个性化文献订阅>期刊> Bioorganic & Medicinal Chemistry Letters
 

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

  作者 Nemmani, KVS; Mali, SV; Borhade, N; Pathan, AR; Karwa, M; Pamidiboina, V; Senthilkumar, SP; Gund, M; Jain, AK; Mangu, NK; Dubash, NP; Desai, DC; Sharma, S; Satyam, A  
  选自 期刊  Bioorganic & Medicinal Chemistry Letters;  卷期  2009年19-18;  页码  5297-5301  
  关联知识点  
 

[摘要]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. (C) 2009 Elsevier Ltd. All rights reserved.

 
      被申请数(0)  
 

[全文传递流程]

一般上传文献全文的时限在1个工作日内