4.7 Article

Piperazine N-substituted naphthyridines, pyridothienopyrimidines and pyridothienotriazines:: new antiprotozoals active against Philasterides dicentrarchi

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EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
卷 38, 期 3, 页码 265-275

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ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/S0223-5234(03)00032-1

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1,8-naphthyridine; pyridothienopyrimidine; pyridothienotriazine; antiprotozoal

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New antiprotozoals active against Philasterides dicentrarchi, the causative agent of scuticociliatosis in farmed turbot and Black Sea bass-bream, have been synthesised and tested. The most active compounds posses a piperazine ring, generally N-bonded to the heterocycle, and are the 1,8-naphthyridines, 2f and 5o, the pyridothienopyrimidine (7), and the pyridothienotriazines, 8, 9, 12d, 12f, 12h, 12m and 12k. Pyridothienotriazine (12k) presents the same activity (Lethal Dose, LD = 0.8/1.5 mg L-1) as the well-known antiparasitics niclosamide and oxyclozanide. (C) 2003 Editions scientifiques et medicales Elsevier SAS. All rights reserved.

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