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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Cytotoxic and anticonvulsant aryloxyaryl Mannich bases and related compounds.
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Cytotoxic and anticonvulsant aryloxyaryl Mannich bases and related compounds.

机译:细胞毒性和抗惊厥性芳氧基芳基曼尼希碱及相关化合物。

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摘要

A series of 1-(4-aryloxyphenyl)-3-diethylamino-1-propanone hydrochlorides 3a-3e and related compounds 3f, 3g and 4a-4d were synthesised. In addition, a group of 4-(4-aryloxyphenyl)-3-(4-aryloxyphenylcarbonyl)-1-ethyl-4-piperidinol hydrochlorides 6a-6e were prepared which incorporated most of the structural features of 3a-3e. All of these compounds displayed cytotoxic properties towards murine L1210 cells as well as human Molt 4/C8 and CEM T-lymphocytes. A number of these compounds possessed noteworthy potencies towards seven human colon cancer cell lines. Some correlations were noted between the IC(50) values generated in the different screens and the sigma, pi and molar refractivity constants of the aryl substituents as well as with the volumes and solvent accessible surface areas of various basic groups. Molecular modelling of representative compounds revealed structural features, which may have contributed to the varying potencies noted. In general, the compounds in series 6 were well tolerated whenadministered to mice. Anticonvulsant properties were demonstrated by a number of compounds in the maximal electroshock (MES) screen when administered intraperitoneally to mice while 4c and 6e afforded protection in the MES test when given orally to rats.
机译:合成了一系列1-(4-芳氧基苯基)-3-二乙基氨基-1-丙酮盐酸盐3a-3e和相关化合物3f,3g和4a-4d。此外,制备了一组4-(4-芳氧基苯基)-3-(4-芳氧基苯基羰基)-1-乙基-4-哌啶醇盐酸盐6a-6e,其结合了3a-3e的大部分结构特征。所有这些化合物均对鼠L1210细胞以及人类Molt 4 / C8和CEM T淋巴细胞表现出细胞毒性。这些化合物中的许多具有对七种人类结肠癌细胞系的显着效力。在不同屏幕中生成的IC(50)值与芳基取代基的sigma,pi和摩尔折射率常数之间以及与各种碱性基团的体积和溶剂可及表面积之间,发现了一些相关性。代表性化合物的分子模型揭示了结构特征,这可能导致了所述效力的变化。通常,当给小鼠施用时,系列6的化合物被很好地耐受。腹膜内给予小鼠最大电击(MES)筛选中的多种化合物证明了抗惊厥特性,而口服给予大鼠时4c和6e在MES试验中提供了保护作用。

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