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苯丝氨酸(Axonyx/美国国立卫生研究院)

Phenserine (Axonyx/NIH).

作者信息

Thatte U

机构信息

Department of Pharmacology and Therapeutics, Seth GS Medical College, Parel, Mumbai 400 012, India.

出版信息

IDrugs. 2000 Oct;3(10):1222-8.

Abstract

The National Institute on Aging (part of the National Institutes of Health) and Axonyx are investigating phenserine, a phenylcarbamate derivative of physostigmine, as a potential therapy for Alzheimer's disease (AD). The first phase I trial has been completed and, pending the results of a second phase Ib multiple dose study, a phase II efficacy study is scheduled for the fourth quarter of 2000 with completion expected during 2001. Axonyx filed an IND in 1998, which was approved in November 1999, and the company began phase I trials in December 1999 in the US. A second phase I trial, in a group of healthy, elderly volunteers, was initiated in February 2000. Phenserine reduces the production of the amyloid precursor protein and beta-amyloid in vitro. When added to human neuronal cells, Phenserine decreased the production of beta-amyloid peptide by 30%. Phenserine also showed small, non dose-dependent effects on learning in studies in aged rats and lower toxicity than physostigmine. Phenserine has a long duration of action (t(1/2) = 8 to 10 h).

摘要

美国国立衰老研究所(美国国立卫生研究院的一部分)与Axonyx公司正在研究毒扁豆碱的苯基氨基甲酸酯衍生物苯丝氨酸,将其作为治疗阿尔茨海默病(AD)的一种潜在疗法。一期试验已完成,在等待二期Ib多剂量研究结果期间,二期疗效研究计划于2000年第四季度开展,预计在2001年完成。Axonyx公司于1998年提交了研究性新药申请(IND),该申请于1999年11月获批,公司于1999年12月在美国开始一期试验。2000年2月,针对一组健康老年志愿者启动了第二项一期试验。苯丝氨酸在体外可减少淀粉样前体蛋白和β-淀粉样蛋白的产生。当添加到人类神经元细胞中时,苯丝氨酸可使β-淀粉样肽的产生减少30%。在老年大鼠研究中,苯丝氨酸对学习能力也显示出轻微的、非剂量依赖性的影响,且毒性低于毒扁豆碱。苯丝氨酸作用持续时间长(t(1/2)=8至10小时)。

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