aurones a promising heterocyclic scaffold for the development of potent antileishmanial agentsaurones有前途的杂环支架的发展强有力的antileishmanial代理.pdfVIP
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aurones a promising heterocyclic scaffold for the development of potent antileishmanial agentsaurones有前途的杂环支架的发展强有力的antileishmanial代理
Hindawi Publishing Corporation
International Journal of Medicinal Chemistry
Volume 2012, Article ID 196921, 8 pages
doi:10.1155/2012/196921
Research Article
Aurones: A Promising Heterocyclic Scaffold for the Development
of Potent Antileishmanial Agents
Marina Roussaki,1 Sofia Costa Lima,2 Anna-Maria Kypreou,1 Panagiotis Kefalas,3
Anabela Cordeiro da Silva,2, 4 and Anastasia Detsi1
1 Laboratory of Organic Chemistry, School of Chemical Engineering, National Technical University of Athens,
Heroon Polytechniou 9, Zografou Campus, 15780 Athens, Greece
2 Parasite Disease Group, IBMC-Institute for Molecular and Cell Biology, University of Porto, Rua do Campo Alegre,
823, 4150-180 Porto, Portugal
3 Department of Food Quality and Chemistry of Natural Products, Mediterranean Agronomic Institute of Chania,
International Centre for Advanced Mediterranean Agronomic Studies, 73100 Chania, Crete, Greece
4 Department of Biological Sciences, Faculty of Pharmacy, University of Porto, Rua de Jorge Viterbo Ferreiera,
228, 4050-313 Porto, Portugal
Correspondence should be addressed to Anastasia Detsi, adetsi@chemeng.ntua.gr
Received 27 May 2012; Accepted 31 July 2012
Academic Editor: O. Bruno
Copyright © 2012 Marina Roussaki et al. This is an open access article distributed under the Creative Commons Attribution
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly
cited.
A series of (Z )-2-benzylidenebenzofuran-3-(2H)-ones (aurones) bearing a variety of substituents on rings A and B were
synthesized and evaluated for their antiparasitic activity against the intracellular amastigote form of Leishmania infantum and their
cytotoxicity against human THP1-diff
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