Covalent inhibitors design and discovery.
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Nicolas Moitessier | A. Mittermaier | Stephane De Cesco | N. Moitessier | C. Dufresne | Caroline Dufresne | Jerry Kurian | Stephane De Cesco | Anthony K Mittermaier | Jerry Kurian
[1] G. Ramesh,et al. Mechanisms of Cisplatin Nephrotoxicity , 2010, Toxins.
[2] Allard Kaptein,et al. Irreversible protein kinase inhibitors: balancing the benefits and risks. , 2012, Journal of medicinal chemistry.
[3] G. S. Walker,et al. Chemical and computational methods for the characterization of covalent reactive groups for the prospective design of irreversible inhibitors. , 2014, Journal of medicinal chemistry.
[4] T. Baillie,et al. Targeted Covalent Inhibitors for Drug Design. , 2016, Angewandte Chemie.
[5] J. Rey,et al. Nouvelle perspective de traitement dans le cancer bronchique non à petites cellules (CBNPC). Place de l’afatinib : un inhibiteur oral et irréversible de la famille ErbB , 2014 .
[6] P. Tonge,et al. Slow-onset inhibition of the FabI enoyl reductase from francisella tularensis: residence time and in vivo activity. , 2009, ACS chemical biology.
[7] Robert A Copeland,et al. The dynamics of drug-target interactions: drug-target residence time and its impact on efficacy and safety , 2010, Expert opinion on drug discovery.
[8] Shuo Zhou,et al. CovalentDock: Automated covalent docking with parameterized covalent linkage energy estimation and molecular geometry constraints , 2013, J. Comput. Chem..
[9] Kai Zhu,et al. Structure-Based Virtual Screening Approach for Discovery of Covalently Bound Ligands , 2014, J. Chem. Inf. Model..
[10] R. Guerciolini. Mode of action of orlistat. , 1997, International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity.
[11] Jean-François Truchon,et al. A generally applicable method for assessing the electrophilicity and reactivity of diverse nitrile-containing compounds. , 2007, Bioorganic & medicinal chemistry letters.
[12] Jack Taunton,et al. Reversible targeting of noncatalytic cysteines with chemically tuned electrophiles , 2012, Nature chemical biology.
[13] Vincent Zoete,et al. On-the-Fly QM/MM Docking with Attracting Cavities , 2017, J. Chem. Inf. Model..
[14] P Willett,et al. Development and validation of a genetic algorithm for flexible docking. , 1997, Journal of molecular biology.
[15] A. Rossi,et al. Erlotinib in non-small cell lung cancer treatment: current status and future development. , 2007, The oncologist.
[16] J. Baell,et al. Chemistry: Chemical con artists foil drug discovery , 2014, Nature.
[17] T. Reid,et al. The scarlet letter of alkylation: a mini review of selective alkylating agents. , 2012, Translational oncology.
[18] Jayme L. Dahlin,et al. How to Triage PAINS-Full Research. , 2016, Assay and drug development technologies.
[19] S. Pascarella,et al. On the mechanism of Escherichia coli pyridoxal kinase inhibition by pyridoxal and pyridoxal 5'-phosphate. , 2015, Biochimica et Biophysica Acta.
[20] Steven J Brown,et al. Identification of selective inhibitors of uncharacterized enzymes by high-throughput screening with fluorescent activity-based probes , 2009, Nature Biotechnology.
[21] B. Cravatt,et al. Activity-based protein profiling for the functional annotation of enzymes , 2007, Nature Methods.
[22] J. Morrison,et al. The slow-binding and slow, tight-binding inhibition of enzyme-catalysed reactions , 1982 .
[23] B. Cravatt,et al. Enzyme inhibitor discovery by activity-based protein profiling. , 2014, Annual review of biochemistry.
[24] A. Monzingo,et al. Characterization of C‐Alkyl Amidines as Bioavailable Covalent Reversible Inhibitors of Human DDAH‐1 , 2011, ChemMedChem.
[25] Wilhelm Huisinga,et al. Mechanism-Based Inhibition: Deriving KI and kinact Directly from Time-Dependent IC50 Values , 2009, Journal of biomolecular screening.
[26] E. Ben-Menachem,et al. Antiepileptic drugs : pharmacology and therapeutics , 1999 .
[27] R. Coletta,et al. The fatty acid synthase inhibitor orlistat reduces experimental metastases and angiogenesis in B16-F10 melanomas , 2012, British Journal of Cancer.
[28] P. Patsalos. Vigabatrin , 1989, The Lancet.
[29] Thomas A. Halgren,et al. Identifying and Characterizing Binding Sites and Assessing Druggability , 2009, J. Chem. Inf. Model..
[30] P. Jänne,et al. Pharmacological Targeting of the Pseudokinase Her3 , 2014, Nature chemical biology.
[31] Alexander Tropsha,et al. Phantom PAINS: Problems with the Utility of Alerts for Pan-Assay INterference CompoundS , 2017, J. Chem. Inf. Model..
[32] B. Cravatt,et al. Strategies for discovering and derisking covalent, irreversible enzyme inhibitors. , 2010, Future medicinal chemistry.
[33] Per Lindberg,et al. A proton-pump inhibitor expedition: the case histories of omeprazole and esomeprazole , 2003, Nature Reviews Drug Discovery.
[34] André Koch,et al. A chemical genetic approach for covalent inhibition of analogue-sensitive aurora kinase. , 2012, ACS chemical biology.
[35] Anna E Speers,et al. Chemical Strategies for Activity‐Based Proteomics , 2004, Chembiochem : a European journal of chemical biology.
[36] Samy O Meroueh,et al. Bacterial resistance to beta-lactam antibiotics: compelling opportunism, compelling opportunity. , 2005, Chemical reviews.
[37] F. Fleming,et al. Nitrile-containing pharmaceuticals: efficacious roles of the nitrile pharmacophore. , 2010, Journal of medicinal chemistry.
[38] Stefano Forli,et al. Covalent docking using autodock: Two‐point attractor and flexible side chain methods , 2016, Protein science : a publication of the Protein Society.
[39] W. Metzler,et al. Mechanism of Gly-Pro-pNA cleavage catalyzed by dipeptidyl peptidase-IV and its inhibition by saxagliptin (BMS-477118). , 2006, Archives of biochemistry and biophysics.
[40] M. Zappalà,et al. Peptide‐Based Proteasome Inhibitors in Anticancer Drug Design , 2014, Medicinal research reviews.
[41] Atsushi B. Tsuji,et al. Fatty Acid Synthase Is a Key Target in Multiple Essential Tumor Functions of Prostate Cancer: Uptake of Radiolabeled Acetate as a Predictor of the Targeted Therapy Outcome , 2013, PloS one.
[42] J. Falgueyret,et al. The discovery of odanacatib (MK-0822), a selective inhibitor of cathepsin K. , 2008, Bioorganic & medicinal chemistry letters.
[43] R. Solé,et al. The topology of drug-target interaction networks: implicit dependence on drug properties and target families. , 2009, Molecular bioSystems.
[44] T. Oki,et al. Epoxomicin, a new antitumor agent of microbial origin. , 1992, The Journal of antibiotics.
[45] Kai Zhu,et al. Docking Covalent Inhibitors: A Parameter Free Approach To Pose Prediction and Scoring , 2014, J. Chem. Inf. Model..
[46] Peter J Tonge,et al. Translating slow-binding inhibition kinetics into cellular and in vivo effects. , 2015, Nature chemical biology.
[47] R. Copeland,et al. Residence time of receptor-ligand complexes and its effect on biological function. , 2008, Biochemistry.
[48] A. Hopkins,et al. Navigating chemical space for biology and medicine , 2004, Nature.
[49] Steven J Brown,et al. Oxime esters as selective, covalent inhibitors of the serine hydrolase retinoblastoma-binding protein 9 (RBBP9). , 2010, Bioorganic & medicinal chemistry letters.
[50] R. Nicholson,et al. The antiepidermal growth factor receptor agent gefitinib (ZD1839/Iressa) improves antihormone response and prevents development of resistance in breast cancer in vitro. , 2003, Endocrinology.
[51] R. Copeland. The drug–target residence time model: a 10-year retrospective , 2015, Nature Reviews Drug Discovery.
[52] Walter Huber,et al. Structural basis of proline-specific exopeptidase activity as observed in human dipeptidyl peptidase-IV. , 2003, Structure.
[53] D. Moro-Sibilot,et al. [A new perspective in the treatment of non-small-cell lung cancer (NSCLC). Role of afatinib: An oral and irreversible ErbB family blocker]. , 2014, Bulletin du cancer.
[54] D. Edmondson,et al. Reversible and irreversible small molecule inhibitors of monoamine oxidase B (MAO-B) investigated by biophysical techniques. , 2015, Bioorganic & medicinal chemistry.
[55] Robert A. Alberty,et al. Application of the Theory of Diffusion-controlled Reactions to Enzyme Kinetics , 1958 .
[56] J. M. Bradshaw,et al. Prolonged and tunable residence time using reversible covalent kinase inhibitors , 2015, Nature chemical biology.
[57] S. Kunapuli,et al. Inactivation of the human P2Y12 receptor by thiol reagents requires interaction with both extracellular cysteine residues, Cys17 and Cys270. , 2003, Blood.
[58] W. Metzler,et al. Involvement of DPP‐IV catalytic residues in enzyme–saxagliptin complex formation , 2008, Protein science : a publication of the Protein Society.
[59] B. Cravatt,et al. Protein-Reactive Natural Products , 2005 .
[60] T. Eble,et al. AN ANTIPHAGE AGENT ISOLATED FROM ASPERGILLUS SP , 1949, Journal of bacteriology.
[61] V. Dembitsky,et al. Boron containing compounds as protease inhibitors. , 2012, Chemical reviews.
[62] C. Mcguigan,et al. Boronic acids in medicinal chemistry: anticancer, antibacterial and antiviral applications , 2010 .
[63] T. Salo,et al. The Fatty Acid Synthase Inhibitor Orlistat Reduces the Growth and Metastasis of Orthotopic Tongue Oral Squamous Cell Carcinomas , 2013, Molecular Cancer Therapeutics.
[64] Pengyu Y. Ren,et al. Reversible Covalent Inhibition of eEF‐2K by Carbonitriles , 2014, Chembiochem : a European journal of chemical biology.
[65] Nicolas Moitessier,et al. Virtual screening and computational optimization for the discovery of covalent prolyl oligopeptidase inhibitors with activity in human cells. , 2012, Journal of medicinal chemistry.
[67] Nir London,et al. Covalent Docking of Large Libraries for the Discovery of Chemical Probes , 2014, Nature chemical biology.
[68] R. Copeland,et al. Drug–target residence time and its implications for lead optimization , 2007, Nature Reviews Drug Discovery.
[69] D. Moras,et al. Cysteine mapping in conformationally distinct kinase nucleotide binding sites: application to the design of selective covalent inhibitors. , 2011, Journal of medicinal chemistry.
[70] R. Baron,et al. Time-dependent inhibition of isoprenylcysteine carboxyl methyltransferase by indole-based small molecules. , 2007, Biochemistry.
[71] Kay Hamacher,et al. DOCKTITE - A Highly Versatile Step-by-Step Workflow for Covalent Docking and Virtual Screening in the Molecular Operating Environment , 2015, J. Chem. Inf. Model..
[72] Andrew G. Leach,et al. Beyond picomolar affinities: quantitative aspects of noncovalent and covalent binding of drugs to proteins. , 2009, Journal of medicinal chemistry.
[73] Nicolas Moitessier,et al. 3-Oxo-hexahydro-1H-isoindole-4-carboxylic Acid as a Drug Chiral Bicyclic Scaffold: Structure-Based Design and Preparation of Conformationally Constrained Covalent and Noncovalent Prolyl Oligopeptidase Inhibitors. , 2016, Journal of medicinal chemistry.
[74] Matthew Bogyo,et al. Using small molecules to dissect mechanisms of microbial pathogenesis. , 2009, ACS chemical biology.
[75] T. Chambers,et al. Recent developments in cathepsin K inhibitor design. , 2005, Current opinion in drug discovery & development.
[76] Taebo Sim,et al. Discovery of potent and selective covalent inhibitors of JNK. , 2012, Chemistry & biology.
[77] S. Sieber,et al. Electrophilic natural products and their biological targets. , 2012, Natural product reports.
[78] John B. Shoven,et al. I , Edinburgh Medical and Surgical Journal.
[79] T. Numata,et al. A Novel Transition-state Analogue for Lysozyme, 4-O-β-Tri-N-acetylchitotriosyl Moranoline, Provided Evidence Supporting the Covalent Glycosyl-enzyme Intermediate* , 2013, The Journal of Biological Chemistry.
[80] W. S. Faraci,et al. Slow tight-binding inhibition of prolyl endopeptidase by benzyloxycarbonyl-prolyl-prolinal. , 1990, The Biochemical journal.
[81] Nicolas Moitessier,et al. Constrained peptidomimetics reveal detailed geometric requirements of covalent prolyl oligopeptidase inhibitors. , 2009, Journal of medicinal chemistry.
[82] A comprehensive review of the preclinical efficacy profile of the ErbB family blocker afatinib in cancer , 2014, Naunyn-Schmiedeberg's Archives of Pharmacology.
[83] Elisabetta Marini,et al. Electrophilic warhead-based design of compounds preventing NLRP3 inflammasome-dependent pyroptosis. , 2014, Journal of medicinal chemistry.
[84] B. Cravatt,et al. Activity-based protein profiling: from enzyme chemistry to proteomic chemistry. , 2008, Annual review of biochemistry.
[85] Steven J Brown,et al. Discovery and optimization of sulfonyl acrylonitriles as selective, covalent inhibitors of protein phosphatase methylesterase-1. , 2011, Journal of medicinal chemistry.
[86] Christopher R. Corbeil,et al. Medicinal Chemistry Projects Requiring Imaginative Structure-Based Drug Design Methods. , 2016, Accounts of chemical research.
[87] L. Pollegioni,et al. High-Throughput Screening Strategy Identifies Allosteric, Covalent Human D-Amino Acid Oxidase Inhibitor , 2015, Journal of biomolecular screening.
[88] M. Meyerson,et al. The T790M mutation in EGFR kinase causes drug resistance by increasing the affinity for ATP , 2008, Proceedings of the National Academy of Sciences.
[89] Stefan Tenzer,et al. Quantum Chemical-Based Protocol for the Rational Design of Covalent Inhibitors. , 2016, Journal of the American Chemical Society.
[90] T. Nakashima,et al. Azinomycins A and B, new antitumor antibiotics. II. Chemical structures. , 1986, Chemical & pharmaceutical bulletin.
[91] A. J. Bennet,et al. A mechanism-based inactivator of glycoside hydrolases involving formation of a transient non-classical carbocation , 2014, Nature Communications.
[92] P. Lindberg,et al. The mechanism of action of the gastric acid secretion inhibitor omeprazole. , 1986, Journal of medicinal chemistry.
[93] D. Swinney,et al. Biochemical Mechanisms of New Molecular Entities (NMEs) approved by United States FDA during 2001‐2004: Mechanisms leading to optimal efficacy and safety. , 2006, Current topics in medicinal chemistry.
[94] J. G. Robertson,et al. Mechanistic basis of enzyme-targeted drugs. , 2005, Biochemistry.
[95] Jennifer M. Smith,et al. Automated computational screening of the thiol reactivity of substituted alkenes , 2015, Journal of Computer-Aided Molecular Design.
[96] P. Janning,et al. Covalent-Allosteric Kinase Inhibitors. , 2015, Angewandte Chemie.
[97] Patricia Hurter,et al. Discovery and development of telaprevir: an NS3-4A protease inhibitor for treating genotype 1 chronic hepatitis C virus , 2011, Nature Biotechnology.
[98] A. Hall,et al. Mechanisms of action of, and modes of resistance to, alkylating agents used in the treatment of haematological malignancies. , 1992, Blood reviews.
[99] T. Beppu,et al. Leptomycins A and B, new antifungal antibiotics. I. Taxonomy of the producing strain and their fermentation, purification and characterization. , 1983, The Journal of antibiotics.
[100] D. Rotella. The discovery and development of boceprevir , 2013, Expert opinion on drug discovery.
[101] Philippe Dumas,et al. kinITC: a new method for obtaining joint thermodynamic and kinetic data by isothermal titration calorimetry. , 2012, Journal of the American Chemical Society.
[102] Gorjan Alagic,et al. #p , 2019, Quantum information & computation.
[103] P. Rasoanaivo,et al. Natural Products and Drug Discovery through a Network of Partnerships , 2006 .
[104] Christopher M Harris,et al. Tricyclic Covalent Inhibitors Selectively Target Jak3 through an Active Site Thiol* , 2014, The Journal of Biological Chemistry.
[105] Christopher R. Corbeil,et al. Towards the development of universal, fast and highly accurate docking/scoring methods: a long way to go , 2008, British journal of pharmacology.
[106] A. Wonacott,et al. Structure of UDP-N-acetylglucosamine enolpyruvyl transferase, an enzyme essential for the synthesis of bacterial peptidoglycan, complexed with substrate UDP-N-acetylglucosamine and the drug fosfomycin. , 1996, Structure.
[107] Markus Hartenfeller,et al. De novo drug design. , 2010, Methods in molecular biology.
[108] Adriaan P IJzerman,et al. Drug‐Target Residence Time—A Case for G Protein‐Coupled Receptors , 2014, Medicinal research reviews.
[109] Yan Wang,et al. Discovery of a series of 2,5-diaminopyrimidine covalent irreversible inhibitors of Bruton's tyrosine kinase with in vivo antitumor activity. , 2014, Journal of medicinal chemistry.
[110] R. Vergona,et al. Novel P2Y12 adenosine diphosphate receptor antagonists for inhibition of platelet aggregation (II): pharmacodynamic and pharmacokinetic characterization. , 2008, Thrombosis research.
[111] Melanie A. Priestman,et al. Evidence That the Fosfomycin Target Cys115 in UDP-N-acetylglucosamine Enolpyruvyl Transferase (MurA) Is Essential for Product Release* , 2005, Journal of Biological Chemistry.
[112] Adrian Whitty,et al. The resurgence of covalent drugs , 2011, Nature Reviews Drug Discovery.
[113] P. Tonge,et al. Drug-target residence time: critical information for lead optimization. , 2010, Current opinion in chemical biology.
[114] J. Schwöbel,et al. Prediction of michael-type acceptor reactivity toward glutathione. , 2010, Chemical research in toxicology.
[115] Soumendranath Bhakat,et al. Theory and Applications of Covalent Docking in Drug Discovery: Merits and Pitfalls , 2015, Molecules.
[116] T. Skarzynski. STRUCTURE OF UDP-N-ACETYLGLUCOSAMINE ENOLPYRUVYL TRANSFERASE , 1997 .
[117] R. A. Bauer. Covalent inhibitors in drug discovery: from accidental discoveries to avoided liabilities and designed therapies. , 2015, Drug discovery today.
[118] M. Wenk,et al. Activity-based proteome profiling of potential cellular targets of Orlistat--an FDA-approved drug with anti-tumor activities. , 2010, Journal of the American Chemical Society.
[119] Walter Huber,et al. Biomolecular interaction analysis in drug discovery using surface plasmon resonance technology. , 2006, Current pharmaceutical design.
[120] Mahmoud E. S. Soliman,et al. Identification of irreversible protein splicing inhibitors as potential anti-TB drugs: insight from hybrid non-covalent/covalent docking virtual screening and molecular dynamics simulations , 2013, Medicinal Chemistry Research.
[121] Harry C. J. Ottenheijm,et al. CASE HISTORIES OF PEPTIDOMIMETICS : PROGRESSION FROM PEPTIDES TO DRUGS , 1994 .
[122] Yingkai Zhang,et al. Mechanistic Insights into a Classic Wonder Drug—Aspirin , 2014, Journal of the American Chemical Society.
[123] David Baker,et al. Quantitative reactivity profiling predicts functional cysteines in proteomes , 2010, Nature.
[124] B. Cravatt,et al. Activity-based protein profiling: the serine hydrolases. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[125] Chin Yee Liew,et al. QSAR classification of metabolic activation of chemicals into covalently reactive species , 2012, Molecular Diversity.
[126] Thomas Lengauer,et al. Evaluation of the FLEXX incremental construction algorithm for protein–ligand docking , 1999, Proteins.
[127] Olivier Sperandio,et al. FAF-Drugs3: a web server for compound property calculation and chemical library design , 2015, Nucleic Acids Res..
[128] M. Shokhen,et al. Differentiating Serine and Cysteine Protease Mechanisms by New Covalent QSAR Descriptors , 2011, Chembiochem : a European journal of chemical biology.