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作为潜在抗丝虫和抗肿瘤药物的2,4-二取代噻唑和硒唑的合成。2. 2-氨基-4-(异硫氰酸甲酯基)噻唑和2-氨基-4-(异硫氰酸甲酯基)硒唑的2-芳基酰胺和2-烷基酰胺衍生物。

Synthesis of 2,4-disubstituted thiazoles and selenazoles as potential antifilarial and antitumor agents. 2. 2-Arylamido and 2-alkylamido derivatives of 2-amino-4-(isothiocyanatomethyl)thiazole and 2-amino-4-(isothiocyanatomethyl)selenazole.

作者信息

Kumar Y, Green R, Wise D S, Wotring L L, Townsend L B

机构信息

Department of Medicinal Chemistry, College of Pharmacy, University of Michigan, Ann Arbor 48109-1065.

出版信息

J Med Chem. 1993 Nov 26;36(24):3849-52. doi: 10.1021/jm00076a013.

Abstract

The synthesis of a series of 2-arylamido and 2-alkylamido derivatives of 2-amino-4-(isothiocyanatomethyl)thiazole and 2-amino-4-(isothiocyanatomethyl)selenazole is described. In vitro antiproliferative evaluations were carried out using L1210 cells. The 2-(alkylamido)thiazole derivatives were moderately antiproliferative, with IC50's of 4-8 microM. A significant increase in activity was obtained for the arylamido derivatives, with IC50's of 0.2-1 microM. The results obtained for the selenazoles were similar to those for the thiazoles. 2-Benzamido-4-(isothiocyanatomethyl)-thiazole (19) was found to be a potent inhibitor of GMP synthetase. None of the compounds prepared in this study demonstrated antifilarial activity.

摘要

本文描述了一系列2-氨基-4-(异硫氰酸甲酯基)噻唑和2-氨基-4-(异硫氰酸甲酯基)硒唑的2-芳基酰胺和2-烷基酰胺衍生物的合成。使用L1210细胞进行了体外抗增殖评估。2-(烷基酰胺基)噻唑衍生物具有中等程度的抗增殖活性,IC50为4-8微摩尔。芳基酰胺衍生物的活性显著增加,IC50为0.2-1微摩尔。硒唑的结果与噻唑相似。发现2-苯甲酰胺基-4-(异硫氰酸甲酯基)噻唑(19)是GMP合成酶的有效抑制剂。本研究中制备的化合物均未表现出抗丝虫活性。

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