Preclinical characterization of a water-soluble low-impact ampakine prodrug, CX1942 and its active moiety, CX1763.

IF 3.2 4区 医学 Q3 CHEMISTRY, MEDICINAL
Daniel P Radin, Sheng Zhong, Rok Cerne, Mohammed Shoaib, Jeffrey M Witkin, Arnold Lippa
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引用次数: 0

Abstract

Aim: AMPA-glutamate receptor (AMPAR) dysfunction mediates multiple neurological/neuropsychiatric disorders. Ampakines bind AMPARs and allosterically enhance glutamate-elicited currents. This report describes the activity of the water-soluble ampakine CX1942 prodrug and the active moiety CX1763.Results: CX1763 and CX1942 enhance synaptic transmission in hippocampi of rats. CX1763 increases attention in the 5CSRTT in rats and reduces amphetamine-induced hyperactivity in mice. CX1942 potently reverses opioid-induced respiratory depression in rats. CX1942/CX1763 was effective at 2.5-10 mg/kg. CX1763 lacked epileptogenicity up to 1500 mg/kg in rats.Conclusion: These data document that CX1942 and CX1763 are active and without prominent side effects in multiple pre-clinical assays. CX1942 could serve as a prodrug for CX1763 with the advantage of high water solubility as in an intravenous formulation.

一种水溶性低影响安帕金原药 CX1942 及其活性分子 CX1763 的临床前特征。
目的:AMPA-谷氨酸受体(AMPAR)功能障碍介导多种神经/神经精神疾病。安非他明类药物能与 AMPAR 结合,并通过异体作用增强谷氨酸诱导的电流。本报告介绍了水溶性安帕金 CX1942 原药和活性分子 CX1763 的活性:结果:CX1763 和 CX1942 能增强大鼠海马的突触传递。CX1763 可提高大鼠 5CSRTT 的注意力,减少苯丙胺诱导的小鼠多动症。CX1942 能有效逆转阿片诱导的大鼠呼吸抑制。CX1942/CX1763 的有效剂量为 2.5-10 毫克/千克。CX1763 对大鼠的致痫性可达 1500 毫克/千克:这些数据表明,CX1942 和 CX1763 在多种临床前试验中具有活性,且无明显副作用。CX1942 可作为 CX1763 的原药,在静脉注射制剂中具有高水溶性的优势。
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来源期刊
Future medicinal chemistry
Future medicinal chemistry CHEMISTRY, MEDICINAL-
CiteScore
5.80
自引率
2.40%
发文量
118
审稿时长
4-8 weeks
期刊介绍: Future Medicinal Chemistry offers a forum for the rapid publication of original research and critical reviews of the latest milestones in the field. Strong emphasis is placed on ensuring that the journal stimulates awareness of issues that are anticipated to play an increasingly central role in influencing the future direction of pharmaceutical chemistry. Where relevant, contributions are also actively encouraged on areas as diverse as biotechnology, enzymology, green chemistry, genomics, immunology, materials science, neglected diseases and orphan drugs, pharmacogenomics, proteomics and toxicology.
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