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分子拓扑学在溃疡性结肠炎药物发现中的应用。

The application of molecular topology for ulcerative colitis drug discovery.

作者信息

Bellera Carolina L, Di Ianni Mauricio E, Talevi Alan

机构信息

a Medicinal Chemistry/Laboratory of Bioactive Research and Development, Department of Biological Sciences, Faculty of Exact Sciences , University of La Plata (UNLP) , La Plata , Buenos Aires , Argentina.

出版信息

Expert Opin Drug Discov. 2018 Jan;13(1):89-101. doi: 10.1080/17460441.2018.1396314. Epub 2017 Nov 1.

Abstract

Although the therapeutic arsenal against ulcerative colitis has greatly expanded (including the revolutionary advent of biologics), there remain patients who are refractory to current medications while the safety of the available therapeutics could also be improved. Molecular topology provides a theoretic framework for the discovery of new therapeutic agents in a very efficient manner, and its applications in the field of ulcerative colitis have slowly begun to flourish. Areas covered: After discussing the basics of molecular topology, the authors review QSAR models focusing on validated targets for the treatment of ulcerative colitis, entirely or partially based on topological descriptors. Expert opinion: The application of molecular topology to ulcerative colitis drug discovery is still very limited, and many of the existing reports seem to be strictly theoretic, with no experimental validation or practical applications. Interestingly, mechanism-independent models based on phenotypic responses have recently been reported. Such models are in agreement with the recent interest raised by network pharmacology as a potential solution for complex disorders. These and other similar studies applying molecular topology suggest that some therapeutic categories may present a 'topological pattern' that goes beyond a specific mechanism of action.

摘要

尽管针对溃疡性结肠炎的治疗手段已大幅扩充(包括生物制剂的革命性问世),但仍有患者对现有药物难治,且现有疗法的安全性也有待提高。分子拓扑学以非常高效的方式为新型治疗药物的发现提供了理论框架,其在溃疡性结肠炎领域的应用已开始缓慢兴起。涵盖领域:在讨论分子拓扑学的基础内容后,作者回顾了定量构效关系(QSAR)模型,这些模型完全或部分基于拓扑描述符,聚焦于溃疡性结肠炎治疗的有效靶点。专家观点:分子拓扑学在溃疡性结肠炎药物研发中的应用仍然非常有限,许多现有报告似乎严格来说只是理论性的,没有实验验证或实际应用。有趣的是,最近有基于表型反应的非机制性模型的报道。此类模型与网络药理学作为复杂疾病潜在解决方案所引发的近期关注相一致。这些以及其他应用分子拓扑学的类似研究表明,某些治疗类别可能呈现出超越特定作用机制的“拓扑模式”。

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