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N-phosphorylated 3,5-bis(arylidene)4-piperidones: Synthesis, X-ray structure, and evaluation of antitumor activity

✍ Scribed by Irina L. Odinets; Oleg I. Artyushin; Evgenii I. Goryunov; Konstantin A. Lyssenko; Ekaterina Yu. Rybalkina; Ilya V. Kosilkin; Tatiana V. Timofeeva; Mikhail Yu. Antipin


Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
123 KB
Volume
16
Category
Article
ISSN
1042-7163

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✦ Synopsis


In a search for cytotoxic fluorescent ma- terials, a series of N-phosphorylated compounds 2a-c were prepared by phosphorylation of 3,5-bis(4-N,Ndimethylbenzylidene)-4-piperidone 1. According to X-ray investigations, molecule 2a is E,E-isomer with axial position of the P(O)(OCH 2 CF 3 ) 2 substituent. Fluorescence of compounds 2a-c was found to be similar to fluorescence of nonphosphorylated compound 1. The cytotoxicity of the compounds 2a-c was estimated on several human tumor cell lines (H9, K562, and MCF7).


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