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β-内酰胺类抗生素:从药物化学角度综述。

β-lactam antibiotics: An overview from a medicinal chemistry perspective.

机构信息

Instituto Nacional de Ciência e Tecnologia de Fármacos e Medicamentos (INCT-INOFAR), Universidade Federal Do Rio de Janeiro, Laboratório de Avaliação e Síntese de Substâncias Bioativas (LASSBio®), CCS, Cidade Universitária, P.O. Box 68024, ZIP: 21941-971, Rio de Janeiro, RJ, Brazil.

出版信息

Eur J Med Chem. 2020 Dec 15;208:112829. doi: 10.1016/j.ejmech.2020.112829. Epub 2020 Sep 16.

Abstract

β-Lactam antibiotics are one of the most relevant drug classes of antibacterial agents worldwide. The discovery and the market of first β-lactam antibiotic (Penicillin G) is a symbolic landmark of modern chemotherapy. Since then, several other β-lactam antibiotics have been introduced in the therapy, revolutionizing the treatment of bacterial infections. Their antibacterial efficacy has been kept in check by the emergence of bacterial resistance. Among the resistance mechanisms, the expression of β-lactamase enzymes is one of the most studied and prevalent. The combined use of beta-lactamase inhibitors with broad spectrum activity β-lactam antibiotics has been an effective strategy to circumvent the resistance issue. This review discusses, with a focus on structural aspects, the different classes of beta-lactam antibiotics (penicillins, cephalosporins, carbapenems, monobactams and penems) in light of their stability, sensitivity to β-lactamases, mechanism of action and spectrum of antimicrobial activity. β-Lactamase inhibitors (structurally correlated and non-correlated to the β-lactam system) and their proposed inhibition mechanisms are also discussed.

摘要

β-内酰胺类抗生素是全球最重要的抗菌药物类别之一。第一个β-内酰胺类抗生素(青霉素 G)的发现和上市是现代化疗的一个标志性里程碑。此后,又有几种其他的β-内酰胺类抗生素被引入治疗中,彻底改变了细菌感染的治疗方法。然而,细菌耐药性的出现限制了它们的抗菌效果。在这些耐药机制中,β-内酰胺酶的表达是研究和流行最广泛的机制之一。β-内酰胺酶抑制剂与广谱活性的β-内酰胺类抗生素联合使用是克服耐药问题的有效策略。本文主要从结构方面讨论了不同类别的β-内酰胺类抗生素(青霉素类、头孢菌素类、碳青霉烯类、单环β-内酰胺类和碳青霉烯类),包括它们的稳定性、对β-内酰胺酶的敏感性、作用机制和抗菌谱。还讨论了β-内酰胺酶抑制剂(与β-内酰胺系统结构相关和不相关)及其提出的抑制机制。

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