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非甾体抗炎药的一氧化氮释放型胃保护前药:无NSAIDs类药物

NO-NSAIDs: Gastric-sparing nitric oxide-releasable prodrugs of non-steroidal anti-inflammatory drugs.

作者信息

Nemmani Kumar V S, Mali Sunil V, Borhade Namdev, Pathan Asif R, Karwa Manoj, Pamidiboina Venu, Senthilkumar S P, Gund Machhindra, Jain Arun K, Mangu Naveen K, Dubash Nauzer P, Desai Dattatraya C, Sharma Somesh, Satyam Apparao

机构信息

Pharmacology Department, Piramal Life Sciences Limited, Nirlon Complex, Goregaon East, Mumbai 400 063, India.

出版信息

Bioorg Med Chem Lett. 2009 Sep 15;19(18):5297-301. doi: 10.1016/j.bmcl.2009.07.142. Epub 2009 Aug 3.

Abstract

Recently, a new class of nitric-oxide-releasing non-steroidal anti-inflammatory drugs (NO-NSAIDs) is being studied as 'Safe NSAIDs' because of their gastric-sparing properties. As an extension of our novel disulfide linker technology, we have designed, synthesized and evaluated novel NO-releasing NSAID prodrugs such as NO-Aspirin (1b-d) and NO-Diclofenac (2b-c). Although the amide-containing derivative 1d did not show any bioavailability, the remaining compounds have shown fair to excellent pharmacokinetic, anti-inflammatory and gastric-sparing properties. Among them, however, the NO-Diclofenac (2b) has shown the most promising pharmacokinetic, anti-inflammatory and NO-releasing properties and protected rats from NSAID-induced gastric damage which could be attributable to the beneficial effects of NO released from these prodrugs.

摘要

最近,一类新型的释放一氧化氮的非甾体抗炎药(NO-NSAIDs)因其具有保护胃的特性而作为“安全的NSAIDs”正在被研究。作为我们新型二硫键连接技术的延伸,我们设计、合成并评估了新型的释放NO的NSAID前药,如NO-阿司匹林(1b-d)和NO-双氯芬酸(2b-c)。尽管含酰胺的衍生物1d没有显示出任何生物利用度,但其余化合物已显示出良好至优异的药代动力学、抗炎和保护胃的特性。然而,其中NO-双氯芬酸(2b)已显示出最有前景的药代动力学、抗炎和释放NO的特性,并保护大鼠免受NSAID诱导的胃损伤,这可能归因于这些前药释放的NO的有益作用。

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