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1,2-苯并异恶唑:一种具有多药理学潜力的优势结构。

1, 2-Benzisoxazole: A Privileged Structure with a Potential for Polypharmacology.

作者信息

Uto Yoshikazu

机构信息

Venture Science Laboratories, Daiichi Sankyo Co., Ltd., 1-2-58 Hiromachi, Shinagawa-ku, Tokyo 140- 8710, Japan.

出版信息

Curr Pharm Des. 2016;22(21):3201-11. doi: 10.2174/1381612822666160224142648.

DOI:10.2174/1381612822666160224142648
PMID:26907942
Abstract

BACKGROUND

Privileged structures are potentially able to bind to a diverse range of biologically important proteins with high affinities, thus benefiting the discovery of novel bioactive compounds. 1,2-Benxisoxazole derivatives can be such important types of "privileged structures" possessing a rich diversity of biological properties especially in the area of CNS disorders.

METHODS

This review seeks to explore the most significant examples of 1,2-benzisoxazoles as privileged structures in terms of polypharmacology at the molecular level, specifically focusing on four 1,2-benzisoxazoles (zonisamide, risperidone, paliperidone, and iloperidone) which have been in clinical use and established as effective therapeutics. Furthermore, an updated and detailed account of the pharmacological properties of 1,2-benzisoxazole derivatives as therapeutics for CNS disorders is described. And finally, outlooks on current issues and future directions in this field are also provided.

RESULTS

1,2-Benzisoxazole was successfully employed in the discovery and development of zonisamide for the treatment of epilepsy and Parkinson's disease. 1,2- Benzisoxazole is also a significantly important structure for the development of atypical antipsychotics.

CONCLUSION

It is very reasonable to say that 1,2-benzisoxazole is a good example of a privileged structure because it forms the centerpiece of small molecule chemical entities with a wide range of pharmacological properties, especially in the area of CNS disorders.

摘要

背景

优势结构有可能以高亲和力与多种具有生物学重要性的蛋白质结合,从而有助于发现新型生物活性化合物。1,2-苯并异恶唑衍生物可能是这类重要的“优势结构”,具有丰富多样的生物学特性,尤其是在中枢神经系统疾病领域。

方法

本综述旨在从分子水平的多药理学角度探索1,2-苯并异恶唑作为优势结构的最重要实例,特别关注四种已在临床使用并被确认为有效治疗药物的1,2-苯并异恶唑(唑尼沙胺、利培酮、帕利哌酮和伊潘立酮)。此外,还描述了1,2-苯并异恶唑衍生物作为中枢神经系统疾病治疗药物的药理特性的最新详细情况。最后,还展望了该领域当前的问题和未来的方向。

结果

1,2-苯并异恶唑成功应用于唑尼沙胺的发现和开发,用于治疗癫痫和帕金森病。1,2-苯并异恶唑对于非典型抗精神病药物的开发也是一个非常重要的结构。

结论

可以非常合理地说,1,2-苯并异恶唑是优势结构的一个很好的例子,因为它构成了具有广泛药理特性的小分子化学实体的核心,尤其是在中枢神经系统疾病领域。

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