Type II kinase inhibitors: an opportunity in cancer for rational design.
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[1] Allan Wissner,et al. Kinase domain mutations in cancer: implications for small molecule drug design strategies. , 2009, Journal of medicinal chemistry.
[2] Allard Kaptein,et al. Irreversible protein kinase inhibitors: balancing the benefits and risks. , 2012, Journal of medicinal chemistry.
[3] T. Niwa,et al. Design and synthesis of 3-substituted benzamide derivatives as Bcr-Abl kinase inhibitors. , 2006, Bioorganic & medicinal chemistry letters.
[4] James D. Griffin,et al. Discovery of a small-molecule type II inhibitor of wild-type and gatekeeper mutants of BCR-ABL, PDGFRalpha, Kit, and Src kinases: novel type II inhibitor of gatekeeper mutants. , 2010, Blood.
[5] N. Gray,et al. Targeting cancer with small molecule kinase inhibitors , 2009, Nature Reviews Cancer.
[6] A. Ardavanis,et al. Cardiotoxicity induced by tyrosine kinase inhibitors , 2009, Acta oncologica.
[7] P. N. Rao,et al. Clinical Resistance to STI-571 Cancer Therapy Caused by BCR-ABL Gene Mutation or Amplification , 2001, Science.
[8] John Kuriyan,et al. Crystal structures of the kinase domain of c-Abl in complex with the small molecule inhibitors PD173955 and imatinib (STI-571). , 2001, Cancer research.
[9] J. Mestan,et al. Anthranilic acid amides: a novel class of antiangiogenic VEGF receptor kinase inhibitors. , 2002, Journal of medicinal chemistry.
[10] T. Clackson,et al. Structural Mechanism of the Pan‐BCR‐ABL Inhibitor Ponatinib (AP24534): Lessons for Overcoming Kinase Inhibitor Resistance , 2011, Chemical biology & drug design.
[11] P. Seeburg,et al. Structural mechanism for STI-571 inhibition of abelson tyrosine kinase. , 2000, Science.
[12] Juswinder Singh,et al. Targeted covalent drugs of the kinase family. , 2010, Current opinion in chemical biology.
[13] A. Coxon,et al. Discovery of N-phenyl nicotinamides as potent inhibitors of Kdr. , 2007, Bioorganic & medicinal chemistry letters.
[14] M. Zucchetti,et al. Role of (cid:1) 1 Acid Glycoprotein in the In Vivo Resistance of Human BCR-ABL + Leukemic Cells to the Abl Inhibitor STI571 , 2000 .
[15] M. Gleeson. Generation of a set of simple, interpretable ADMET rules of thumb. , 2008, Journal of medicinal chemistry.
[16] Richard B. Silverman,et al. The Organic Chemistry of Drug Design and Drug Action , 1992 .
[17] K. Gumireddy,et al. A non-ATP-competitive inhibitor of BCR-ABL overrides imatinib resistance. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[18] R. Eglen,et al. Drug discovery and the human kinome: recent trends. , 2011, Pharmacology & therapeutics.
[19] C. Pargellis,et al. The kinetics of binding to p38MAP kinase by analogues of BIRB 796. , 2003, Bioorganic & medicinal chemistry letters.
[20] M. Shibuya,et al. Anti‐tumor activity and tumor vessel normalization by the vascular endothelial growth factor receptor tyrosine kinase inhibitor KRN951 in a rat peritoneal disseminated tumor model , 2008, Cancer science.
[21] N. Gray,et al. Broad spectrum alkynyl inhibitors of T315I Bcr-Abl. , 2010, Bioorganic & medicinal chemistry letters.
[22] B. Hasinoff. The cardiotoxicity and myocyte damage caused by small molecule anticancer tyrosine kinase inhibitors is correlated with lack of target specificity. , 2010, Toxicology and applied pharmacology.
[23] G. Ehninger,et al. P-glycoprotein-mediated drug efflux is a resistance mechanism of chronic myelogenous leukemia cells to treatment with imatinib mesylate , 2004, Leukemia.
[24] F. Lombardo,et al. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings , 1997 .
[25] T. Clackson,et al. Novel N9-arenethenyl purines as potent dual Src/Abl tyrosine kinase inhibitors. , 2008, Bioorganic & medicinal chemistry letters.
[26] Christopher Hulme,et al. The design, synthesis, and evaluation of 8 hybrid DFG-out allosteric kinase inhibitors: a structural analysis of the binding interactions of Gleevec, Nexavar, and BIRB-796. , 2010, Bioorganic & medicinal chemistry.
[27] Abran Q. Costales,et al. Design and synthesis of 5,6-fused heterocyclic amides as Raf kinase inhibitors. , 2011, Bioorganic & medicinal chemistry letters.
[28] F. Giles,et al. Nilotinib: optimal therapy for patients with chronic myeloid leukemia and resistance or intolerance to imatinib , 2009, Drug design, development and therapy.
[29] C. Grütter,et al. Hybrid compound design to overcome the gatekeeper T338M mutation in cSrc. , 2009, Journal of medicinal chemistry.
[30] J. Mestan,et al. In vitro activity of Bcr-Abl inhibitors AMN107 and BMS-354825 against clinically relevant imatinib-resistant Abl kinase domain mutants. , 2005, Cancer research.
[31] T. Hambley,et al. Targeted cancer therapeutics. , 2009, Cancer research.
[32] J. Pollard,et al. Discovery and development of aurora kinase inhibitors as anticancer agents. , 2009, Journal of medicinal chemistry.
[33] Wolfgang Jahnke,et al. Solution Conformations and Dynamics of ABL Kinase-Inhibitor Complexes Determined by NMR Substantiate the Different Binding Modes of Imatinib/Nilotinib and Dasatinib*♦ , 2008, Journal of Biological Chemistry.
[34] N. Gray,et al. Rational design of inhibitors that bind to inactive kinase conformations , 2006, Nature chemical biology.
[35] M. Baccarani,et al. Dual tyrosine kinase inhibitors in chronic myeloid leukemia , 2005, Leukemia.
[36] L. Stewart,et al. Conformational control inhibition of the BCR-ABL1 tyrosine kinase, including the gatekeeper T315I mutant, by the switch-control inhibitor DCC-2036. , 2011, Cancer cell.
[37] 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.
[38] Yasunari Fujiwara,et al. KRN951, a highly potent inhibitor of vascular endothelial growth factor receptor tyrosine kinases, has antitumor activities and affects functional vascular properties. , 2006, Cancer research.
[39] D. Zopf,et al. Regorafenib (BAY 73‐4506): A new oral multikinase inhibitor of angiogenic, stromal and oncogenic receptor tyrosine kinases with potent preclinical antitumor activity , 2011, International journal of cancer.
[40] W. Sippl,et al. Masitinib (AB1010), a Potent and Selective Tyrosine Kinase Inhibitor Targeting KIT , 2009, PloS one.
[41] Paul Reichert,et al. Crystal structures of MEK1 binary and ternary complexes with nucleotides and inhibitors. , 2009, Biochemistry.
[42] D. Ullmann,et al. HTS reporter displacement assay for fragment screening and fragment evolution toward leads with optimized binding kinetics, binding selectivity, and thermodynamic signature. , 2011, Methods in enzymology.
[43] L. Tong,et al. Inhibition of p38 MAP kinase by utilizing a novel allosteric binding site , 2002, Nature Structural Biology.
[44] Keith Abe,et al. Identification of orally active, potent, and selective 4-piperazinylquinazolines as antagonists of the platelet-derived growth factor receptor tyrosine kinase family. , 2002, Journal of medicinal chemistry.
[45] J. Mestan,et al. AMN107 (nilotinib): a novel and selective inhibitor of BCR-ABL , 2006, British Journal of Cancer.
[46] T. Clackson,et al. AP24534, a pan-BCR-ABL inhibitor for chronic myeloid leukemia, potently inhibits the T315I mutant and overcomes mutation-based resistance. , 2009, Cancer cell.
[47] J. Mestan,et al. Urea derivatives of STI571 as inhibitors of Bcr-Abl and PDGFR kinases. , 2004, Bioorganic & medicinal chemistry letters.
[48] John Kuriyan,et al. Equally potent inhibition of c-Src and Abl by compounds that recognize inactive kinase conformations. , 2009, Cancer research.
[49] B. Druker,et al. The ABL switch control inhibitor DCC-2036 is active against the chronic myeloid leukemia mutant BCR-ABLT315I and exhibits a narrow resistance profile. , 2011, Cancer research.
[50] Joon-Oh Park,et al. MET Amplification Leads to Gefitinib Resistance in Lung Cancer by Activating ERBB3 Signaling , 2007, Science.
[51] Adrian Whitty,et al. The resurgence of covalent drugs , 2011, Nature Reviews Drug Discovery.
[52] John T. Powers,et al. Targeting Bcr–Abl by combining allosteric with ATP-binding-site inhibitors , 2010, Nature.
[53] Gabriele Bergers,et al. Modes of resistance to anti-angiogenic therapy , 2008, Nature Reviews Cancer.
[54] H. Kantarjian,et al. Practical advice for determining the role of BCR‐ABL mutations in guiding tyrosine kinase inhibitor therapy in patients with chronic myeloid leukemia , 2011, Cancer.
[55] M. Wittekind,et al. The structure of Dasatinib (BMS-354825) bound to activated ABL kinase domain elucidates its inhibitory activity against imatinib-resistant ABL mutants. , 2006, Cancer research.
[56] E. Casale,et al. Through the "gatekeeper door": exploiting the active kinase conformation. , 2010, Journal of medicinal chemistry.
[57] R. Engh,et al. FMS-like tyrosine kinase 3-internal tandem duplication tyrosine kinase inhibitors display a nonoverlapping profile of resistance mutations in vitro. , 2009, Cancer research.
[58] J. Mestan,et al. Allosteric inhibitors of Bcr-abl–dependent cell proliferation , 2006, Nature chemical biology.
[59] Nanxin Li,et al. Discovery of GNF-5837, a Selective TRK Inhibitor with Efficacy in Rodent Cancer Tumor Models. , 2012, ACS medicinal chemistry letters.
[60] K. Glaser,et al. Discovery of N-(4-(3-amino-1H-indazol-4-yl)phenyl)-N'-(2-fluoro-5-methylphenyl)urea (ABT-869), a 3-aminoindazole-based orally active multitargeted receptor tyrosine kinase inhibitor. , 2007, Journal of medicinal chemistry.
[61] G. Daley,et al. Mechanisms of Autoinhibition and STI-571/Imatinib Resistance Revealed by Mutagenesis of BCR-ABL , 2003, Cell.
[62] Donna Neuberg,et al. Characterization of AMN107, a selective inhibitor of native and mutant Bcr-Abl. , 2005, Cancer cell.
[63] Ling Wang,et al. AMG 706, an oral, multikinase inhibitor that selectively targets vascular endothelial growth factor, platelet-derived growth factor, and kit receptors, potently inhibits angiogenesis and induces regression in tumor xenografts. , 2006, Cancer research.
[64] Stover,et al. New anilinophthalazines as potent and orally well absorbed inhibitors of the VEGF receptor tyrosine kinases useful as antagonists of tumor-driven angiogenesis , 2000, Journal of medicinal chemistry.
[65] J. S. Johnson,et al. Discovery of heterocyclic ureas as a new class of raf kinase inhibitors: identification of a second generation lead by a combinatorial chemistry approach. , 2001, Bioorganic & medicinal chemistry letters.
[66] M. Zucchetti,et al. α1 Acid Glycoprotein Binds to Imatinib (STI571) and Substantially Alters Its Pharmacokinetics in Chronic Myeloid Leukemia Patients , 2003 .
[67] A. Doherty,et al. The discovery of the benzhydroxamate MEK inhibitors CI-1040 and PD 0325901. , 2008, Bioorganic & medicinal chemistry letters.
[68] Alan R. Saltiel,et al. Blockade of the MAP kinase pathway suppresses growth of colon tumors in vivo , 1999, Nature Medicine.
[69] Wei-Sheng Huang,et al. Discovery of 3-[2-(imidazo[1,2-b]pyridazin-3-yl)ethynyl]-4-methyl-N-{4-[(4-methylpiperazin-1-yl)methyl]-3-(trifluoromethyl)phenyl}benzamide (AP24534), a potent, orally active pan-inhibitor of breakpoint cluster region-abelson (BCR-ABL) kinase including the T315I gatekeeper mutant. , 2010, Journal of medicinal chemistry.
[70] A. Ullrich,et al. Strategies to overcome resistance to targeted protein kinase inhibitors , 2004, Nature Reviews Drug Discovery.
[71] S. Moro,et al. ATP non-competitive Ser/Thr kinase inhibitors as potential anticancer agents. , 2009, Anti-cancer agents in medicinal chemistry.
[72] Kevan M Shokat,et al. Features of selective kinase inhibitors. , 2005, Chemistry & biology.
[73] Taebo Sim,et al. A type-II kinase inhibitor capable of inhibiting the T315I "gatekeeper" mutant of Bcr-Abl. , 2010, Journal of medicinal chemistry.
[74] B. Druker,et al. Comparison of imatinib mesylate, dasatinib (BMS-354825), and nilotinib (AMN107) in an N-ethyl-N-nitrosourea (ENU)-based mutagenesis screen: high efficacy of drug combinations. , 2006, Blood.
[75] K. Kolaja,et al. Cardiotoxicity of kinase inhibitors: the prediction and translation of preclinical models to clinical outcomes , 2011, Nature Reviews Drug Discovery.
[76] Jürg Zimmermann,et al. Potent and selective inhibitors of the Abl-kinase: phenylamino-pyrimidine (PAP) derivatives , 1997 .
[77] D. Boschelli,et al. 2-Substituted aminopyrido[2,3-d]pyrimidin-7(8H)-ones. structure-activity relationships against selected tyrosine kinases and in vitro and in vivo anticancer activity. , 1998, Journal of medicinal chemistry.
[78] M. Vieth,et al. Kinomics: characterizing the therapeutically validated kinase space. , 2005, Drug discovery today.
[79] Xiao-Gao Liu,et al. Omega-carboxypyridyl substituted ureas as Raf kinase inhibitors: SAR of the amide substituent. , 2004, Bioorganic & medicinal chemistry letters.
[80] Stephen K Burley,et al. A Novel Mode of Gleevec Binding Is Revealed by the Structure of Spleen Tyrosine Kinase* , 2004, Journal of Biological Chemistry.
[81] Stanley J. Wiegand,et al. Vascular-specific growth factors and blood vessel formation , 2000, Nature.
[82] Rongshi Li,et al. Kinase Inhibitor Drugs , 2009 .
[83] C. Springer,et al. Small molecule inhibitors of BRAF in clinical trials. , 2012, Bioorganic & medicinal chemistry letters.
[84] R. Morphy. Selectively nonselective kinase inhibition: striking the right balance. , 2010, Journal of medicinal chemistry.
[85] Nathanael Gray,et al. Factors underlying sensitivity of cancers to small-molecule kinase inhibitors , 2009, Nature Reviews Drug Discovery.
[86] M. Stratton,et al. The cancer genome , 2009, Nature.
[87] Mindy I. Davis,et al. Comprehensive analysis of kinase inhibitor selectivity , 2011, Nature Biotechnology.
[88] S. Wilhelm,et al. Discovery and development of sorafenib: a multikinase inhibitor for treating cancer , 2006, Nature Reviews Drug Discovery.
[89] P. Savy,et al. Discovery of novel allosteric mitogen-activated protein kinase kinase (MEK) 1,2 inhibitors possessing bidentate Ser212 interactions. , 2012, Journal of medicinal chemistry.
[90] J. Boehm,et al. p38 MAP kinases: key signalling molecules as therapeutic targets for inflammatory diseases , 2003, Nature Reviews Drug Discovery.
[91] D. Auclair,et al. BAY 43-9006 Exhibits Broad Spectrum Oral Antitumor Activity and Targets the RAF/MEK/ERK Pathway and Receptor Tyrosine Kinases Involved in Tumor Progression and Angiogenesis , 2004, Cancer Research.
[92] Edward H. Kerns,et al. Drug-like Properties: Concepts, Structure Design and Methods: from ADME to Toxicity Optimization , 2008 .
[93] Samuel Singer,et al. PDGFRA Activating Mutations in Gastrointestinal Stromal Tumors , 2003, Science.
[94] Abran Q. Costales,et al. Design and synthesis of orally bioavailable benzimidazoles as Raf kinase inhibitors. , 2008, Journal of medicinal chemistry.
[95] J. Warmus,et al. Structures of human MAP kinase kinase 1 (MEK1) and MEK2 describe novel noncompetitive kinase inhibition , 2004, Nature Structural &Molecular Biology.
[96] Jeffrey Jie-Lou Liao,et al. Molecular recognition of protein kinase binding pockets for design of potent and selective kinase inhibitors. , 2007, Journal of medicinal chemistry.
[97] G. Daley,et al. 9-(Arenethenyl)purines as dual Src/Abl kinase inhibitors targeting the inactive conformation: design, synthesis, and biological evaluation. , 2009, Journal of medicinal chemistry.
[98] Nikolaus Stiefl,et al. Structural resemblances and comparisons of the relative pharmacological properties of imatinib and nilotinib. , 2010, Bioorganic & medicinal chemistry.
[99] Richard Kendall,et al. Evolution of a highly selective and potent 2-(pyridin-2-yl)-1,3,5-triazine Tie-2 kinase inhibitor. , 2007, Journal of medicinal chemistry.