메뉴 건너뛰기




Volumn 39, Issue 3-4, 1996, Pages 289-300

Recent developments in selective agonists and antagonists acting at purine and pyrimidine receptors

Author keywords

Adenosine; Agonists; Antagonists; ATP; Structure activity relationships; Xanthines

Indexed keywords

4 [2 [7 AMINO 2 (2 FURYL) 1,2,4 TRIAZOLO[2,3 A][1,3,5]TRIAZIN 5 YLAMINO]ETHYL]PHENOL; 5 AMINO 2 (2 FURYL) 7 (2 PHENYLETHYL)PYRAZOLO[4,3 E][1,2,4]TRIAZOLO[1,5 C]PYRIMIDINE; ADENOSINE DERIVATIVE; ADENOSINE RECEPTOR BLOCKING AGENT; ADENOSINE RECEPTOR STIMULATING AGENT; PURINE RECEPTOR; RECEPTOR SUBTYPE; SURAMIN; THEOPHYLLINE;

EID: 0030441568     PISSN: 02724391     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-2299(199611/12)39:3/4<289::AID-DDR8>3.0.CO;2-N     Document Type: Conference Paper
Times cited : (59)

References (70)
  • 12
    • 0029892771 scopus 로고    scopus 로고
    • A unifying purinergic hypothesis for the initiation of pain
    • Burnstock C (1996) A unifying purinergic hypothesis for the initiation of pain. Lancet 347:1604-1605.
    • (1996) Lancet , vol.347 , pp. 1604-1605
    • Burnstock, C.1
  • 15
    • 12644291447 scopus 로고    scopus 로고
    • Suramin and PPADS antagonists at transfected P2Y1, P2Y2, P2Y3, and P2Y4 receptors
    • Charlton S, Brown CA, Boarder MR (1996): Suramin and PPADS antagonists at transfected P2Y1, P2Y2, P2Y3, and P2Y4 receptors. Drug Dev Res 37:113.
    • (1996) Drug Dev Res , vol.37 , pp. 113
    • Charlton, S.1    Brown, C.A.2    Boarder, M.R.3
  • 16
    • 0028944887 scopus 로고
    • Differentiation by pyridoxal 5-phosphate, PPADS and isoPPADS between responses mediated by UTP and those evoked by α,β-methylenc-ATP on rat sympathetic-ganglia
    • Connolly GP (1995) Differentiation by pyridoxal 5-phosphate, PPADS and isoPPADS between responses mediated by UTP and those evoked by α,β-methylenc-ATP on rat sympathetic-ganglia. Br J Pharmacol 114:727-731.
    • (1995) Br J Pharmacol , vol.114 , pp. 727-731
    • Connolly, G.P.1
  • 18
    • 0003680332 scopus 로고
    • Structure activity relationships for adenine nucleotide receptors on mast cells, human platelets, and smooth muscle
    • Jacobson KA, Daly JW, Manganiello V (eds): New York: Springer
    • Cusack NJ, Hourani SMO (1990): Structure activity relationships for adenine nucleotide receptors on mast cells, human platelets, and smooth muscle. In Jacobson KA, Daly JW, Manganiello V (eds): Purines in Cellular Signalling: Targets for New Drugs. New York: Springer, pp. 254-259.
    • (1990) Purines in Cellular Signalling: Targets for New Drugs , pp. 254-259
    • Cusack, N.J.1    Hourani, S.M.O.2
  • 20
    • 0011444927 scopus 로고    scopus 로고
    • Structure, pharmacological selectivity and second messenger properties of G protein coupled P2 purinergic receptors
    • Jacobson KA, Jarvis MF (eels): New York: Wiley (in press)
    • Filtz TM, Harden TK, Nicholas RA (1997): Structure, pharmacological selectivity and second messenger properties of G protein coupled P2 purinergic receptors. In Jacobson KA, Jarvis MF (eels): Purinergic Approaches in Experimental Therapeutics. New York: Wiley (in press).
    • (1997) Purinergic Approaches in Experimental Therapeutics
    • Filtz, T.M.1    Harden, T.K.2    Nicholas, R.A.3
  • 25
    • 0026610760 scopus 로고
    • 2A adenosine receptors from rat striatum and rat pheochromocytoma PC12 cells: Characterization with radioligand binding and by activation of adenylate cyclase
    • 2A adenosine receptors from rat striatum and rat pheochromocytoma PC12 cells: Characterization with radioligand binding and by activation of adenylate cyclase. Mol Pharmacol 41:352-359.
    • (1992) Mol Pharmacol , vol.41 , pp. 352-359
    • Hide, I.1    Padgett, W.L.2    Jacobson, K.A.3    Daly, J.W.4
  • 26
    • 12644265871 scopus 로고    scopus 로고
    • P2T-purinoceptor antagonists: A novel class of anti-thrombotic agents
    • Humphries RG, Leff R Robertson MJ (1996): P2T-purinoceptor antagonists: A novel class of anti-thrombotic agents. Dnig Dev Res 37:175.
    • (1996) Dnig Dev Res , vol.37 , pp. 175
    • Humphries, R.G.1    Leff, R.2    Robertson, M.J.3
  • 28
    • 0026520040 scopus 로고
    • Perspective. Adenosine receptors: Pharmacology, structure-activity relationships and therapeutic potential
    • Jacobson KA, van Galen PJM, Williams M (1992a): Perspective. Adenosine receptors: Pharmacology, structure-activity relationships and therapeutic potential. J Med Chem 35:407-422.
    • (1992) J Med Chem , vol.35 , pp. 407-422
    • Jacobson, K.A.1    Van Galen, P.J.M.2    Williams, M.3
  • 33
    • 0030051539 scopus 로고    scopus 로고
    • Interactions of flavonoids and other phytochemicals with adenosine receptors
    • Ji XD, Melman N, Jacobson KA (1996): Interactions of flavonoids and other phytochemicals with adenosine receptors. J Med Chem 39:781-788.
    • (1996) J Med Chem , vol.39 , pp. 781-788
    • Ji, X.D.1    Melman, N.2    Jacobson, K.A.3
  • 36
    • 0028988643 scopus 로고
    • 2X purinoceptors be classified pharmacologically
    • 2X purinoceptors be classified pharmacologically. Trends Pharmacol Sci 16:168-174.
    • (1995) Trends Pharmacol Sci , vol.16 , pp. 168-174
    • Kennedy, C.1    Leff, P.2
  • 46
    • 0007298114 scopus 로고    scopus 로고
    • DMPX (3,7-dimethyl-1-propargylxanthine) derivatives: Structure activity relationships of potent selective A2a-adenosine receptor antagonists
    • Müller CE, Hipp J, Knoblauch B, Schobert U, Sauer R, Geis U (1996): DMPX (3,7-dimethyl-1-propargylxanthine) derivatives: Structure activity relationships of potent selective A2a-adenosine receptor antagonists. Drug Dev Res 37:112.
    • (1996) Drug Dev Res , vol.37 , pp. 112
    • Müller, C.E.1    Hipp, J.2    Knoblauch, B.3    Schobert, U.4    Sauer, R.5    Geis, U.6
  • 52
    • 0025306964 scopus 로고
    • 4-Amino[1,2,4]triazolo[4,3-a]quinoxalines. A novel class of potent adenosine receptor antagonists and potential rapid-onset antidepressants
    • Sarges R, Howard HR, Browne RG, Lebel LA, Seymour PA, Koe BK (1990): 4-Amino[1,2,4]triazolo[4,3-a]quinoxalines. A novel class of potent adenosine receptor antagonists and potential rapid-onset antidepressants. J Med Chem 33:2240-2254.
    • (1990) J Med Chem , vol.33 , pp. 2240-2254
    • Sarges, R.1    Howard, H.R.2    Browne, R.G.3    Lebel, L.A.4    Seymour, P.A.5    Koe, B.K.6
  • 54
    • 0026690401 scopus 로고
    • (E)-1,3-Dialkyl-7-methyl-8-(3,4,5-Trimethoxystyryl)xanthines: Potent and selective adenosine-A2 antagonists
    • Shimada J, Suzuki F, Nonaka H, Ishii A, Ichikawa S (1992): (E)-1,3-Dialkyl-7-methyl-8-(3,4,5-Trimethoxystyryl)xanthines: Potent and selective adenosine-A2 antagonists. J Med Chem 35:2342-2345.
    • (1992) J Med Chem , vol.35 , pp. 2342-2345
    • Shimada, J.1    Suzuki, F.2    Nonaka, H.3    Ishii, A.4    Ichikawa, S.5
  • 68
    • 0029142647 scopus 로고
    • Inhibitory action of PPADS on relaxant responses to adenine-nucleotides or electrical-field stimulation in guinea-pig taenia-coli and rat duodenum
    • Windscheif U, Pfaff O, Ziganshin AU, Hoyle CHV, Bäumert HG, Mutschler E, Burnstock C, Lambrecht G (1995): Inhibitory action of PPADS on relaxant responses to adenine-nucleotides or electrical-field stimulation in guinea-pig taenia-coli and rat duodenum. Br J Pharmacol 115:1509-1517.
    • (1995) Br J Pharmacol , vol.115 , pp. 1509-1517
    • Windscheif, U.1    Pfaff, O.2    Ziganshin, A.U.3    Hoyle, C.H.V.4    Bäumert, H.G.5    Mutschler, E.6    Burnstock, C.7    Lambrecht, G.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.