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Volumn 55, Issue 7, 2012, Pages 3563-3567

Novel 3,6,7-substituted pyrazolopyrimidines as positive allosteric modulators for the hydroxycarboxylic acid receptor 2 (GPR109A)

Author keywords

[No Author keywords available]

Indexed keywords

3 (4 ISOPROPYLPHENYL) 7 METHYL N ( PHENOXYETHYL)PYRAZOLO[1,5 A]PYRIMIDIN 6 CARBOXAMIDE; 3 HYDROXYBUTYRIC ACID; G PROTEIN COUPLED RECEPTOR; G PROTEIN COUPLED RECEPTOR 109 A; NICOTINIC ACID; PYRAZOLOPYRIMIDINE DERIVATIVE; PYRIMIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 84859789565     PISSN: 00222623     EISSN: 15204804     Source Type: Journal    
DOI: 10.1021/jm300164q     Document Type: Article
Times cited : (15)

References (20)
  • 1
    • 79955769365 scopus 로고    scopus 로고
    • International Union of Basic and Clinical Pharmacology. LXXXII: Nomenclature and classification of hydroxy-carboxylic acid receptors (GPR81, GPR109A, and GPR109B)
    • Offermanns, S.; Colletti, S. L.; Lovenberg, T. W.; Semple, G.; Wise, A.; IJzerman, A. P. International Union of Basic and Clinical Pharmacology. LXXXII: Nomenclature and classification of hydroxy-carboxylic acid receptors (GPR81, GPR109A, and GPR109B) Pharmacol. Rev. 2011, 63, 269-290
    • (2011) Pharmacol. Rev. , vol.63 , pp. 269-290
    • Offermanns, S.1    Colletti, S.L.2    Lovenberg, T.W.3    Semple, G.4    Wise, A.5    Ijzerman, A.P.6
  • 2
    • 0035666867 scopus 로고    scopus 로고
    • PUMA-G, an IFN-gamma-inducible gene in macrophages is a novel member of the seven transmembrane spanning receptor superfamily
    • Schaub, A.; Futterer, A.; Pfeffer, K. PUMA-G, an IFN-gamma-inducible gene in macrophages is a novel member of the seven transmembrane spanning receptor superfamily Eur. J. Immunol. 2001, 31, 3714-3725
    • (2001) Eur. J. Immunol. , vol.31 , pp. 3714-3725
    • Schaub, A.1    Futterer, A.2    Pfeffer, K.3
  • 3
    • 0037352280 scopus 로고    scopus 로고
    • PUMA-G and HM74 are receptors for nicotinic acid and mediate its anti-lipolytic effect
    • Tunaru, S.; Kero, J.; Schaub, A.; Wufka, C.; Blaukat, A.; Pfeffer, K.; Offermanns, S. PUMA-G and HM74 are receptors for nicotinic acid and mediate its anti-lipolytic effect Nat. Med. 2003, 9, 352-355
    • (2003) Nat. Med. , vol.9 , pp. 352-355
    • Tunaru, S.1    Kero, J.2    Schaub, A.3    Wufka, C.4    Blaukat, A.5    Pfeffer, K.6    Offermanns, S.7
  • 6
    • 27544491916 scopus 로고    scopus 로고
    • Characterization of determinants of ligand binding to the nicotinic acid receptor GPR109A (HM74A/PUMA-G)
    • Tunaru, S.; Lattig, J.; Kero, J.; Krause, G.; Offermanns, S. Characterization of determinants of ligand binding to the nicotinic acid receptor GPR109A (HM74A/PUMA-G) Mol. Pharmacol. 2005, 68, 1271-1280
    • (2005) Mol. Pharmacol. , vol.68 , pp. 1271-1280
    • Tunaru, S.1    Lattig, J.2    Kero, J.3    Krause, G.4    Offermanns, S.5
  • 9
    • 77957806526 scopus 로고    scopus 로고
    • High-affinity niacin GPR109A receptor agonists
    • Shen, H. C.; Colletti, S. L. High-affinity niacin GPR109A receptor agonists Annu. Rep. Med. Chem. 2010, 45, 73-94
    • (2010) Annu. Rep. Med. Chem. , vol.45 , pp. 73-94
    • Shen, H.C.1    Colletti, S.L.2
  • 10
    • 51349100188 scopus 로고    scopus 로고
    • Discovery of pyrazolopyrimidines as the first class of allosteric agonists for the high affinity nicotinic acid receptor GPR109A
    • Shen, H. C.; Taggart, A. K. P.; Wilsie, L. C.; Waters, M. G.; Hammond, M. L.; Tata, J. R.; Colletti, S. L. Discovery of pyrazolopyrimidines as the first class of allosteric agonists for the high affinity nicotinic acid receptor GPR109A Bioorg. Med. Chem. Lett. 2008, 18, 4948-4951
    • (2008) Bioorg. Med. Chem. Lett. , vol.18 , pp. 4948-4951
    • Shen, H.C.1    Taggart, A.K.P.2    Wilsie, L.C.3    Waters, M.G.4    Hammond, M.L.5    Tata, J.R.6    Colletti, S.L.7
  • 12
    • 0020069535 scopus 로고
    • Synthesis and enzymic activity of 6-carbethoxy- and 6-ethoxy-3,7- disubstituted pyrazolo[1,5-a]pyrimidines and related derivatives as adenosine cyclic 3′,5′-phosphate phosphodiesterase inhibitors
    • Springer, R. H.; Scholten, M. B.; O'Brien, D. E.; Novinson, T.; Miller, J. P.; Robins, R. K. Synthesis and enzymic activity of 6-carbethoxy- and 6-ethoxy-3,7-disubstituted pyrazolo[1,5-a]pyrimidines and related derivatives as adenosine cyclic 3′,5′-phosphate phosphodiesterase inhibitors J. Med. Chem. 1982, 25, 235-242
    • (1982) J. Med. Chem. , vol.25 , pp. 235-242
    • Springer, R.H.1    Scholten, M.B.2    O'Brien, D.E.3    Novinson, T.4    Miller, J.P.5    Robins, R.K.6
  • 13
    • 84993880629 scopus 로고
    • Reactivity of 7-(2-dimethylaminovinyl)pyrazolo[1,5- a ]pyrimidines: Synthesis of pyrazolo[1,5- a ]pyrido[3,4- e ]pyrimidine derivatives as potential benzodiazepine receptor ligands. 2
    • Bruni, F.; Selleri, S.; Costanzo, A.; Guerrini, G.; Casilli, M. L.; Giusti, L. Reactivity of 7-(2-dimethylaminovinyl)pyrazolo[1,5- a ]pyrimidines: synthesis of pyrazolo[1,5- a ]pyrido[3,4- e ]pyrimidine derivatives as potential benzodiazepine receptor ligands. 2 J. Heterocycl. Chem. 1995, 32, 291-298
    • (1995) J. Heterocycl. Chem. , vol.32 , pp. 291-298
    • Bruni, F.1    Selleri, S.2    Costanzo, A.3    Guerrini, G.4    Casilli, M.L.5    Giusti, L.6
  • 17
    • 78149496159 scopus 로고    scopus 로고
    • Allosteric modulation of G protein-coupled receptors: A pharmacological perspective
    • Keov, P.; Sexton, P. M.; Christopoulos, A. Allosteric modulation of G protein-coupled receptors: a pharmacological perspective Neuropharmacology 2011, 60, 24-35
    • (2011) Neuropharmacology , vol.60 , pp. 24-35
    • Keov, P.1    Sexton, P.M.2    Christopoulos, A.3
  • 20
    • 0015861774 scopus 로고
    • Relationship between the inhibition constant (Ki) and the concentration of inhibitor which causes 50% inhibition (I50) of an enzymatic reaction
    • Cheng, Y.; Prusoff, W. H. Relationship between the inhibition constant (Ki) and the concentration of inhibitor which causes 50% inhibition (I50) of an enzymatic reaction Biochem. Pharmacol. 1973, 22, 3099-3108
    • (1973) Biochem. Pharmacol. , vol.22 , pp. 3099-3108
    • Cheng, Y.1    Prusoff, W.H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.