含胺的舒林酸类似物预防癌症。

Q2 Pharmacology, Toxicology and Pharmaceutics Open Medicinal Chemistry Journal Pub Date : 2018-01-31 eCollection Date: 2018-01-01 DOI:10.2174/1874104501812010001
Bini Mathew, Judith V Hobrath, Michele C Connelly, R Kiplin Guy, Robert C Reynolds
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引用次数: 2

摘要

背景:舒林达克属于化学成分多样的非甾体抗炎药(NSAIDs)家族,可有效预防腺瘤性结直肠息肉和结肠癌,特别是对家族性腺瘤性息肉病患者。Sulindac sulfide amide (SSA)是Sulindac sulfide的酰胺类似物,在体外增强抗癌活性并在体内表现出异种移植物活性的同时,显示出不明显的cox相关活性和毒性。目的:建立舒林达胺系列化合物的构效关系,并鉴定具有抗癌活性的类似物。方法:设计合成一系列磺林达克胺类似物,采用“从库到库”的方法进行修饰,得到酰胺类、磺胺类和N,N-二取代的磺林达克胺亚库。所有类似物都对三种癌细胞系(前列腺癌、结肠癌和乳腺癌)进行了筛选。结果:在体外癌细胞筛选中发现了几种有效化合物,其中最有效的化合物(26)在纳摩尔范围内。结论:化合物26及其类似物具有较强的抑制活性,可作为抗肿瘤靶向支架进行进一步的设计和优化。
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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Amine Containing Analogs of Sulindac for Cancer Prevention.

Background: Sulindac belongs to the chemically diverse family of Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) that effectively prevent adenomatous colorectal polyps and colon cancer, especially in patients with familial adenomatous polyposis. Sulindac sulfide amide (SSA), an amide analog of sulindac sulfide, shows insignificant COX-related activity and toxicity while enhancing anticancer activity in vitro and demonstrating in vivo xenograft activity.

Objective: Develop structure-activity relationships in the sulindac amine series and identify analogs with promising anticancer activities.

Method: A series of sulindac amine analogs were designed and synthesized and then further modified in a "libraries from libraries" approach to produce amide, sulfonamide and N,N-disubstituted sulindac amine sub-libraries. All analogs were screened against three cancer cell lines (prostate, colon and breast).

Results: Several active compounds were identified viain vitro cancer cell line screening with the most potent compound (26) in the nanomolar range.

Conclusion: Compound 26 and analogs showing the most potent inhibitory activity may be considered for further design and optimization efforts as anticancer hit scaffolds.

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来源期刊
Open Medicinal Chemistry Journal
Open Medicinal Chemistry Journal Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
4.40
自引率
0.00%
发文量
4
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