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Synthesis and Evaluation of Antiparasitic Activities of New 4-[5-(4-Phenoxyphenyl)-2H-pyrazol-3-yl]morpholine Derivatives

机译:新型4- [5-(4-苯氧基苯基)-2H-吡唑-3-基]吗啉衍生物的合成及抗寄生虫活性的评价

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摘要

A series of new 4-[5-(4-phenoxyphenyl)-2H-pyrazol-3-yl]morpholine derivatives,prepared by two synthetic routes,were in vitro assayed against three Trypanosoma strains,Leishmania donovani,and Plasmodium falciparum K1.Seven out of 17 compounds showed moderate to very good activity against blood stage T.b.rhodesiense,with 10 and 17 exhibiting highest potency(IC50 of 1.0 and 1.1 mu M,respectively).Interestingly,the beta-diketone precursors 1-3 had good antitrypanosomal activity toward the insect stage,with IC50 values of 1.0-3.4 mu M.Among different compounds with moderate activity against T.cruzi,compound 17 showed the lowest IC50 value of 9.5 mu M;thus,the series seemed to act selectively toward the different Trypanosoma parasites.Eight compounds were moderately active against L.donovani,with 2,3,and 12 being the most promising ones(IC50 values of 2.3-5.2 mu M),whereas compound 14 was the only derivative with good activity against P.falciparum(IC50 of 3.7 mu M).
机译:用两种合成方法制备了一系列新的4- [5-(4-(苯氧基苯基)-2H-吡唑-3-基]吗啉衍生物,对三种锥虫,利什曼原虫和恶性疟原虫K1进行了体外测定。七在17种化合物中,对Tbhodesiense的血液阶段具有中等至非常好的活性,其中10和17种具有最高的效价(IC50分别为1.0和1.1μM)。有趣的是,β-二酮前体1-3具有良好的抗锥虫活性在昆虫阶段,IC50值为1.0-3.4μM。在对T.cruzi有中等活性的不同化合物中,化合物17的最低IC50值为9.5μM;因此,该系列似乎选择性地作用于锥虫的不同寄生虫八种化合物对唐氏疟原虫具有中等活性,其中2,3和12是最有前途的化合物(IC50值为2.3-5.2μM),而化合物14是唯一对恶性疟原虫具有良好活性的衍生物(IC50)。 3.7微米)。

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