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A-mini-review-on-Biginelli-adducts-with-notable-pharmacological-properties.pdf

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A-mini-review-on-Biginelli-adducts-with-notable-pharmacological-properties

Journal of Advanced Research (2015) 6, 363–373Cairo University Journal of Advanced ResearchMINI REVIEWA mini-review on Biginelli adducts with notable pharmacological properties* Corresponding author. Tel.: +55 31 3409 6373; fax: +55 31 3409 5700. E-mail address: adefatima@qui.ufmg.br (A?. de Fa?tima). Peer review under responsibility of Cairo University. Production and hosting by Elsevier /10.1016/j.jare.2014.10.006 2090-1232 a 2014 Production and hosting by Elsevier B.V. on behalf of Cairo University.A?ngelo de Fa?tima a,*, Taniris C. Braga a, Leonardo da S. Neto a, Bruna S. Terra a, Breno G.F. Oliveira a, Daniel L. da Silva a, Luzia V. Modolo ba Departamento de Qu??mica, Instituto de Cie?ncias Exatas, Universidade Federal de Minas Gerais, Av. Pres. Anto?nio Carlos, 6627, Pampulha, Belo Horizonte, MG 31270-901, Brazil b Departamento de Bota?nica, Instituto de Cie?ncias Biolo?gicas, Universidade Federal de Minas Gerais, Av. Pres. Anto?nio Carlos, 6627, Pampulha, Belo Horizonte, MG 31270-901, BrazilG R A P H I C A L A B S T R A C TA R T I C L E I N F O Article history: Received 18 August 2014 Received in revised form 5 October 2014A B S T R A C T Since the disclosure of Biginelli reaction by the chemist Pietro Biginelli, functionalized 3,4-dihy- dropyrimidin-2(1H)-ones/thiones (DHPMs) have emerged as prototypes for the design of compounds with a broad variety of biological activities. This mini-review describes over 100 Biginelli adducts demonstrated to be promising anticancer, inhibitors of calcium channel, 364 A?. de Fa?tima et al.Accepted 24 October 2014 Available online 1 November 2014 Keywords: Biginelli adducts Antiproliferative activity cancer Calcium channel Antimicrobial activity AntioxidantsA?ngelo de Fa?tima rece in Science in 200 University of Campin currently Associate Department of Chem University of Minas G Dr. de Fa?tima is the Network for the De Urease Inhibitors (w Group of Studies Biological Chemistry ests include the synthesis of molecules with b

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