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Volumn 51, Issue 19, 2008, Pages 6165-6172

2-Aminothienopyridazines as novel adenosine A1 receptor allosteric modulators and antagonists

Author keywords

[No Author keywords available]

Indexed keywords

5 AMINO 3 (4 TERT BUTYLPHENYL) 4 OXO 3,4 DIHYDROTHIENO[3,4 D]PYRIDAZINE 1 CARBOXYLATE; ADENOSINE A1 RECEPTOR ANTAGONIST; ETHYL 5 AMINO 3 (3 CHLOROPHENYL) 4 OXO 3,4 DIHYDROTHIENO[3,4 D]PYRIDAZINE 1 CARBOXYLATE; MITOGEN ACTIVATED PROTEIN KINASE 1; MITOGEN ACTIVATED PROTEIN KINASE 3; PYRIDAZINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 53549108359     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm800557d     Document Type: Article
Times cited : (49)

References (25)
  • 2
    • 0035209620 scopus 로고    scopus 로고
    • International Union of Pharmacology. XXV. Nomenclature and Classification of Adenosine Receptors
    • Fredholm, B. B.; IJzerman, A. P.; Jacobson, K. A.; Klotz, K.-N.; Linden, J. International Union of Pharmacology. XXV. Nomenclature and Classification of Adenosine Receptors. Pharmacol. Rev 2001, 53, 527-552.
    • (2001) Pharmacol. Rev , vol.53 , pp. 527-552
    • Fredholm, B.B.1    IJzerman, A.P.2    Jacobson, K.A.3    Klotz, K.-N.4    Linden, J.5
  • 3
    • 0038771191 scopus 로고    scopus 로고
    • Signalling from Adenosine Receptors to Mitogen-activated Protein Kinases
    • Schulte, G.; Fredholm, B. B. Signalling from Adenosine Receptors to Mitogen-activated Protein Kinases. Cell Signal. 2003, 15, 813-827.
    • (2003) Cell Signal , vol.15 , pp. 813-827
    • Schulte, G.1    Fredholm, B.B.2
  • 4
    • 33644770260 scopus 로고    scopus 로고
    • Adenosine Receptors as Therapeutic Targets
    • Jacobson, K. A.; Gao, Z.-G. Adenosine Receptors as Therapeutic Targets. Nat. Rev. Drug Disc. 2006, 5, 247-264.
    • (2006) Nat. Rev. Drug Disc , vol.5 , pp. 247-264
    • Jacobson, K.A.1    Gao, Z.-G.2
  • 6
    • 0025603686 scopus 로고
    • 1 Receptor Binding and Function by 2-Amino-3-benzoylthiophenes
    • 1 Receptor Binding and Function by 2-Amino-3-benzoylthiophenes. Mol. Pharmacol. 1990, 38, 939-949.
    • (1990) Mol. Pharmacol , vol.38 , pp. 939-949
    • Bruns, R.F.1    Fergus, J.H.2
  • 8
    • 0033539111 scopus 로고    scopus 로고
    • 1 Receptor. Synthesis and Biological Evaluation of Novel 2-Amino-3-benzoylthiophenes as Allosteric Enhancers of Agonist Binding
    • 1 Receptor. Synthesis and Biological Evaluation of Novel 2-Amino-3-benzoylthiophenes as Allosteric Enhancers of Agonist Binding. J. Med. Chem. 1999, 42, 3629-3635.
    • (1999) J. Med. Chem , vol.42 , pp. 3629-3635
    • van der Klein, P.A.M.1    Kourounakis, A.P.2    IJzerman, A.P.3
  • 12
    • 4644221135 scopus 로고    scopus 로고
    • Synthesis of 2-Amino-3-heteroaroylthiophenes and Evaluation of their Activity as Potential Allosteric Enhancers at the Human A 1 Receptor
    • Baraldi, P. G.; Pavani, M. G.; Shyrock, J. C.; Moorman, A. R.; Iannotta, V.; Borea, P. A.; Romagnoli, R. Synthesis of 2-Amino-3-heteroaroylthiophenes and Evaluation of their Activity as Potential Allosteric Enhancers at the Human A 1 Receptor. Eur. J. Med. Chem. 2004, 39, 855-865.
    • (2004) Eur. J. Med. Chem , vol.39 , pp. 855-865
    • Baraldi, P.G.1    Pavani, M.G.2    Shyrock, J.C.3    Moorman, A.R.4    Iannotta, V.5    Borea, P.A.6    Romagnoli, R.7
  • 13
    • 33747088125 scopus 로고    scopus 로고
    • 1 Adenosine Receptor Modulators Structurally Related to (2-Amino-4,5,6,7-tetrahydro-benzo[B]thiophen-3-yl)-(4-chloro-phenyl)methanone, a Potent Compound Useful to Reduce Neuropathic Pain. Med. Chem. Res. 2005, 14, 125-142.
    • 1 Adenosine Receptor Modulators Structurally Related to (2-Amino-4,5,6,7-tetrahydro-benzo[B]thiophen-3-yl)-(4-chloro-phenyl)methanone, a Potent Compound Useful to Reduce Neuropathic Pain. Med. Chem. Res. 2005, 14, 125-142.
  • 20
    • 76049086339 scopus 로고
    • Heterocycles from CH-acidic nitriles. VII. 2-Aminothiophene from α-Oxo Mercaptans and Methylene-active Nitriles
    • Gewald, K. Heterocycles from CH-acidic nitriles. VII. 2-Aminothiophene from α-Oxo Mercaptans and Methylene-active Nitriles. Chem. Ber. 1965, 98, 3571-3577.
    • (1965) Chem. Ber , vol.98 , pp. 3571-3577
    • Gewald, K.1
  • 21
    • 0009860642 scopus 로고    scopus 로고
    • Fast Synthesis of Aryl Triflates with Controlled Microwave Heating
    • Bengtson, A.; Hallberg, A.; Larhed, M. Fast Synthesis of Aryl Triflates with Controlled Microwave Heating. Org. Lett. 2002, 4, 1231-1233.
    • (2002) Org. Lett , vol.4 , pp. 1231-1233
    • Bengtson, A.1    Hallberg, A.2    Larhed, M.3
  • 22
    • 0346996805 scopus 로고    scopus 로고
    • 1 Adenosine Receptors Increase Receptor-G Protein Coupling and Counteract Guanine Nucleotide Effects on Agonist Binding
    • 1 Adenosine Receptors Increase Receptor-G Protein Coupling and Counteract Guanine Nucleotide Effects on Agonist Binding. Mol. Pharmacol. 2003, 64, 1557-1564.
    • (2003) Mol. Pharmacol , vol.64 , pp. 1557-1564
    • Figler, H.1    Olsson, R.A.2    Linden, J.3
  • 23
    • 26944466076 scopus 로고    scopus 로고
    • Osmond, R. I.; Sheehan, A.; Borowicz, R.; Barnett, E.; Harvey, G.; Turner, C.; Brown, A.; Crouch, M. F.; Dyer, A. R. GPCR Screening via ERK 1/2: A Novel Platform for Screening G Protein-Coupled Receptors. J. Biomol. Screening 2005, 10, 730-737.
    • Osmond, R. I.; Sheehan, A.; Borowicz, R.; Barnett, E.; Harvey, G.; Turner, C.; Brown, A.; Crouch, M. F.; Dyer, A. R. GPCR Screening via ERK 1/2: A Novel Platform for Screening G Protein-Coupled Receptors. J. Biomol. Screening 2005, 10, 730-737.
  • 25
    • 0345490945 scopus 로고    scopus 로고
    • International Union of Pharmacology Committee on Receptor Nomenclature and Drug Classification. XXXVIII. Update on Terms and Symbols in Quantitative Pharmacology
    • Neubig, R. R.; Spedding, M.; Kenakin, T. Christopoulos, A. International Union of Pharmacology Committee on Receptor Nomenclature and Drug Classification. XXXVIII. Update on Terms and Symbols in Quantitative Pharmacology. Pharmacol. Rev. 2003, 55, 597-606.
    • (2003) Pharmacol. Rev , vol.55 , pp. 597-606
    • Neubig, R.R.1    Spedding, M.2    Kenakin, T.3    Christopoulos, A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.