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Endomorphin-1 analogs with enhanced metabolic stability and systemic analgesic activity: Design, synthesis, and pharmacological characterization

机译:具有增强的代谢稳定性和全身止痛活性的Endomorphin-1类似物:设计,合成和药理学表征

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摘要

We synthesized four new analogs of endomorphin-1 by systematic chemical modifications. To identify the best possible drug candidates for clinical pain management and to investigate the potential contribution of these alterations to the biological activity, their pharmacological properties were determined. All of the analogs showed significantly enhanced metabolic stability. The fact that centrally mediated analgesia following peripheral administration was observed with one of the analogs suggested the approach design undertaken here had validity in the development of endomorphin-1 as a successful opioid drug for the clinic.
机译:我们通过系统的化学修饰合成了四种内啡肽-1新类似物。为了确定用于临床疼痛治疗的最佳候选药物并调查这些改变对生物活性的潜在贡献,确定了它们的药理特性。所有类似物均显示出明显增强的代谢稳定性。使用类似物之一观察到外周给药后发生的中枢性镇痛的事实表明,此处进行的方法设计在开发吗啡肽-1作为临床上成功的阿片类药物方面具有有效性。

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