2,3-dihydro-1h-cyclopenta[b]quinoline derivatives as acetylcholinesterase inhibitors—synthesis, radiolabeling and biodistribution2,3-dihydro-1h-cyclopenta[b]喹啉衍生物作为乙酰胆碱酯酶inhibitors-synthesis,放射性标记和biodistribution.pdfVIP

2,3-dihydro-1h-cyclopenta[b]quinoline derivatives as acetylcholinesterase inhibitors—synthesis, radiolabeling and biodistribution2,3-dihydro-1h-cyclopenta[b]喹啉衍生物作为乙酰胆碱酯酶inhibitors-synthesis,放射性标记和biodistribution.pdf

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2,3-dihydro-1h-cyclopenta[b]quinoline derivatives as acetylcholinesterase inhibitors—synthesis, radiolabeling and biodistribution2,3-dihydro-1h-cyclopenta[b]喹啉衍生物作为乙酰胆碱酯酶inhibitors-synthesis,放射性标记和biodistribution

Int. J. Mol. Sci. 2012, 13, 10067-10090; doi:10.3390/ijms130810067 OPEN ACCESS International Journal of Molecular Sciences ISSN 1422-0067 /journal/ijms Article 2,3-Dihydro-1H-cyclopenta[b]quinoline Derivatives as Acetylcholinesterase Inhibitors—Synthesis, Radiolabeling and Biodistribution Paweł Szymański 1,*, Alice Lázničková 2, Milan Lázniček 2, Marek Bajda 3, Barbara Malawska 3, 1 1 Magdalena Markowicz and Elżbieta Mikiciuk-Olasik 1 Department of Pharmaceutical Chemistry and Drug Analyses, Medical University, ul. Muszyńskiego 1, Lodz 90-151, Poland; E-Mails: magdalena.markowicz@umed.lodz.pl (M.M.); elzbieta.mikiciuk-olasik@umed.lodz.pl (E.M.-O.) 2 Faculty of Pharmacy in Hradec Kralove, Charles University in Prague, Heyrovskeho 1203, Hradec Kralove CZ-50005, Czech Republic; E-Mails: alice.laznickova@faf.cuni.cz (A.L.); milan.laznicek@faf.cuni.cz (M.L.) 3 Department of Physicochemical Drug Analysis, Faculty of Pharmacy, Jagiellonian University Medical College, Medyczna 9, Krakow 30-688, Poland; E-Mails: marek.bajda@.pl (M.B.); barbara.malawska@.pl (B.M.) * Author to whom correspondence should be addressed; E-Mail: pawel.szymanski@umed.lodz.pl; Tel./Fax: +48-42-677-9250. Received: 14 June 2012; in revised form: 7 July 2012 / Accepted: 6 August 2012 / Published: 13 August 2012 Abstract: In the present study we describe the synthesis and biological assessment of new tacrine analogs in the course of inhibitio

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