romanov, Evgenia V. Stepanova, Eliso S. Solomko, Andrey N. Inshakov and Sergey N. Mikhailov

. 2011 ; 76 (11) : 1361-1378.

Jazyk angličtina Země Česko Médium elektronický zdroj

Perzistentní odkaz   https://www.medvik.cz/link/bmc12022665
E-zdroje Online

NLK ProQuest Central od 2005-01-01 do 2011

A series of N6-adenosine derivatives were synthesized by alkylation of N6-acetyl-2′,3′,5′-tri-O-acetyladenosine (1) with alkyl halides and alcohols. It was shown that propargyl derivative 2a is a good substrate for copper(I) catalyzed Huisgen [3+2] cycloaddition with azides. This click-reaction can be used for preparation of the libraries of 1,2,3-triazolyl modified adenosines. Biological activities of N6-adenosines were studied in two plant and six human cancer cell assays. The remarkable parallel between cytokinin and cytotoxic activities was found. The most cytokinin active compounds 3c–3e at the same time appeared to be the most potent cytotoxic agents.

N6-substituted adenosines. Cytokinin and antitumor activities [elektronický zdroj] /

Bibliografie atd.

Literatura

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