Multitarget ligands in antibacterial research: progress and opportunities

被引:53
作者
East, Stephen P. [1 ]
Silver, Lynn L. [2 ]
机构
[1] Evotec UK Ltd, Abingdon OX14 4SA, Oxon, England
[2] LL Silver Consulting LLC, Springfield, NJ 07081 USA
关键词
antibacterials; bacterial topoisomerases; cell wall biosynthesis; multitarget inhibitors; resistance; structure-based drug design; BACTERIAL TOPOISOMERASE INHIBITORS; DESIGNED MULTIPLE LIGANDS; DNA GYRASE; DRUG DISCOVERY; STAPHYLOCOCCUS-AUREUS; IIA TOPOISOMERASES; UREA INHIBITORS; CELL-WALL; AGENTS; RESISTANCE;
D O I
10.1517/17460441.2013.743991
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Resistance to current antibacterial therapies is an inevitability that represents a significant global health concern. Bacteria have the capacity to render all current drug treatments ineffective, which places a demand on the drug discovery community to constantly develop new antibacterial agents. Compounds that inhibit multiple biological targets, often referred to as multitarget ligands, are an inviting prospect in antibacterial research because, although they will not solve the issue of resistance, they might help to delay the onset. Areas covered: This review covers some of the recent progress in identifying new ligands that deliberately interact with more than one essential biological target in bacteria. The two principal areas covered are inhibitors of DNA replication and cell wall biosynthesis. Expert opinion: Antibacterial programs for the design of multitarget ligands present an important opportunity for production of antibacterial agents. Their longevity, due to slow development of resistance, is comparable to that seen with other successful agents - but is much improved over single-targeted agents for which resistance can appear in vitro overnight. The preclinical development of these agents will have to overcome the standard problems of antibacterial discovery. Such problems include optimization of characteristics favoring cell entry and particularly the demonstration of selectivity of inhibition of the desired multiple targets without inhibition of other bacterial or any mammalian functions.
引用
收藏
页码:143 / 156
页数:14
相关论文
共 75 条
[1]   Development of DNA polymerase IIIC inhibitors for the treatment of gram-positive bacterial infections [J].
Ali, A ;
Taylor, GE .
EXPERT OPINION ON THERAPEUTIC PATENTS, 2005, 15 (08) :947-953
[2]   A New DNA Gyrase Inhibitor Subclass of the Cyclothialidine Family Based on a Bicyclic Dilactam-Lactone Scaffold. Synthesis and Antibacterial Properties [J].
Angehrn, Peter ;
Goetschi, Erwin ;
Gmuender, Hans ;
Hebeisen, Paul ;
Hennig, Michael ;
Kuhn, Bernd ;
Luebbers, Thomas ;
Reindl, Peter ;
Ricklin, Fabienne ;
Schmitt-Hoffmann, Anne .
JOURNAL OF MEDICINAL CHEMISTRY, 2011, 54 (07) :2207-2224
[3]  
[Anonymous], 2012, Achaogen announces all objectives met in Phase 2 plazomicin complicated urinary tract infections study and start of first-in-human study with ACHN-975, Patent No. 201204487
[4]   Toprim - a conserved catalytic domain in type IA and II topoisomerases, DnaG-type primases, OLD family nucleases and RecR proteins [J].
Aravind, L ;
Leipe, DD ;
Koonin, EV .
NUCLEIC ACIDS RESEARCH, 1998, 26 (18) :4205-4213
[5]   New Substructure Filters for Removal of Pan Assay Interference Compounds (PAINS) from Screening Libraries and for Their Exclusion in Bioassays [J].
Baell, Jonathan B. ;
Holloway, Georgina A. .
JOURNAL OF MEDICINAL CHEMISTRY, 2010, 53 (07) :2719-2740
[6]   Type IIA topoisomerase inhibition by a new class of antibacterial agents [J].
Bax, Benjamin D. ;
Chan, Pan F. ;
Eggleston, Drake S. ;
Fosberry, Andrew ;
Gentry, Daniel R. ;
Gorrec, Fabrice ;
Giordano, Ilaria ;
Hann, Michael M. ;
Hennessy, Alan ;
Hibbs, Martin ;
Huang, Jianzhong ;
Jones, Emma ;
Jones, Jo ;
Brown, Kristin Koretke ;
Lewis, Ceri J. ;
May, Earl W. ;
Saunders, Martin R. ;
Singh, Onkar ;
Spitzfaden, Claus E. ;
Shen, Carol ;
Shillings, Anthony ;
Theobald, Andrew J. ;
Wohlkonig, Alexandre ;
Pearson, Neil D. ;
Gwynn, Michael N. .
NATURE, 2010, 466 (7309) :935-U51
[7]   Crystal structure of the anthrax drug target, bacillus anthracis dihydrofolate reductase [J].
Bennett, Brad C. ;
Xu, Hai ;
Simmerman, Richard F. ;
Lee, Richard E. ;
Dealwis, Chris G. .
JOURNAL OF MEDICINAL CHEMISTRY, 2007, 50 (18) :4374-4381
[8]   Mechanism of action of the antibiotic NXL101, a novel nonfluoroquinolone inhibitor of bacterial type II topoisomerases [J].
Black, Michael T. ;
Stachyra, Therese ;
Platel, Denis ;
Girard, Anne-Marie ;
Claudon, Monique ;
Bruneau, Jean-Michel ;
Miossec, Christine .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2008, 52 (09) :3339-3349
[9]   Novel inhibitors of DNA gyrase: 3D structure based biased needle screening, hit validation by biophysical methods, and 3D guided optimization. A promising alternative to random screening [J].
Boehm, HJ ;
Boehringer, M ;
Bur, D ;
Gmuender, H ;
Huber, W ;
Klaus, W ;
Kostrewa, D ;
Kuehne, H ;
Luebbers, T ;
Meunier-Keller, N .
JOURNAL OF MEDICINAL CHEMISTRY, 2000, 43 (14) :2664-2674
[10]   Bacterial cell wall assembly: still an attractive antibacterial target [J].
Bugg, Timothy D. H. ;
Braddick, Darren ;
Dowson, Christopher G. ;
Roper, David I. .
TRENDS IN BIOTECHNOLOGY, 2011, 29 (04) :167-173