Synthesis and caspase-3 inhibitory activity of 8-sulfonyl-1,3-dioxo-2,3-dihydro-1H-pyrrolo[3,4-c]quinolines

Dmitri V. Kravchenko , Volodymyr M. Kysil , Sergey E. Tkachenko , Sergey Maliarchouk , Ilya M. Okun , Alexandre V. Ivachtchenko
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引用次数: 24

Abstract

A convenient synthesis of novel 8-sulfonyl-1,3-dioxo-4-methyl-2,3-dihydro-1H-pyrrolo[3,4-c]quinolines is described. As key steps to assemble the target molecular scaffold, our method features (a) Pfitzinger reaction of isatin-5-sulfonate 1 with methyl 3-oxo-3-phenylpropanoate, (b) formation of 1-(1H-pyrazol-4-yl)-1H-pyrrole-2,5-dione intermediate 5, and (c) reaction of sulfinic acid 9 with acrylate or methylacrylate leading to the corresponding sulfonyl propionates. Two compounds, ester 11 and morpholide 13, have been identified as potent inhibitors of caspase-3 with IC50 = 6 nM. Our primary data suggest noncompetitive and reversible character of caspase-3 inhibition.

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8-磺酰基-1,3-二氧基-2,3-二氢- 1h -吡咯啉[3,4-c]喹啉的合成及caspase-3抑制活性
介绍了一种新型8-磺酰基-1,3-二氧基-4-甲基-2,3-二氢- 1h -吡咯[3,4-c]喹啉化合物的简便合成方法。作为组装目标分子支架的关键步骤,我们的方法包括(a) isatin-5-磺酸1与甲基3-氧-3-苯基丙酸甲酯的Pfitzinger反应,(b) 1-(1h -吡唑-4-基)- 1h -吡咯-2,5-二酮中间体5的生成,以及(c)亚磺酸9与丙烯酸酯或甲基丙烯酸酯反应,生成相应的丙磺酸磺酰酯。两种化合物,酯11和morpholide 13,已被鉴定为有效的caspase-3抑制剂,IC50 = 6 nM。我们的主要数据表明caspase-3抑制具有非竞争性和可逆性。
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