Designing Irreversible InhibitorsWorth the Effort?

被引:60
作者
Gonzalez-Bello, Concepcion [1 ]
机构
[1] Univ Santiago Compostela, Ctr Singular Invest Quim Biol & Mat Mol CIQUS, Santiago De Compostela 15782, Spain
关键词
covalent catalysis; efficiency; irreversible inhibition; selectivity; toxicity; BETA-LACTAMASE INHIBITORS; GASTRIC-ACID SECRETION; PROTON-PUMP INHIBITOR; ACINETOBACTER-BAUMANNII; COVALENT INHIBITORS; KINASE INHIBITORS; ALLOSTERIC INHIBITORS; TARGETING VIRULENCE; DRUG DISCOVERY; OMEPRAZOLE;
D O I
10.1002/cmdc.201500469
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
Despite the unquestionable success of numerous irreversible drugs that are currently in clinical use, such as acetylsalicylic acid (Aspirin) and penicillin, the number of such approved drugs is much lower than that of noncovalent drugs. Over the years, the potential off-target effects of these types of compounds have been the primary concern that has hampered their development. However, their remarkable advantages over noncovalent drugs and a better analysis of the risks have decreased the widespread skepticism surrounding them. The design of irreversible inhibitors is a challenge, particularly considering that in some cases their efficacy is due to complex and unexpected mechanisms of action. In this review the main advantages of irreversible inhibition are summarized, and the complexity of certain covalent modification mechanisms is highlighted with selected examples.
引用
收藏
页码:22 / 30
页数:9
相关论文
共 73 条
[1]
Characterization of OXA-25, OXA-26, and OXA-27, molecular class D β-lactamases associated with carbapenem resistance in clinical isolates of Acinetobacter baumannii [J].
Afzal-Shah, M ;
Woodford, N ;
Livermore, DM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (02) :583-588
[2]
Targeting virulence: can we make evolution-proof drugs? [J].
Allen, Richard C. ;
Popat, Roman ;
Diggle, Stephen P. ;
Brown, Sam P. .
NATURE REVIEWS MICROBIOLOGY, 2014, 12 (04) :300-308
[3]
Covalent Inhibition of Bacterial Quorum Sensing [J].
Amara, Neri ;
Mashiach, Roi ;
Amar, Dotan ;
Krief, Pnina ;
Spieser, Stephane A. H. ;
Bottomley, Matthew J. ;
Aharoni, Amir ;
Meijler, Michael M. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (30) :10610-10619
[4]
Pharmacokinetics and pharmacodynamics of esomeprazole, the S-isomer of omeprazole [J].
Andersson, T ;
Röhss, K ;
Bredberg, E ;
Hassan-Alin, M .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2001, 15 (10) :1563-1569
[5]
Irreversible Protein Kinase Inhibitors: Balancing the Benefits and Risks [J].
Barf, Tjeerd ;
Kaptein, Allard .
JOURNAL OF MEDICINAL CHEMISTRY, 2012, 55 (14) :6243-6262
[6]
Covalent inhibitors in drug discovery: from accidental discoveries to avoided liabilities and designed therapies [J].
Bauer, Renato A. .
DRUG DISCOVERY TODAY, 2015, 20 (09) :1061-1073
[7]
MEMBRANE TOPOLOGY AND OMEPRAZOLE LABELING OF THE GASTRIC H+,K+-ADENOSINE-TRIPHOSPHATASE [J].
BESANCON, M ;
SHIN, JM ;
MERCIER, F ;
MUNSON, K ;
MILLER, M ;
HERSEY, S ;
SACHS, G .
BIOCHEMISTRY, 1993, 32 (09) :2345-2355
[8]
OXA-24, a novel class D β-lactamase with carbapenemase activity in an Acinetobacter baumannii clinical strain [J].
Bou, G ;
Oliver, A ;
Martínez-Beltran, J .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (06) :1556-1561
[9]
Design, Synthesis, and Crystal Structures of 6-Alkylidene-2′-Substituted Penicillanic Acid Sulfones as Potent Inhibitors of Acinetobacter baumannii OXA-24 Carbapenemase [J].
Bou, German ;
Santillana, Elena ;
Sheri, Anjaneyulu ;
Beceiro, Alejandro ;
Sampson, Jared M. ;
Kalp, Matthew ;
Bethel, Christopher R. ;
Distler, Anne M. ;
Drawz, Sarah M. ;
Pagadala, Sundar Ram Reddy ;
van den Akker, Focco ;
Bonomo, Robert A. ;
Romero, Antonio ;
Buynak, John D. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2010, 132 (38) :13320-13331
[10]
Discovery of Covalent Inhibitors of Glyceraldehyde-3-phosphate Dehydrogenase, A Target for the Treatment of Malaria [J].
Bruno, Stefano ;
Pinto, Andrea ;
Paredi, Gianluca ;
Tamborini, Lucia ;
De Micheli, Carlo ;
La Pietra, Valeria ;
Marinelli, Luciana ;
Novellino, Ettore ;
Conti, Paola ;
Mozzarelli, Andrea .
JOURNAL OF MEDICINAL CHEMISTRY, 2014, 57 (17) :7465-7471