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二十一世纪的抗生素发现:当前趋势和未来展望。

Antibiotic discovery in the twenty-first century: current trends and future perspectives.

机构信息

NAICONS, Milano, Italy.

出版信息

J Antibiot (Tokyo). 2010 Aug;63(8):423-30. doi: 10.1038/ja.2010.62. Epub 2010 Jun 16.

Abstract

New antibiotics are necessary to treat microbial pathogens that are becoming increasingly resistant to available treatment. Despite the medical need, the number of newly approved drugs continues to decline. We offer an overview of the pipeline for new antibiotics at different stages, from compounds in clinical development to newly discovered chemical classes. Consistent with historical data, the majority of antibiotics under clinical development are natural products or derivatives thereof. However, many of them also represent improved variants of marketed compounds, with the consequent risk of being only partially effective against the prevailing resistance mechanisms. In the discovery arena, instead, compounds with promising activities have been obtained from microbial sources and from chemical modification of antibiotic classes other than those in clinical use. Furthermore, new natural product scaffolds have also been discovered by ingenious screening programs. After providing selected examples, we offer our view on the future of antibiotic discovery.

摘要

需要新的抗生素来治疗对现有治疗方法越来越耐药的微生物病原体。尽管存在医疗需求,但新批准的药物数量仍在持续下降。我们概述了处于不同阶段的新型抗生素的研发管线,从处于临床开发阶段的化合物到新发现的化学类别。与历史数据一致,大多数处于临床开发阶段的抗生素是天然产物或其衍生物。然而,其中许多也是已上市化合物的改良变体,因此可能仅对当前流行的耐药机制部分有效。在发现领域,具有良好活性的化合物则来自微生物来源和临床使用以外的抗生素类别的化学修饰。此外,通过巧妙的筛选计划,也发现了新的天然产物支架。在提供了一些选定的例子后,我们对抗生素发现的未来提出了看法。

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