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苯并咪唑衍生物:寻找对胃肠道友好的抗炎镇痛药

Benzimidazole derivatives: search for GI-friendly anti-inflammatory analgesic agents.

作者信息

Gaba Monika, Gaba Punam, Uppal Deepika, Dhingra Neelima, Bahia Malkeet Singh, Silakari Om, Mohan Chander

机构信息

Department of Pharmaceutical Sciences, ASBASJSM College of Pharmacy, Bela, Ropar, Punjab, India ; Research Scholar, Punjab Technical University, Kapurthala, Punjab, India.

Department of Pharmaceutical Sciences, ASBASJSM College of Pharmacy, Bela, Ropar, Punjab, India.

出版信息

Acta Pharm Sin B. 2015 Jul;5(4):337-42. doi: 10.1016/j.apsb.2015.05.003. Epub 2015 Jun 25.

Abstract

Non-steroidal anti-inflammatory drugs (NSAIDs) have been successfully used for the alleviation of pain and inflammation in the past and continue to be used daily by millions of patients worldwide. However, gastrointestinal (GI) toxicity associated with NSAIDs is an important medical and socioeconomic problem. Local generation of various reactive oxygen species plays a significant role in the formation of gastric ulceration associated with NSAIDs therapy. Co-medication of antioxidants along with NSAIDs has been found to be beneficial in the prevention of GI injury. This paper describes the synthesis and biological evaluation of N-1-(phenylsulfonyl)-2-methylamino-substituted-1H-benzimidazole derivatives as anti-inflammatory analgesic agents with lower GI toxicity. Studies in vitro and in vivo demonstrated that the antioxidant activity of the test compounds decreased GI toxicity.

摘要

非甾体抗炎药(NSAIDs)过去已成功用于缓解疼痛和炎症,并且目前全球仍有数百万患者每天都在使用。然而,与NSAIDs相关的胃肠道(GI)毒性是一个重要的医学和社会经济问题。局部产生的各种活性氧在与NSAIDs治疗相关的胃溃疡形成中起重要作用。已发现抗氧化剂与NSAIDs联合用药对预防胃肠道损伤有益。本文描述了N-1-(苯磺酰基)-2-甲基氨基取代的-1H-苯并咪唑衍生物作为具有较低胃肠道毒性的抗炎镇痛药的合成及生物学评价。体外和体内研究表明,受试化合物的抗氧化活性降低了胃肠道毒性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94e2/4629282/50d0e3e7a0f3/fx1.jpg

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