An update on β-lactamase inhibitor discovery and development

被引:158
|
作者
Docquier, Jean-Denis [1 ]
Mangani, Stefano [2 ]
机构
[1] Univ Siena, Dept Med Biotechnol, Viale Bracci 16, I-53100 Siena, Italy
[2] Univ Siena, Dept Biotechnol Chem & Pharm, Via Aldo Moro 2, I-53100 Siena, Italy
关键词
Beta-lactamase; Inhibitor; Crystal structure; Antibiotic resistance; Drug discovery; IN-VITRO ACTIVITY; SIDEROPHORE CEPHALOSPORIN CEFIDEROCOL; HIGHLY PROMISING SCAFFOLD; BROAD-SPECTRUM INHIBITION; TRANSITION-STATE ANALOG; GRAM-NEGATIVE BACTERIA; STRUCTURE-BASED DESIGN; CLASS-A; MONOSULFACTAM BAL30072; ANTIMICROBIAL ACTIVITY;
D O I
10.1016/j.drup.2017.11.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Antibiotic resistance, and the emergence of pan-resistant clinical isolates, seriously threatens our capability to treat bacterial diseases, including potentially deadly hospital-acquired infections. This growing issue certainly requires multiple adequate responses, including the improvement of both diagnosis methods and use of antibacterial agents, and obviously the development of novel antibacterial drugs, especially active against Gram-negative pathogens, which represent an urgent medical need. Considering the clinical relevance of both beta-lactam antibiotics and beta-lactamase-mediated resistance, the discovery and development of combinations including a beta-lactamase inhibitor seems to be particularly attractive, despite being extremely challenging due to the enormous diversity, both structurally and mechanistically, of the potential beta-lactamase targets. This review will cover the evolution of currently available beta-lactamase inhibitors along with the most recent research leading to new beta-lactamase inhibitors of potential clinical interest or already in the stage of clinical development.
引用
收藏
页码:13 / 29
页数:17
相关论文
共 50 条
  • [41] Discovery of a new class of β-lactamase inhibitors
    Gonzalez, Janet
    Barquero, Juan
    Clement, Cristina
    Philipp, Manfred
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2016, 251
  • [42] An update on the emerging approaches for histone deacetylase (HDAC) inhibitor drug discovery and future perspectives
    Su, Ma
    Gong, Xingyu
    Liu, Feng
    EXPERT OPINION ON DRUG DISCOVERY, 2021, 16 (07) : 745 - 761
  • [43] Discovery of a Cyclic Boronic Acid β-Lactamase Inhibitor (RPX7009) with Utility vs Class A Serine Carbapenemases
    Hecker, Scott J.
    Reddy, K. Raja
    Totrov, Maxim
    Hirst, Gavin C.
    Lomovskaya, Olga
    Griffith, David C.
    King, Paula
    Tsivkovski, Ruslan
    Sun, Dongxu
    Sabet, Mojgan
    Tarazi, Ziad
    Clifton, Matthew C.
    Atkins, Kateri
    Raymond, Amy
    Potts, Kristy T.
    Abendroth, Jan
    Boyer, Serge H.
    Loutit, Jeffrey S.
    Morgan, Elizabeth E.
    Durso, Stephanie
    Dudley, Michael N.
    JOURNAL OF MEDICINAL CHEMISTRY, 2015, 58 (09) : 3682 - 3692
  • [44] Discovery of a Novel Metallo-β-Lactamase Inhibitor That Potentiates Meropenem Activity against Carbapenem-Resistant Enterobacteriaceae
    Everett, Martin
    Sprynski, Nicolas
    Coelho, Alicia
    Castandet, Jerome
    Bayet, Maelle
    Bougnon, Juliette
    Lozano, Clarisse
    Davies, David T.
    Leiris, Simon
    Zalacain, Magdalena
    Morrissey, Ian
    Magnet, Sophie
    Holden, Kirsty
    Warn, Peter
    De Luca, Filomena
    Docquier, Jean-Denis
    Lemonnier, Marc
    ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2018, 62 (05)
  • [45] Erratum: Discovery and development of sorafenib: a multikinase inhibitor for treating cancer
    Scott Wilhelm
    Christopher Carter
    Mark Lynch
    Timothy Lowinger
    Jacques Dumas
    Roger A. Smith
    Brian Schwartz
    Ronit Simantov
    Susan Kelley
    Nature Reviews Drug Discovery, 2007, 6 : 168 - 168
  • [46] The discovery and development of rivaroxaban, an oral, direct factor Xa inhibitor
    Elisabeth Perzborn
    Susanne Roehrig
    Alexander Straub
    Dagmar Kubitza
    Frank Misselwitz
    Nature Reviews Drug Discovery, 2011, 10 : 61 - 75
  • [47] Discovery of the Novel Inhibitor Against New Delhi Metallo-β-Lactamase Based on Virtual Screening and Molecular Modelling
    Wang, Xiyan
    Yang, Yanan
    Gao, Yawen
    Niu, Xiaodi
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2020, 21 (10)
  • [48] Discovery and development of CC-292, a covalent inhibitor of BTK
    Petter, Russell
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2015, 250
  • [49] Discovery and development of anacetrapib, a potent and orally active CETP inhibitor
    Ali, Amjad
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2012, 243
  • [50] The discovery and development of rivaroxaban, an oral, direct factor Xa inhibitor
    Perzborn, Elisabeth
    Roehrig, Susanne
    Straub, Alexander
    Kubitza, Dagmar
    Misselwitz, Frank
    NATURE REVIEWS DRUG DISCOVERY, 2011, 10 (01) : 61 - +