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Discovery of colon tumor cell growth inhibitory agents through a combinatorial approach.

机译:通过组合方法发现结肠肿瘤细胞生长抑制剂。

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摘要

Two series with the general formula of 4,6-diaryl-2-oxo-1,2 dihydropyridine-3-carbonitriles and their isosteric 4,6-diaryl-2-imino-1,2-dihydropyridine-3-carbonitrile were synthesized through one pot reaction of the appropriate acetophenone, aldehyde, ammonium acetate with ethyl cyanoacetate or malononitrile, respectively. The synthesized compounds were evaluated for their tumor cell growth inhibitory activity against the human HT-29 colon tumor cell line, as well as their PDE3 inhibitory activity. Compound 4-(2-Ethoxyphenyl)-2-oxo-6-thiophen-3-yl-1,2-dihydropyridine-3 carbonitrile (21) showed tumor cell growth inhibitory activity with an IC50 value of 1.25 microM. Meanwhile, 4-(4-Ethoxyphenyl)-2-imino-6-(thiophen-3-yl)-1,2-dihydropyridine-3-carbonitrile (26) showed inhibitory effect upon PDE3 using cAMP or cGMP as substrate. No correlation exists between PDE3 inhibition and the tumor cell growth inhibitory activity. Docking compound 21 to other possible molecular targets showed the potential to bind PIM1 Kinase.
机译:用4,6-二芳基-2-氧代-1,2二氢吡啶-3-碳腈的通式两种系列及其取缔素4,6-二芳基-2-亚氨基-1,2-二氢吡啶-3-块腈适当乙酮,醛,乙酸铵与乙酸乙酯或丙二酸铵的一个罐式反应。评价合成的化合物对人HT-29结肠肿瘤细胞系的肿瘤细胞生长抑制活性,以及​​它们的PDE3抑制活性。化合物4-(2-乙氧基苯基)-2-氧代-6-噻吩-3-基-1,2-二氢吡啶-3碳腈(21)显示肿瘤细胞生长抑制活性,IC50值为1.25微米。同时,4-(4-乙氧基苯基)-2-亚氨基-6-(噻吩-3-基)-1,2-二氢吡啶-3-腈(26)在PDE3使用阵营或CGMP作为底物显示抑制作用。 PDE3抑制与肿瘤细胞生长抑制活性之间不存在相关性。将化合物21对接至其他可能的分子靶标显示有可能结合PIM1激酶的潜力。

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