메뉴 건너뛰기




Volumn 84, Issue 1, 2012, Pages 21-29

Discovery of novel A 3 adenosine receptor ligands based on chromone scaffold

Author keywords

Adenosine receptor ligand; Chromone scaffold; Drug discovery

Indexed keywords

ADENOSINE A1 RECEPTOR; ADENOSINE A2A RECEPTOR; ADENOSINE A3 RECEPTOR; ADENOSINE RECEPTOR AFFECTING AGENT; CARBOXYLIC ACID DERIVATIVE; CHROMONE CARBOXAMIDE DERIVATIVE; CHROMONE DERIVATIVE; LIGAND; N (3,4 DIMETHOXYPHENYL) 4 OXO 4H 1 BENZOPYRAN 2 CARBOXAMIDE; N (4 METHOXYPHENYL) 4 OXO 4H 1 BENZOPYRAN 2; N (4 METHOXYPHENYL) 4 OXO 4H 1 BENZOPYRAN 2 CARBOXAMIDE; N (4 METHOXYPHENYL) 4 OXO 4H 1 BENZOPYRAN 3 CARBOXAMIDE; N (43, DIMETHOXYPHENYL) 4 OXO 4H 1 BENZOPYRAN 3 CARBOXAMIDE; UNCLASSIFIED DRUG; ADENOSINE A3 RECEPTOR ANTAGONIST;

EID: 84860664996     PISSN: 00062952     EISSN: 18732968     Source Type: Journal    
DOI: 10.1016/j.bcp.2012.03.007     Document Type: Article
Times cited : (43)

References (34)
  • 1
    • 12344252751 scopus 로고    scopus 로고
    • Mechanisms of cancer cell invasion
    • S. Erik Mechanisms of cancer cell invasion Curr Opin Genetics Dev 15 2005 87 96
    • (2005) Curr Opin Genetics Dev , vol.15 , pp. 87-96
    • Erik, S.1
  • 7
    • 51049101334 scopus 로고    scopus 로고
    • Adenosine receptors: Therapeutic aspects for inflammatory and immune diseases
    • G. Hasko, J. Linden, B. Cronstein, and P. Pacher Adenosine receptors: therapeutic aspects for inflammatory and immune diseases Nat Rev Drug Discov 7 2008 759 770
    • (2008) Nat Rev Drug Discov , vol.7 , pp. 759-770
    • Hasko, G.1    Linden, J.2    Cronstein, B.3    Pacher, P.4
  • 10
    • 38749132550 scopus 로고    scopus 로고
    • Adenosine receptor antagonists: Translating medicinal chemistry and pharmacology into clinical utility
    • P.G. Baraldi, M.A. Tabrizi, S. Gessi, and P.A. Borea Adenosine receptor antagonists: translating medicinal chemistry and pharmacology into clinical utility Chem Rev 108 2008 238 263
    • (2008) Chem Rev , vol.108 , pp. 238-263
    • Baraldi, P.G.1    Tabrizi, M.A.2    Gessi, S.3    Borea, P.A.4
  • 11
    • 84860663535 scopus 로고    scopus 로고
    • Introduction to adenosine receptors as therapeutic targets
    • C.N. Wilson, S.J. Mustafa, Springer-Verlag Berlin Heidelberg
    • K.A. Jacobson Introduction to adenosine receptors as therapeutic targets C.N. Wilson, S.J. Mustafa, Adenosine receptors in health and disease: 2009 Springer-Verlag Berlin Heidelberg
    • (2009) Adenosine Receptors in Health and Disease
    • Jacobson, K.A.1
  • 12
    • 79958211242 scopus 로고    scopus 로고
    • Drug discovery management, small is still beautiful: Why a number of companies get it wrong
    • J.S.K. Lars Drug discovery management, small is still beautiful: why a number of companies get it wrong Drug Discov Today 16 2011 476 484
    • (2011) Drug Discov Today , vol.16 , pp. 476-484
    • Lars, J.S.K.1
  • 14
    • 79960651250 scopus 로고    scopus 로고
    • Chromone, a privileged scaffold for the development of monoamine oxidase inhibitors
    • A. Gaspar, T. Silva, M. Yáñez, D. Vina, F. Orallo, and F. Ortuso Chromone, a privileged scaffold for the development of monoamine oxidase inhibitors J Med Chem 54 2011 5165 5173
    • (2011) J Med Chem , vol.54 , pp. 5165-5173
    • Gaspar, A.1    Silva, T.2    Yáñez, M.3    Vina, D.4    Orallo, F.5    Ortuso, F.6
  • 15
    • 79953066953 scopus 로고    scopus 로고
    • Towards the discovery of a novel class of monoamine oxidase inhibitors: Structure-property-activity and docking studies on chromone amides
    • A. Gaspar, F. Teixeira, E. Uriarte, N. Milhazes, A. Melo, and M.N.D.S. Cordeiro Towards the discovery of a novel class of monoamine oxidase inhibitors: structure-property-activity and docking studies on chromone amides ChemMedChem 6 2011 628 632
    • (2011) ChemMedChem , vol.6 , pp. 628-632
    • Gaspar, A.1    Teixeira, F.2    Uriarte, E.3    Milhazes, N.4    Melo, A.5    Cordeiro, M.N.D.S.6
  • 16
    • 0031931065 scopus 로고    scopus 로고
    • Comparative pharmacology of human adenosine receptor subtypes- characterization of stably transfected receptors in CHO cells
    • K.N. Klotz, J. Hessling, J. Hegler, C. Owman, B. Kull, and B.B. Fredholm Comparative pharmacology of human adenosine receptor subtypes-characterization of stably transfected receptors in CHO cells N-S Arch Pharmacol 357 1997 1 9
    • (1997) N-S Arch Pharmacol , vol.357 , pp. 1-9
    • Klotz, K.N.1    Hessling, J.2    Hegler, J.3    Owman, C.4    Kull, B.5    Fredholm, B.B.6
  • 19
    • 0020084268 scopus 로고
    • Validation, statistical analysis of a computer modeling method for quantitative analysis of radioligand binding data for mixtures of pharmacological receptor subtypes
    • A. De Lean, A.A. Hancock, and R.J. Lefkowitz Validation, statistical analysis of a computer modeling method for quantitative analysis of radioligand binding data for mixtures of pharmacological receptor subtypes J Mol Pharmacol 21 1982 5 16
    • (1982) J Mol Pharmacol , vol.21 , pp. 5-16
    • De Lean, A.1    Hancock, A.A.2    Lefkowitz, R.J.3
  • 20
    • 84860663534 scopus 로고    scopus 로고
    • MOE. (Molecular Operating Environment), version 2008.10; Chemical Computing Group Inc. (1010 Sherbrooke Street West, Suite 910, Montreal, Quebec, Canada H3A 2R7)
    • MOE. (Molecular Operating Environment), version 2008.10; software available from Chemical Computing Group Inc. (1010 Sherbrooke Street West, Suite 910, Montreal, Quebec, Canada H3A 2R7); http://www.chemcomp.com.
  • 23
    • 71749106590 scopus 로고    scopus 로고
    • 3 adenosine receptor as versatile G protein-coupled receptor example to validate the receptor homology modeling technology
    • 3 adenosine receptor as versatile G protein-coupled receptor example to validate the receptor homology modeling technology Curr Pharm Des 15 2009 4069 4084
    • (2009) Curr Pharm des , vol.15 , pp. 4069-4084
    • Morizzo, E.1    Federico, S.2    Spalluto, G.3    Human, M.S.4
  • 25
    • 77957055780 scopus 로고
    • Integrated methods for the construction of three-dimensional models and computational probing of structure-function relations in G protein-coupled receptors
    • C.S. Stuart, Academic Press
    • J.A. Ballesteros, and H. Weinstein Integrated methods for the construction of three-dimensional models and computational probing of structure-function relations in G protein-coupled receptors C.S. Stuart, Methods in neurosciences 1995 Academic Press 366 428
    • (1995) Methods in Neurosciences , pp. 366-428
    • Ballesteros, J.A.1    Weinstein, H.2
  • 26
    • 65249157397 scopus 로고    scopus 로고
    • Protonate 3D: Assignment of ionization states and hydrogen coordinates to macromolecular structures
    • P. Labute Protonate 3D: assignment of ionization states and hydrogen coordinates to macromolecular structures Proteins: Struct Funct Bioinf 75 2009 187 205
    • (2009) Proteins: Struct Funct Bioinf , vol.75 , pp. 187-205
    • Labute, P.1
  • 27
    • 84860688895 scopus 로고    scopus 로고
    • GOLD suite, version 4.0.1; Cambridge Crystallographic Data Centre Cambridge Crystallographic Data Centre (12 Union Road Cambridge CB2 1EZ UK)
    • GOLD suite, version 4.0.1; software available from Cambridge Crystallographic Data Centre Cambridge Crystallographic Data Centre (12 Union Road Cambridge CB2 1EZ UK); http://www.ccdc.cam.ac.uk.
  • 28
    • 12144289984 scopus 로고    scopus 로고
    • Glide: A new approach for rapid, accurate docking and scoring. 1. Method and assessment of docking accuracy
    • R.A. Friesner, J.L. Banks, R.B. Murphy, T.A. Halgren, J.J. Klicic, and D.T. Mainz Glide: A new approach for rapid, accurate docking and scoring. 1. Method and assessment of docking accuracy J Med Chem 47 2004 1739 1749
    • (2004) J Med Chem , vol.47 , pp. 1739-1749
    • Friesner, R.A.1    Banks, J.L.2    Murphy, R.B.3    Halgren, T.A.4    Klicic, J.J.5    Mainz, D.T.6
  • 29
    • 62449330667 scopus 로고    scopus 로고
    • Empirical scoring functions for advanced protein-ligand docking with PLANTS
    • O. Korb, T. Stutzle, and T.E. Exner Empirical scoring functions for advanced protein-ligand docking with PLANTS J Chem Inf Model 49 2009 84 96
    • (2009) J Chem Inf Model , vol.49 , pp. 84-96
    • Korb, O.1    Stutzle, T.2    Exner, T.E.3
  • 30
    • 79959403001 scopus 로고    scopus 로고
    • Metal-catalysed approaches to amide bond formation
    • C.L. Allen, and J.M.J. Williams Metal-catalysed approaches to amide bond formation Chem Soc Rev 40 2011 3405 3415
    • (2011) Chem Soc Rev , vol.40 , pp. 3405-3415
    • Allen, C.L.1    Williams, J.M.J.2
  • 31
    • 1342302805 scopus 로고    scopus 로고
    • Recent development of peptide coupling reagents in organic synthesis
    • S.-Y. Han, and Y.-A. Kim Recent development of peptide coupling reagents in organic synthesis Tetrahedron 60 2004 2447 2467
    • (2004) Tetrahedron , vol.60 , pp. 2447-2467
    • Han, S.-Y.1    Kim, Y.-A.2
  • 32
    • 0011784322 scopus 로고    scopus 로고
    • General methods of preparing chromones
    • John Wiley & Sons, Inc.
    • G.P. Ellis General methods of preparing chromones Chemistry of heterocyclic compounds 2008 John Wiley & Sons, Inc. pp. 495-555
    • (2008) Chemistry of Heterocyclic Compounds , pp. 495-555
    • Ellis, G.P.1
  • 33
    • 0029043501 scopus 로고
    • Site-directed mutagenesis identifies residues involved in ligand recognition in the human A adenosine receptor
    • J. Kim, J. Wess, A.M. van Rhee, T. Schöneberg, and K.A. Jacobson Site-directed mutagenesis identifies residues involved in ligand recognition in the human A adenosine receptor J Biol Chem 270 1995 13987 13997
    • (1995) J Biol Chem , vol.270 , pp. 13987-13997
    • Kim, J.1    Wess, J.2    Van Rhee, A.M.3    Schöneberg, T.4    Jacobson, K.A.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.