Covalent inhibitors in drug discovery: from accidental discoveries to avoided liabilities and designed therapies

被引:406
作者
Bauer, Renato A. [1 ]
机构
[1] Eli Lilly & Co, Lilly Res Labs, Indianapolis, IN 46285 USA
关键词
MECHANISM-BASED INHIBITION; TYROSINE KINASE INHIBITOR; BIOCHEMICAL-MECHANISMS; ETHACRYNIC-ACID; BTK INHIBITORS; NEW-GENERATION; ENZYME; PROTEIN; BINDING; PHARMACOLOGY;
D O I
10.1016/j.drudis.2015.05.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Drugs that covalently bond to their biological targets have a long history in drug discovery. A look at drug approvals in recent years suggests that covalent drugs will continue to make impacts on human health for years to come. Although fraught with concerns about toxicity, the high potencies and prolonged effects achievable with covalent drugs may result in less-frequent drug dosing and in wide therapeutic margins for patients. Covalent inhibition can also dissociate drug pharmacodynamics (PD) from pharmacokinetics (PK), which can result in desired drug efficacy for inhibitors that have short systemic exposure. Evidence suggests that there is a reduced risk for the development of resistance against covalent drugs, which is a major challenge in areas such as oncology and infectious disease.
引用
收藏
页码:1061 / 1073
页数:13
相关论文
共 90 条
[1]   Development of the proteasome inhibitor PS-341 [J].
Adams, J .
ONCOLOGIST, 2002, 7 (01) :9-16
[2]   Mechanistic and Pharmacological Characterization of PF-04457845: A Highly Potent and Selective Fatty Acid Amide Hydrolase Inhibitor That Reduces Inflammatory and Noninflammatory Pain [J].
Ahn, Kay ;
Smith, Sarah E. ;
Liimatta, Marya B. ;
Beidler, David ;
Sadagopan, Nalini ;
Dudley, David T. ;
Young, Tim ;
Wren, Paul ;
Zhang, Yanhua ;
Swaney, Steven ;
Van Becelaere, Keri ;
Blankman, Jacqueline L. ;
Nomura, Daniel K. ;
Bhattachar, Shobha N. ;
Stiff, Cory ;
Nomanbhoy, Tyzoon K. ;
Weerapana, Eranthie ;
Johnson, Douglas S. ;
Cravatt, Benjamin F. .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2011, 338 (01) :114-124
[3]   Ibrutinib and novel BTK inhibitors in clinical development [J].
Akinleye, Akintunde ;
Chen, Yamei ;
Mukhi, Nikhil ;
Song, Yongping ;
Liu, Delong .
JOURNAL OF HEMATOLOGY & ONCOLOGY, 2013, 6
[4]  
[Anonymous], 2012, NUTRACEUTICALS CANC
[5]  
Baird IM, 2000, FOOD CHEM TOXICOL, V38, pS123, DOI 10.1016/S0278-6915(00)00035-1
[6]   Irreversible Protein Kinase Inhibitors: Balancing the Benefits and Risks [J].
Barf, Tjeerd ;
Kaptein, Allard .
JOURNAL OF MEDICINAL CHEMISTRY, 2012, 55 (14) :6243-6262
[7]   DPP-4 inhibitors and their potential role in the management of type 2 diabetes [J].
Barnett, A. .
INTERNATIONAL JOURNAL OF CLINICAL PRACTICE, 2006, 60 (11) :1454-1470
[8]  
Bauer RA, 2013, NAT CHEM BIOL, V9, P21, DOI [10.1038/NCHEMBIO.1130, 10.1038/nchembio.1130]
[9]   Mechanism-based inhibition of human steroid 5 alpha-reductase by finasteride: Enzyme-catalyzed formation of NADP-dihydrofinasteride, a potent bisubstrate analog inhibitor [J].
Bull, HG ;
GarciaCalvo, M ;
Andersson, S ;
Baginsky, WF ;
Chan, HK ;
Ellsworth, DE ;
Miller, RR ;
Stearns, RA ;
Bakshi, RK ;
Rasmusson, GH ;
Tolman, RL ;
Myers, RW ;
Kozarich, JW ;
Harris, GS .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (10) :2359-2365
[10]   EFFECT OF ETHACRYNIC-ACID ON THICK ASCENDING LIMB OF HENLES LOOP [J].
BURG, M ;
GREEN, N .
KIDNEY INTERNATIONAL, 1973, 4 (05) :301-308