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[SIPI5047的合成及中枢非阿片类镇痛活性]

[Synthesis and central none-opioid analgesic activity of SIPI5047].

作者信息

Li Jian-Qi, Huang Li-Ying, Chen Xin-Jian, Weng Zhi-Jie, Zhang Chun-Nian

机构信息

Shanghai Institute of Pharmaceutical Industry, Shanghai 200040, China.

出版信息

Yao Xue Xue Bao. 2008 Jun;43(6):611-8.

Abstract

Compound SIPI5047 was synthesize by using piperazine as starting material in five reaction steps, and its central none-opioid analgesic activity was studied. Its analgesic activity, pharmacological mechanism, action type and drug dependence were well studied in vivo and in vitro. The results show that SIPI5047 has potent analgesic activities in vivo, which is quite similar to morphine and also much more powerful than paracetamol. SIPI5047 has no efficacy to reduce fever or inflammation, but has an obvious action on central nervous system. SIPI5057 has no apparent affinity with the mu-receptor and it is an antagonist that acts on the polyamine site of the NMDA receptor. SIPI5057 appears no drug dependence. SIPI5047 is a novel central none-opioid analgesic agent and more worthy of further research as a new drug candidate.

摘要

以哌嗪为起始原料,经五步反应合成了化合物SIPI5047,并对其中枢非阿片类镇痛活性进行了研究。在体内和体外对其镇痛活性、药理机制、作用类型和药物依赖性进行了深入研究。结果表明,SIPI5047在体内具有强大的镇痛活性,与吗啡相当,且比扑热息痛强得多。SIPI5047无退热或抗炎作用,但对中枢神经系统有明显作用。SIPI5057与μ受体无明显亲和力,是一种作用于NMDA受体多胺位点的拮抗剂。SIPI5057未表现出药物依赖性。SIPI5047是一种新型的中枢非阿片类镇痛药,作为一种新药候选物更值得进一步研究。

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