Synthesis and anticancer activity of 1-(41-isopropylphenyl)-4-(42-chlorophenyl)5,6,7,8-tetrahydro-2,4а-diazacyclopenta[cd]azulene-2-carboxylic acid arylamides against PC-3 prostate cancer cells

S. A. Demchenko, Yu. A. Fedchenkova, T. Bukhtiarova, L. Bobkova, V. Sukhoveev, А. М. Demchenko
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Abstract

Pharmacotherapy of prostate cancer is an important part in combating oncologic diseases. This is very relevant, because prostate cancer is a cause of 10 % of deaths from all cancerous diseases in males. The aim of the study – to synthesize novel derivatives of 1-(41-isopropylphenyl)-4-(42-chlorophenyl)5,6,7,8-tetrahydro-2,4а-diazacyclopenta[cd]azulene-2-carboxylic acid arylamides and to evaluate their antitumor activity against PC-3 prostate cancer cells. By reaction of equimolar amounts of 2-methoxy-3,4,5,6-tetrahydro-7H-azepine with a-amino-4-chloroacetophenone chlorohydrate, 3-(4-chlorophenyl)-6,7,8,9- tetrahydro-5Н-imidazo[1,2-a]azepine was synthesized. By alkylation of a-bromo-4-іsopropylacetophenone in ethylacetate and following treatment of the obtained intermediary quaternary salt with excess of 5 % NaOH solution,1-(41-isopropylphenyl)-4-(42chlorophenyl)-5,6,7,8-tetrahydro-2,4а-diazacyclopenta[cd] azulene was synthesized. By boiling it with equimolar amounts of correspondding arylisocyanates in dried benzol, an array of 1-(41-iso propylphenyl)-4(42-chlorophenyl)-5,6,7,8-tetrahydro-2,4а-diazacyclopenta[cd]azulene-2-carboxylic acid arylamides were synthesized. Structure and purity of all compounds obtained were confirmed by data of MR1Н spectroscopy. Lipophilicity (LogP) of compounds 6 and 8 a-i was calculated with the ACD LogP program. Antitumor activity of 1-(41-isopropylphenyl)-4-(42-chlorophenyl)-5,6,7,8-tetrahydro-2,4а-diazacyclopenta[cd]azulene-2-carboxylic acid (3-methylphenyl) and (3-methoxyphenyl)-amides was evaluated at in vitro test on prostate cancer PC-3 cell lines. It is indicated, that at concentration of 10–5 M these compounds exceed 5-fluorouracil as comparison drug in inhibiting PC-3 prostate cancer cells growth by 52.32 % and 3.93 % correspondingly. The data obtained substantiate feasibility of further studies of 1-(41-isopro pylphenyl)-4-(42-chlorophenyl)-5,6,7,8-tetrahydro-2,4а-diazacyclopenta[cd] azulene-2-carboxylic acid arylamides as new, potential antitumor medicines for prostate cancer treatment.
1-(41-异丙基苯基)-4-(42-氯苯基)5,6,7,8-四氢-2,4,4 -二氮杂环五[cd]azulene-2-羧酸芳基酰胺的合成及其对PC-3前列腺癌细胞的抗癌活性
前列腺癌的药物治疗是防治肿瘤疾病的重要组成部分。这是非常相关的,因为前列腺癌是10%的男性癌症死亡的原因。本研究目的是合成1-(41-异丙基苯基)-4-(42-氯苯基)5,6,7,8-四氢-2,4,4 -二氮杂环五[cd] azulen2 -羧酸芳基酰胺的新衍生物,并评价其对PC-3前列腺癌细胞的抗肿瘤活性。以等摩尔量的2-甲氧基-3,4,5,6-四氢- 7h -氮平与a-氨基-4-氯苯乙酮水合物反应,合成了3-(4-氯苯基)-6,7,8,9- tetrahydro-5Н-imidazo[1,2-a]氮平。通过在乙酸乙酯中烷基化a-溴-4- 索丙基乙苯酮,再用过量5%的NaOH溶液处理得到中间季盐,合成了1-(41-异丙基苯基)-4-(42氯苯基)-5,6,7,8-四氢-2,4,4 -二氮杂环五[cd] azulene。将其与等摩尔量的相应芳基异氰酸酯在干燥的苯中煮沸,合成了1-(41-异丙基苯基)-4(42-氯苯基)-5,6,7,8-四氢-2,4,4 -二氮杂环五[cd] azulen2 -羧酸芳基酰胺。所得化合物的结构和纯度均通过MR1Н光谱数据得到证实。用ACD LogP程序计算化合物6和8 a-i的亲脂性(LogP)。研究了1-(41-异丙基苯基)-4-(42-氯苯基)-5,6,7,8-四氢-2,4,1-二氮杂环五[cd] -2-羧酸(3-甲基苯基)和(3-甲氧基苯基)-酰胺对前列腺癌PC-3细胞株的体外抗肿瘤活性。结果表明,在10-5 M浓度下,这些化合物对PC-3前列腺癌细胞的抑制作用分别比5-氟尿嘧啶高52.32%和3.93%。这些数据证实了进一步研究1-(41-异丙基苯基)-4-(42-氯苯基)-5,6,7,8-四氢-2,4,4 -二氮杂环五[cd] azulen2 -羧酸芳基酰胺作为治疗前列腺癌的新型潜在抗肿瘤药物的可行性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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