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Volumn 50, Issue 4, 2007, Pages 828-834

2,6,8-Trisubstituted 1-deazapurines as adenosine receptor antagonists

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE A1 RECEPTOR; ADENOSINE RECEPTOR BLOCKING AGENT; FORSKOLIN; IMIDAZO[4,5 B]PYRIDINE DERIVATIVE; LUF 5816; LUF 5978; LUF 5980; LUF 5981; LUF 5983; UNCLASSIFIED DRUG;

EID: 33847366159     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm0607956     Document Type: Article
Times cited : (37)

References (18)
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    • Deazapurine Derivatives. X. Synthesis and Reactions of 5,7-Disubstituted Imidazo[4,5-b]pyridines
    • Schelling, J. E.; Salemink, C. A. Deazapurine Derivatives. X. Synthesis and Reactions of 5,7-Disubstituted Imidazo[4,5-b]pyridines. Rec. Trav. Chim. Pays-Bas 1972, 91, 650-656.
    • (1972) Rec. Trav. Chim. Pays-Bas , vol.91 , pp. 650-656
    • Schelling, J.E.1    Salemink, C.A.2
  • 7
    • 0019167326 scopus 로고
    • Synthesis of Imidazo[4,5-b]- and [4,5-c]pyridines
    • Middleton, R. W.; Wibberley, D. G. Synthesis of Imidazo[4,5-b]- and [4,5-c]pyridines. J. Heterocycl. Chem. 1980, 17, 1757-1760.
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    • Middleton, R.W.1    Wibberley, D.G.2
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    • Polyfunctional Pyridines from Nitroacetamidine and β-Diketones. A Useful Synthesis of Substituted Imidazo[4,5-b]pyridines and Related Compounds
    • Batt, D. G.; Houghton, G. C. Polyfunctional Pyridines from Nitroacetamidine and β-Diketones. A Useful Synthesis of Substituted Imidazo[4,5-b]pyridines and Related Compounds. J. Heterocycl. Chem. 1995, 32, 963-969.
    • (1995) J. Heterocycl. Chem , vol.32 , pp. 963-969
    • Batt, D.G.1    Houghton, G.C.2
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    • 1342281242 scopus 로고    scopus 로고
    • Simple and Efficient Method for the Preparation of Symmetrical Carboxylic Acid Anhydrides
    • Kazemi, F.; Sharghi, H.; Ali Nasseri, M. A Cheap, Simple and Efficient Method for the Preparation of Symmetrical Carboxylic Acid Anhydrides. Synthesis 2004, 2, 205-207.
    • (2004) Synthesis , vol.2 , pp. 205-207
    • Kazemi, F.1    Sharghi, H.2    Ali Nasseri, M.3    Cheap, A.4
  • 13
    • 3142543178 scopus 로고    scopus 로고
    • New, Non-Adenosine, High-Potency Agonists for the Human Adenosine A2B Receptor with an Improved Selectivity Profile Compared to the Reference Agonist N-Ethylcarboxamidoadenosine
    • Beukers, M. W.; Chang, L. C. W.; von Frijtag Drabbe Künzel, J.; Mulder-Krieger, T.; Spanjersberg, R. F.; Brussee, J.; IJzerman, A. P. New, Non-Adenosine, High-Potency Agonists for the Human Adenosine A2B Receptor with an Improved Selectivity Profile Compared to the Reference Agonist N-Ethylcarboxamidoadenosine. J. Med. Chem. 2004, 47, 3707-3709.
    • (2004) J. Med. Chem , vol.47 , pp. 3707-3709
    • Beukers, M.W.1    Chang, L.C.W.2    von Frijtag Drabbe Künzel, J.3    Mulder-Krieger, T.4    Spanjersberg, R.F.5    Brussee, J.6    IJzerman, A.P.7
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    • Potential Purine Antagonists. 7. Synthesis of 3-β-D-Ribofuranosyl-7-Aminoimidazo(4,5-b)Pyridine (1-Deazaadenosine)
    • Jain, P. C.; Chatterjee, S. K.; Anand, N. Potential Purine Antagonists. 7. Synthesis of 3-β-D-Ribofuranosyl-7-Aminoimidazo(4,5-b)Pyridine (1-Deazaadenosine). Indian J. Chem. 1966, 4, 403-405.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.