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Volumn 193, Issue , 2009, Pages 99-122

Recent developments in A2B adenosine receptor ligands

Author keywords

Adenosine receptor antagonist; Asthma; CVT 6883; LAS 38096; MRE2029F20

Indexed keywords

1 BUTYL 8 (4 CARBOXYPHENYL)XANTHINE; 1 PROPYL 8 (4 SULFOPHENYL)XANTHINE; 2 (3 FLUOROPYRIDIN 4 YL) 3,6 DI(3 PYRIDYL) 5H PYRROLO[2,3 B]PYRAZINE; 2 (3,4 DIMETHOXYPHENYL) N [5 (2,6 DIOXO 1,3 DIPROPYL 2,3,6,7 TETRAHYDRO 1H PURIN 8 YL) 1 METHYL 1H PYRAZOL 3 YL]ACETAMIDE; 2 [4 (2 CARBOXYETHYL)PHENETHYLAMINO]ADENOSINE 5' (N ETHYLCARBOXAMIDE); 2 AMINO 6 (2 FURYL) 3 METHYL 5 (4 PYRIDYL)PYRIMIDIN 4(3H) ONE; 4 (1,3 DIALKYL 2,4 DIOXO 2,3,4,5 TETRAHYDRO 1H PYRROLO[3,2 D]PYRIMIDIN 6 YL)BENZENESULFONAMIDE DERIVATIVE; 6 AMINO 2 (2 FURYL) 3,4' BIPYRIDINE 5 CARBONITRILE; 8 (4 CARBOXYMETHOXYPHENYL) 1,3 DIPROPYLXANTHINE; 8 (4 PYRAZOLYL)XANTHINE DERIVATIVE; 8 (5 PYRAZOLYL)XANTHINE; 8 CYCLOPENTYL 1,3 DIPROPYLXANTHINE; 8 PHENYLTHEOPHYLLINE; ADENOSINE A2 RECEPTOR ANTAGONIST; ADENOSINE A2B RECEPTOR; ADENOSINE A2B RECEPTOR ANTAGONIST; AMINOPYRIMIDINE DERIVATIVE; CAFFEINE; CVT 6883; DIMETHYLMALAMIDE DERIVATIVE; IMIDAZOPYRIDINE DERIVATIVE; LAS 38096; MRE 2028F20; MRE 2029F20; MRE 2030F20; MRS 1595; MRS 1706; N (3,4 DIMETHOXYPHENYL) 2 [5 (2,6 DIOXO 1,3 DIPROPYL 2,3,6,7 TETRAHYDRO 1H PURIN 8 YL) 1 METHYL 1H PYRAZOL 3 YLOXY]ACETAMIDE; N (4 BROMOPHENYL) 2 [4 (1,3 DIMETHYL 2,4 DIOXO 2,3,4,5 TETRAHYDRO 1H PYRROLO[3,2 D]PYRIMIDIN 6 YL)PHENOXY]ACETAMIDE; N (4 CYANOPHENYL) 2 [4 (2,3,6,7 TETRAHYDRO 2,6 DIOXO 1,3 DIPROPYL 1H PURIN 8 YL)PHENOXY]ACETAMIDE; N BENZO[1,3]DIOXOL 5 YL 2 [5 (2,6 DIOXO 1,3 DIPROPYL 2,3,6,7 TETRAHYDRO 1H PURIN 8 YL) 1 METHYL 1H PYRAZOL 3 YLOXY]ACETAMIDE; OSIP 339391; PSB 1115; PYRAZOLO[4,3 E] 1,2,4 TRIAZOLO [1,5 C]PYRIMIDINE DERIVATIVE; PYRIMIDINE 2 (AMINO 5 PYRIMIDINYL)PYRIMIDINE; THEOPHYLLINE; UNCLASSIFIED DRUG; UNINDEXED DRUG; ADENINE; AMINOPYRIDINE DERIVATIVE; PYRAZINE DERIVATIVE; PYRIMIDINE DERIVATIVE; XANTHINE DERIVATIVE;

EID: 70349306890     PISSN: 01712004     EISSN: None     Source Type: Book Series    
DOI: 10.1007/978-3-540-89615-9_4     Document Type: Review
Times cited : (32)

References (53)
  • 3
    • 84930215128 scopus 로고    scopus 로고
    • A potent adenosine A2B receptor antagonist attenuates methacholine-induced bronchial hyperresponsiveness, mucus production and IgE levels in an allergic mouse model (Poster 162
    • 5-10 May 2006
    • Aparici M, Nueda A, Beleta J, Prats N, Fernandez R, Miralpeix M (2006) A potent adenosine A2B receptor antagonist attenuates methacholine-induced bronchial hyperresponsiveness, mucus production and IgE levels in an allergic mouse model (Poster 162). In: CIA Symp, Malta, 5-10 May 2006
    • (2006) CIA Symp, Malta
    • Aparici, M.1    Nueda, A.2    Beleta, J.3    Prats, N.4    Fernandez, R.5    Miralpeix, M.6
  • 5
    • 0035028962 scopus 로고    scopus 로고
    • Pyrazolo[4,3-e] 1 1,2,4-triazolo[1,5-c]pyrimidine derivatives: A new pharmacological tool for the characterization of the human A3 adenosine receptor
    • Baraldi PG, Cacciari B, Romagnoli R, Spalluto G, Varani K, Gessi S, Merighi S, Borea PA (2001) Pyrazolo[4,3-e]1,2,4-triazolo[1,5-c]pyrimidine derivatives: a new pharmacological tool for the characterization of the human A3 adenosine receptor. Drug Dev Res 52:406-415
    • (2001) Drug Dev Res , vol.52 , pp. 406-415
    • Baraldi, P.G.1    Cacciari, B.2    Romagnoli, R.3    Spalluto, G.4    Varani, K.5    Gessi, S.6    Merighi, S.7    Borea, P.A.8
  • 13
    • 0021350144 scopus 로고
    • Adenosine-induced bronchoconstriction in asthma: Antagonism by inhaled theophylline
    • Cushley MJ, Tattersfield AE, Holgate ST (1984) Adenosine-induced bronchoconstriction in asthma: antagonism by inhaled theophylline. Am Rev Respir Dis 129:380-384
    • (1984) Am Rev Respir Dis , vol.129 , pp. 380-384
    • Cushley, M.J.1    Tattersfield, A.E.2    Holgate, S.T.3
  • 16
    • 41849149631 scopus 로고    scopus 로고
    • Discovery of a novel A2B adenosine receptor antagonist as a clinical candidate for chronic inflammatory airway diseases
    • Elzein E, Kalla RV, Li X, Perry T, Gimbel A, Zeng D, Lustig D, Leung K, Zablocki J (2008) Discovery of a novel A2B adenosine receptor antagonist as a clinical candidate for chronic inflammatory airway diseases. J Med Chem 51:2267-2278
    • (2008) J Med Chem , vol.51 , pp. 2267-2278
    • Elzein, E.1    Kalla, R.V.2    Li, X.3    Perry, T.4    Gimbel, A.5    Zeng, D.6    Lustig, D.7    Leung, K.8    Zablocki, J.9
  • 18
    • 0032452871 scopus 로고    scopus 로고
    • Adenosine A2B receptors as therapeutic targets
    • Feoktistov I, Wells JN, Biaggioni I (1998) Adenosine A2B receptors as therapeutic targets. Drug Dev Res 45:198-206
    • (1998) Drug Dev Res , vol.45 , pp. 198-206
    • Feoktistov, I.1    Wells, J.N.2    Biaggioni, I.3
  • 19
    • 7244234161 scopus 로고    scopus 로고
    • Hypoxia modulates adenosine receptors in human endothelial and smooth muscle cells toward an A2B angiogenic phenotype
    • Feoktistov I, Ryzhov S, Zhong H, Goldstein AE, Matafonov A, Zeng D, Biaggioni I (2004) Hypoxia modulates adenosine receptors in human endothelial and smooth muscle cells toward an A2B angiogenic phenotype. Hypertension 44:649-654
    • (2004) Hypertension , vol.44 , pp. 649-654
    • Feoktistov, I.1    Ryzhov, S.2    Zhong, H.3    Goldstein, A.E.4    Matafonov, A.5    Zeng, D.6    Biaggioni, I.7
  • 20
    • 0035985601 scopus 로고    scopus 로고
    • Adenosine receptor ligands as potential therapeutics in asthma
    • Fozard JR, McCarth C (2002) Adenosine receptor ligands as potential therapeutics in asthma. Curr Opin Investig Drugs 3:69-77
    • (2002) Curr Opin Investig Drugs , vol.3 , pp. 69-77
    • Fozard, J.R.1    McCarth, C.2
  • 21
    • 0035209620 scopus 로고    scopus 로고
    • International Union of Pharmacology. XXV. Nomenclature and classification of adenosine receptors
    • Fredholm BB, IJzerman AP, Jacobson KA, Kloz K-N, Linden J (2001) International Union of Pharmacology. XXV. Nomenclature and classification of adenosine receptors. Pharmacol Rev 53:527-552
    • (2001) Pharmacol Rev , vol.53 , pp. 527-552
    • Fredholm, B.B.1    Ijzerman, A.P.2    Jacobson, K.A.3    Kloz, K.-N.4    Linden, J.5
  • 27
    • 30444441037 scopus 로고    scopus 로고
    • The Quintiles Prize Lecture 2004: The identification of the adenosine A2B receptor as a novel therapeutic target in asthma
    • Holgate ST (2005) The Quintiles Prize Lecture 2004: the identification of the adenosine A2B receptor as a novel therapeutic target in asthma. Br J Pharmacol 145:1009-1015
    • (2005) Br J Pharmacol , vol.145 , pp. 1009-1015
    • Holgate, S.T.1
  • 28
    • 0033014225 scopus 로고    scopus 로고
    • 1,3-Dialkylxanthie derivatives having high potency as antagonists at human A2B adenosine receptors
    • Jacobson KA, IJzerman AP, Linden J (1999) 1,3-Dialkylxanthie derivatives having high potency as antagonists at human A2B adenosine receptors. Drug Dev Res 47:45-53
    • (1999) Drug Dev Res , vol.47 , pp. 45-53
    • Jacobson, K.A.1    Ijzerman, A.P.2    Linden, J.3
  • 32
    • 38949111028 scopus 로고    scopus 로고
    • Selective, high affinity A2B adenosine receptor antagonists: N-1 monosubstituted 8-(pyrazol-4-yl)xanthines
    • Kalla R, Elzein E, Perry T, Li X, Gimbel A, Yang M, Zeng D, Zablocki J (2008) Selective, high affinity A2B adenosine receptor antagonists: N-1 monosubstituted 8-(pyrazol-4-yl)xanthines. Bioorg Med Chem Lett 18:1397-1401
    • (2008) Bioorg Med Chem Lett , vol.18 , pp. 1397-1401
    • Kalla, R.1    Elzein, E.2    Perry, T.3    Li, X.4    Gimbel, A.5    Yang, M.6    Zeng, D.7    Zablocki, J.8
  • 33
    • 0032871686 scopus 로고    scopus 로고
    • Acyl hydrazide derivatives of a xanthine carboxylic congener (XCC) as selective antagonists at human A2B adenosine receptor
    • Kim Y-C, Karton Y, Ji X-D, Melman N, Linden J, Jacobson KA (1999) Acyl hydrazide derivatives of a xanthine carboxylic congener (XCC) as selective antagonists at human A2B adenosine receptor. Drug Dev Res 47:178-188
    • (1999) Drug Dev Res , vol.47 , pp. 178-188
    • Kim, Y.-C.1    Karton, Y.2    Ji, X.-D.3    Melman, N.4    Linden, J.5    Jacobson, K.A.6
  • 34
    • 0034704901 scopus 로고    scopus 로고
    • Anilide derivatives of a 8-phenylxanthine carboxylic congener are highly potent and selective antagonists at human A2B adenosine receptors
    • Kim Y-C, Ji X-D, Melman N, Linden J, Jacobson KA (2000) Anilide derivatives of a 8-phenylxanthine carboxylic congener are highly potent and selective antagonists at human A2B adenosine receptors. J Med Chem 43:1165-1172
    • (2000) J Med Chem , vol.43 , pp. 1165-1172
    • Kim, Y.-C.1    Ji, X.-D.2    Melman, N.3    Linden, J.4    Jacobson, K.A.5
  • 35
    • 0037161610 scopus 로고    scopus 로고
    • Structure-activity relationships at human and rat A2B adenosine receptors of xanthine derivatives substituted at the 1-, 3-, 7-, and 8-positions
    • Kim S-A, Marshall MA, Melman N, Kim HS, M̈uller CE, Linden J, Jacobson KA (2002) Structure-activity relationships at human and rat A2B adenosine receptors of xanthine derivatives substituted at the 1-, 3-, 7-, and 8-positions. J Med Chem 45:2131-2138
    • (2002) J Med Chem , vol.45 , pp. 2131-2138
    • Kim, S.-A.1    Marshall, M.A.2    Melman, N.3    Kim, H.S.4    M̈uller, C.E.5    Linden, J.6    Jacobson, K.A.7
  • 38
    • 33847159974 scopus 로고    scopus 로고
    • Effect of a specific and selective A2B adenosine receptor antagonist on adenosine agonist AMP and allergen-induced airway responsiveness and cellular influx in a mouse model of asthma
    • Mustafa SJ, Nadeem A, Fan M, Zhong H, Belardinelli, Zeng D (2007) Effect of a specific and selective A2B adenosine receptor antagonist on adenosine agonist AMP and allergen-induced airway responsiveness and cellular influx in a mouse model of asthma. J Pharmacol Exp Ther 320:1246-1251
    • (2007) J Pharmacol Exp Ther , vol.320 , pp. 1246-1251
    • Mustafa, S.J.1    Nadeem, A.2    Fan, M.3    Zhong, H.4    Belardinelli Zeng, D.5
  • 39
    • 0141457802 scopus 로고    scopus 로고
    • Pyrazolo[4,3-e]-1, 2,4-triazolo[1,5-c]pyrimidine derivatives as adenosine receptor antagonists. Influence of the N5 substituent on the affinity at the human A3 and A2B adenosine receptor subtypes: A molecular modelling investigation
    • Pastorin G, Da Ros T, Spalluto G, Deflorian F, Moro S, Cacciari B, Baraldi PG, Gessi S, Varani K, Borea PA (2003) Pyrazolo[4,3-e]-1,2,4-triazolo[1, 5-c]pyrimidine derivatives as adenosine receptor antagonists. Influence of the N5 substituent on the affinity at the human A3 and A2B adenosine receptor subtypes: a molecular modelling investigation. J Med Chem 46:4287-4296
    • (2003) J Med Chem 46 , pp. 4287-4296
    • Pastorin, G.1    Da Ros, T.2    Spalluto, G.3    Deflorian, F.4    Moro, S.5    Cacciari, B.6    Baraldi, P.G.7    Gessi, S.8    Varani, K.9    Borea, P.A.10
  • 40
    • 54849413546 scopus 로고    scopus 로고
    • 1,3-Dialkyl-8-(hetero)aryl-9-OH-9-deazaxanthines as potent A2B adenosine receptor antagonists: Design, synthesis, structure-affinity and structure-selectivity relationships
    • Stefanachi A, Nicolotti O, Leonetti F, Cellamare S, Campagna F, Loza MI, Brea JM, Mazza F, Gavuzzo E and Carotti A (2008) 1,3-Dialkyl-8-(hetero)aryl-9- OH-9-deazaxanthines as potent A2B adenosine receptor antagonists: design, synthesis, structure-affinity and structure-selectivity relationships. Bioorg Med Chem 16:9780-9789
    • (2008) Bioorg Med Chem , vol.16 , pp. 9780-9789
    • Stefanachi, A.1    Nicolotti, O.2    Leonetti, F.3    Cellamare, S.4    Campagna, F.5    Loza, M.I.6    Brea, J.M.7    Mazza, F.8    Gavuzzo, E.9    Carotti, A.10
  • 49
    • 0842282741 scopus 로고    scopus 로고
    • Preparation, properties, reactions, and adenosine receptor affinities of sulfophenylxanthine nitrophenyl esters: Toward the development of sulfonic acid prodrugs with peroral bioavailability
    • Yan L, M̈uller CE (2004) Preparation, properties, reactions, and adenosine receptor affinities of sulfophenylxanthine nitrophenyl esters: toward the development of sulfonic acid prodrugs with peroral bioavailability. J Med Chem 47:10311043
    • (2004) J Med Chem , vol.47 , pp. 10311043
    • Yan, L.1    M̈uller, C.E.2
  • 52
    • 11144230939 scopus 로고    scopus 로고
    • Synergy between A2B adenosine receptors andhypoxia in activating human lung fibroblasts
    • Zhong H, Belardinelli L, Maa T, Zeng D (2005) Synergy between A2B adenosine receptors andhypoxia in activating human lung fibroblasts. Am J Respir Cell Mol Biol 32:2-8
    • (2005) Am J Respir Cell Mol Biol , vol.32 , pp. 2-8
    • Zhong, H.1    Belardinelli, L.2    Maa, T.3    Zeng, D.4
  • 53
    • 33750687938 scopus 로고    scopus 로고
    • A2B adenosine receptors induce IL-19 from bronchial epithelial cells and results in TNF-alpha increase
    • Zhong H, Wu Y, Belardinelli L, Zeng D (2006) A2B adenosine receptors induce IL-19 from bronchial epithelial cells and results in TNF-alpha increase. Am J Respir Cell Mol Biol 35:587-592
    • (2006) Am J Respir Cell Mol Biol , vol.35 , pp. 587-592
    • Zhong, H.1    Wu, Y.2    Belardinelli, L.3    Zeng, D.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.