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Volumn 51, Issue 15, 2008, Pages 4449-4455

2-Amino-6-furan-2-yl-4-substituted nicotinonitriles as A2a adenosine receptor antagonists

Author keywords

[No Author keywords available]

Indexed keywords

2 [4 (2 CARBOXYETHYL)PHENETHYLAMINO]ADENOSINE 5' (N ETHYLCARBOXAMIDE); 2 AMINO 4 THIOPHEN 2 YL 6 FURAN 2 YL NICOTINONITRILE; 2 AMINO 4,6 DIFURAN 2 YL NICOTINONITRILE; 2 AMINO NICOTINONITRILE DERIVATIVE; ADENOSINE A1 RECEPTOR; ADENOSINE A2 RECEPTOR; ADENOSINE A3 RECEPTOR; ADENOSINE RECEPTOR A2A ANTAGONIST; ADENOSINE RECEPTOR BLOCKING AGENT; CYCLIC AMP; FURAN DERIVATIVE; LUF 6050; LUF 6080; PHENYL GROUP; UNCLASSIFIED DRUG;

EID: 49449100234     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm701594y     Document Type: Article
Times cited : (147)

References (31)
  • 3
    • 33644770260 scopus 로고    scopus 로고
    • Adenosine receptors as therapeutic targets
    • Jacobson, K. A.; Gao, Z.-G. Adenosine receptors as therapeutic targets. Nat. Rev. Drug Discovery 2006, 5, 247-264.
    • (2006) Nat. Rev. Drug Discovery , vol.5 , pp. 247-264
    • Jacobson, K.A.1    Gao, Z.-G.2
  • 4
    • 2442520220 scopus 로고    scopus 로고
    • 2A Adenosine Receptor Antagonists with 8-Styrylxanthine Structure: Potential Drug for Parkinson's Disease
    • 2A Adenosine Receptor Antagonists with 8-Styrylxanthine Structure: Potential Drug for Parkinson's Disease. J. Org. Chem. 2004, 69, 3308-3318.
    • (2004) J. Org. Chem , vol.69 , pp. 3308-3318
    • Hockemeyer, J.1    Burbiel, J.C.2    Müller, C.E.3
  • 7
    • 25144524190 scopus 로고    scopus 로고
    • 2A receptor antagonists. Bioorg. Med. Chem. Lett. 2005, 15, 4809-4813.
    • 2A receptor antagonists. Bioorg. Med. Chem. Lett. 2005, 15, 4809-4813.
  • 8
    • 22844440107 scopus 로고    scopus 로고
    • 2A antagonists. Part 1. Bioorg. Med. Chem. Lett. 2005, 15, 3670-3674.
    • 2A antagonists. Part 1. Bioorg. Med. Chem. Lett. 2005, 15, 3670-3674.
  • 9
    • 22844437672 scopus 로고    scopus 로고
    • 2A antagonists'. The successful reduction of hERG activity. Part 2. Bioorg. Med. Chem. Lett. 2005, 15, 3675-3678.
    • 2A antagonists'. The successful reduction of hERG activity. Part 2. Bioorg. Med. Chem. Lett. 2005, 15, 3675-3678.
  • 10
    • 19944432950 scopus 로고    scopus 로고
    • 2A adenosine receptor antagonists. Bioorg. Med. Chem. Lett. 2005, 15, 511-515.
    • 2A adenosine receptor antagonists. Bioorg. Med. Chem. Lett. 2005, 15, 511-515.
  • 18
    • 27444442267 scopus 로고    scopus 로고
    • 2A Adenosine Receptor Antagonists. Design, Synthesis, and Pharmacological Characterization. J. Med. Chem. 2005, 48, 6887-6896.
    • 2A Adenosine Receptor Antagonists. Design, Synthesis, and Pharmacological Characterization. J. Med. Chem. 2005, 48, 6887-6896.
  • 20
    • 33847063396 scopus 로고    scopus 로고
    • 2A antagonists. Bioorg. Med. Chem. Lett. 2007, 17, 1659-1662.
    • 2A antagonists. Bioorg. Med. Chem. Lett. 2007, 17, 1659-1662.
  • 21
    • 0842282173 scopus 로고    scopus 로고
    • Wavefunction Inc, Irvine, CA
    • Spartan '04; Wavefunction Inc.: Irvine, CA, 2005.
    • (2005) Spartan '04
  • 25
    • 84986534395 scopus 로고
    • A Simple Method for the Preparation of 2-Amino-4-Aryl-3-Cyanopyridines by the Condensation of Malononitrile with Aromatic Aldehydes and Alkyl Ketones in the Presence of Ammonium Acetate
    • Kambe, S.; Saito, K. A Simple Method for the Preparation of 2-Amino-4-Aryl-3-Cyanopyridines by the Condensation of Malononitrile with Aromatic Aldehydes and Alkyl Ketones in the Presence of Ammonium Acetate. Synthesis 1980, 6, 366-368.
    • (1980) Synthesis , vol.6 , pp. 366-368
    • Kambe, S.1    Saito, K.2
  • 27
    • 0015417053 scopus 로고
    • Utilization of Operational Schemes for Analog Synthesis in Drug Design
    • Topliss, J. G. Utilization of Operational Schemes for Analog Synthesis in Drug Design. J. Med. Chem. 1972, 15, 1006-1011.
    • (1972) J. Med. Chem , vol.15 , pp. 1006-1011
    • Topliss, J.G.1
  • 28
    • 49449088468 scopus 로고    scopus 로고
    • Anderson, D. R.; Stehle, N. W.; Kolodziej, S. A.; Reinhard, E. J. Preparation of aminocyanopyridines as inhibitors of mitogen activated protein kinase-activated protein kinase-2 for treating TNFα mediated diseases. WO 2004/055015 A1, 2004.
    • Anderson, D. R.; Stehle, N. W.; Kolodziej, S. A.; Reinhard, E. J. Preparation of aminocyanopyridines as inhibitors of mitogen activated protein kinase-activated protein kinase-2 for treating TNFα mediated diseases. WO 2004/055015 A1, 2004.
  • 29
    • 33646265008 scopus 로고    scopus 로고
    • The Molecule Evoluator. An interactive evolutionary algorithm for the design of drug-like molecules
    • Lameijer, E. W.; Kok, J. N.; Back, T; IJzerman, A. P. The Molecule Evoluator. An interactive evolutionary algorithm for the design of drug-like molecules. J. Chem. Inf. Model. 2006, 46, 545-552.
    • (2006) J. Chem. Inf. Model , vol.46 , pp. 545-552
    • Lameijer, E.W.1    Kok, J.N.2    Back, T.3    IJzerman, A.P.4
  • 30
    • 34247217238 scopus 로고    scopus 로고
    • Designing active template molecules by combining computational de novo design and human chemist's expertise
    • Lameijer, E. W.; Tromp, R. A.; Spanjersberg, R. F.; Brussee, J.; IJzerman, A. P. Designing active template molecules by combining computational de novo design and human chemist's expertise. J. Med. Chem. 2007, 50, 1925-1932.
    • (2007) J. Med. Chem , vol.50 , pp. 1925-1932
    • Lameijer, E.W.1    Tromp, R.A.2    Spanjersberg, R.F.3    Brussee, J.4    IJzerman, A.P.5
  • 31
    • 0031024171 scopus 로고    scopus 로고
    • Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
    • Lipinski, C. A.; Lombardo, F.; Dominy, B. W.; Feeney, P. J. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Adv. Drug Delivery Rev. 1997, 23, 3-25.
    • (1997) Adv. Drug Delivery Rev , vol.23 , pp. 3-25
    • Lipinski, C.A.1    Lombardo, F.2    Dominy, B.W.3    Feeney, P.J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.