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Volumn 14, Issue 5-6, 2009, Pages 291-297

Kinase-targeted libraries: The design and synthesis of novel, potent, and selective kinase inhibitors

Author keywords

[No Author keywords available]

Indexed keywords

CHECKPOINT KINASE 1; CYCLIN DEPENDENT KINASE 2; PHOSPHOTRANSFERASE INHIBITOR; PROTEIN KINASE INHIBITOR; PYRAZOLE; UNCLASSIFIED DRUG; VASCULOTROPIN RECEPTOR 2; VASCULOTROPIN RECEPTOR 2 INHIBITOR;

EID: 61649114657     PISSN: 13596446     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.drudis.2008.12.002     Document Type: Review
Times cited : (103)

References (20)
  • 1
    • 0036527429 scopus 로고    scopus 로고
    • Protein kinases - the major drug targets of the twenty-first century?
    • Cohen P. Protein kinases - the major drug targets of the twenty-first century?. Nat. Rev. Drug Discov. 1 (2002) 309-315
    • (2002) Nat. Rev. Drug Discov. , vol.1 , pp. 309-315
    • Cohen, P.1
  • 2
    • 20444436366 scopus 로고    scopus 로고
    • Drug discovery process for kinase inhibitors
    • Weinmann H., and Metternich R. Drug discovery process for kinase inhibitors. Chembiochem 6 (2005) 455-459
    • (2005) Chembiochem , vol.6 , pp. 455-459
    • Weinmann, H.1    Metternich, R.2
  • 3
    • 33846899405 scopus 로고    scopus 로고
    • Molecular recognition of protein kinase binding pockets for design of potent and selective kinase inhibitors
    • Liao J.J. Molecular recognition of protein kinase binding pockets for design of potent and selective kinase inhibitors. J. Med. Chem. 50 (2007) 409-424
    • (2007) J. Med. Chem. , vol.50 , pp. 409-424
    • Liao, J.J.1
  • 4
    • 24944497371 scopus 로고    scopus 로고
    • Features of selective kinase inhibitors
    • Knight Z.A., and Shokat K.M. Features of selective kinase inhibitors. Chem. Biol. 12 (2005) 621-637
    • (2005) Chem. Biol. , vol.12 , pp. 621-637
    • Knight, Z.A.1    Shokat, K.M.2
  • 5
    • 19944405127 scopus 로고    scopus 로고
    • Components of successful lead generation
    • Davis A.M., et al. Components of successful lead generation. Curr. Top. Med. Chem. 5 (2005) 421-439
    • (2005) Curr. Top. Med. Chem. , vol.5 , pp. 421-439
    • Davis, A.M.1
  • 6
    • 20444455036 scopus 로고    scopus 로고
    • Target-family-oriented focused libraries for kinases-conceptual design aspects and commercial availability
    • Prien O. Target-family-oriented focused libraries for kinases-conceptual design aspects and commercial availability. Chembiochem 6 (2005) 500-505
    • (2005) Chembiochem , vol.6 , pp. 500-505
    • Prien, O.1
  • 7
    • 34547817154 scopus 로고    scopus 로고
    • A new paradigm for protein kinase inhibition: blocking phosphorylation without directly targeting ATP binding
    • Bogoyevitch M.A., and Fairlie D.P. A new paradigm for protein kinase inhibition: blocking phosphorylation without directly targeting ATP binding. Drug. Discov. Today 12 (2007) 622-633
    • (2007) Drug. Discov. Today , vol.12 , pp. 622-633
    • Bogoyevitch, M.A.1    Fairlie, D.P.2
  • 8
    • 84871834562 scopus 로고    scopus 로고
    • The impact of protein kinase structures on drug discovery
    • Zhang C., and Kim S.-H. The impact of protein kinase structures on drug discovery. Comput. Struct. Appr. Drug Discov. 349 (2008) 349-365
    • (2008) Comput. Struct. Appr. Drug Discov. , vol.349 , pp. 349-365
    • Zhang, C.1    Kim, S.-H.2
  • 9
    • 33646586669 scopus 로고    scopus 로고
    • Preclinical activity of ABT-869, a multitargeted receptor tyrosine kinase inhibitor
    • Albert D.H., et al. Preclinical activity of ABT-869, a multitargeted receptor tyrosine kinase inhibitor. Mol. Cancer Ther. 5 (2006) 995-1006
    • (2006) Mol. Cancer Ther. , vol.5 , pp. 995-1006
    • Albert, D.H.1
  • 10
    • 20344384859 scopus 로고    scopus 로고
    • Potent and selective inhibitors of Akt kinases slow the progress of tumors in vivo
    • Luo Y., et al. Potent and selective inhibitors of Akt kinases slow the progress of tumors in vivo. Mol. Cancer Ther. 4 (2005) 977-986
    • (2005) Mol. Cancer Ther. , vol.4 , pp. 977-986
    • Luo, Y.1
  • 11
    • 34548118639 scopus 로고    scopus 로고
    • Design, synthesis, and biological activity of 5,10-dihydro-dibenzo[b,e][1,4]diazepin-11-one-based potent and selective Chk-1 inhibitors
    • Wang L., et al. Design, synthesis, and biological activity of 5,10-dihydro-dibenzo[b,e][1,4]diazepin-11-one-based potent and selective Chk-1 inhibitors. J. Med. Chem. 50 (2007) 4162-4176
    • (2007) J. Med. Chem. , vol.50 , pp. 4162-4176
    • Wang, L.1
  • 12
    • 17044403086 scopus 로고    scopus 로고
    • Ligand efficiency indices as guideposts for drug discovery
    • Abad-Zapatero C., and Metz J.T. Ligand efficiency indices as guideposts for drug discovery. Drug Discov. Today 10 (2005) 464-469
    • (2005) Drug Discov. Today , vol.10 , pp. 464-469
    • Abad-Zapatero, C.1    Metz, J.T.2
  • 13
    • 33845364148 scopus 로고    scopus 로고
    • Fragment-based drug design: how big is too big?
    • Hajduk P.J. Fragment-based drug design: how big is too big?. J. Med. Chem. 49 (2006) 6972-6976
    • (2006) J. Med. Chem. , vol.49 , pp. 6972-6976
    • Hajduk, P.J.1
  • 14
    • 42949088496 scopus 로고    scopus 로고
    • Chemical fragments as foundations for understanding target space and activity prediction
    • Sutherland J.J., et al. Chemical fragments as foundations for understanding target space and activity prediction. J. Med. Chem. 51 (2008) 2689-2700
    • (2008) J. Med. Chem. , vol.51 , pp. 2689-2700
    • Sutherland, J.J.1
  • 15
    • 0037463033 scopus 로고    scopus 로고
    • NMR spectroscopy techniques for screening and identifying ligand binding to protein receptors
    • Meyer B., and Peters T. NMR spectroscopy techniques for screening and identifying ligand binding to protein receptors. Angew Chem. Int. Ed. Engl. 42 (2003) 864-890
    • (2003) Angew Chem. Int. Ed. Engl. , vol.42 , pp. 864-890
    • Meyer, B.1    Peters, T.2
  • 16
    • 0033341062 scopus 로고    scopus 로고
    • NMR-based screening in drug discovery
    • Hajduk P.J., et al. NMR-based screening in drug discovery. Q Rev. Biophys. 32 (1999) 211-240
    • (1999) Q Rev. Biophys. , vol.32 , pp. 211-240
    • Hajduk, P.J.1
  • 17
    • 41849136167 scopus 로고    scopus 로고
    • Scaffold oriented synthesis. Part 2: design, synthesis and biological evaluation of pyrimido-diazepines as receptor tyrosine kinase inhibitors
    • Gracias V., et al. Scaffold oriented synthesis. Part 2: design, synthesis and biological evaluation of pyrimido-diazepines as receptor tyrosine kinase inhibitors. Bioorg. Med. Chem. Lett. 18 (2008) 2691-2695
    • (2008) Bioorg. Med. Chem. Lett. , vol.18 , pp. 2691-2695
    • Gracias, V.1
  • 18
    • 27744490073 scopus 로고    scopus 로고
    • Scaffold oriented synthesis. Part 1: design, preparation, and biological evaluation of thienopyrazoles as kinase inhibitors
    • Akritopoulou-Zanze I., et al. Scaffold oriented synthesis. Part 1: design, preparation, and biological evaluation of thienopyrazoles as kinase inhibitors. Bioorg. Med. Chem. Lett. 16 (2006) 96-99
    • (2006) Bioorg. Med. Chem. Lett. , vol.16 , pp. 96-99
    • Akritopoulou-Zanze, I.1
  • 19
    • 16244391116 scopus 로고    scopus 로고
    • Utilization of NMR-derived fragment leads in drug design
    • Huth J.R., et al. Utilization of NMR-derived fragment leads in drug design. Methods Enzymol. 394 (2005) 549-571
    • (2005) Methods Enzymol. , vol.394 , pp. 549-571
    • Huth, J.R.1
  • 20
    • 2942564021 scopus 로고    scopus 로고
    • Pursuing the leadlikeness concept in pharmaceutical research
    • Hann M.M., and Oprea T.I. Pursuing the leadlikeness concept in pharmaceutical research. Curr. Opin. Chem. Biol. 8 (2004) 255-263
    • (2004) Curr. Opin. Chem. Biol. , vol.8 , pp. 255-263
    • Hann, M.M.1    Oprea, T.I.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.