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作为炎症抑制剂的杂环化合物。

Heterocyclic compounds as inflammation inhibitors.

作者信息

Sondhi Sham M, Singhal Nidhi, Johar Monika, Reddy B S Narayan, Lown J William

机构信息

Department of Chemistry, University of Roorkee, Roorkee, 247667, INDIA.

出版信息

Curr Med Chem. 2002 May;9(10):1045-74. doi: 10.2174/0929867024606678.

Abstract

Clinical use of non-steroidal anti-inflammatory drugs (NSAIDs) is associated with significant toxicity particularly in the gastrointestinal tract and kidney. Various approaches such as formulation co-administration (of agents to protect the stomach), chemical manipulation and synthesis of new safer anti-inflammatory drugs reported in the literature to overcome the toxicity of NSAIDs have been summarized. As far as synthesis of new more effective and safer anti-inflammatory drugs is concerned, we have reported recent findings in the area of synthesis of heterocyclic compounds such as pyrimidines, imidazole, benzimidazole, thiazole, thiazolidine, acridine, thiourea, alkanoic acid derivatives and other related heterocyclic compounds and their role as inflammation inhibitors.

摘要

非甾体抗炎药(NSAIDs)的临床应用与显著的毒性相关,尤其是在胃肠道和肾脏方面。文献中报道了各种方法,如(与保护胃的药物)联合制剂、化学操作以及合成新的更安全的抗炎药,以克服NSAIDs的毒性。就合成新的更有效且更安全的抗炎药而言,我们已经报道了在杂环化合物合成领域的最新发现,如嘧啶、咪唑、苯并咪唑、噻唑、噻唑烷、吖啶、硫脲、链烷酸衍生物及其他相关杂环化合物,以及它们作为炎症抑制剂的作用。

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