메뉴 건너뛰기




Volumn 68, Issue 2, 2005, Pages 393-402

Identification of indole derivatives exclusively interfering with a G protein-independent signaling pathway of the prostaglandin D2 receptor CRTH2

Author keywords

[No Author keywords available]

Indexed keywords

1 (4 ETHOXYPHENYL) 5 METHOXY 2 METHYLINDOLE 3 CARBOXYLIC ACID; CHEMOATTRACTANT RECEPTOR HOMOLOGOUS MOLECULE EXPRESSED ON TH2 CELL; GUANINE NUCLEOTIDE BINDING PROTEIN; INDOLE DERIVATIVE; INDOMETACIN; N ALPHA TOSYLTRYPTOPHAN; PROSTAGLANDIN D2; PROSTAGLANDIN RECEPTOR; RAMATROBAN; RETINA S ANTIGEN; TRITIUM; UNCLASSIFIED DRUG;

EID: 23044460265     PISSN: 0026895X     EISSN: None     Source Type: Journal    
DOI: 10.1124/mol.104.010520     Document Type: Article
Times cited : (91)

References (38)
  • 1
    • 0009644628 scopus 로고
    • Some quantitative uses of drug antagonists
    • Arunlakshana O and Schild HO (1959) Some quantitative uses of drug antagonists. Br J Pharmacol 14:48-58.
    • (1959) Br J Pharmacol , vol.14 , pp. 48-58
    • Arunlakshana, O.1    Schild, H.O.2
  • 2
    • 1342323325 scopus 로고    scopus 로고
    • Application of a kinetic model to the apparently complex behavior of negative and positive allosteric modulators of muscarinic acetylcholine receptors
    • Avlani V, May LT, Sexton PM, and Christopoulos A (2004) Application of a kinetic model to the apparently complex behavior of negative and positive allosteric modulators of muscarinic acetylcholine receptors. J Pharmacol Exp Ther 308:1062-1072.
    • (2004) J Pharmacol Exp Ther , vol.308 , pp. 1062-1072
    • Avlani, V.1    May, L.T.2    Sexton, P.M.3    Christopoulos, A.4
  • 3
    • 0141593597 scopus 로고    scopus 로고
    • β-Arrestin-mediated activation of MAPK by inverse agonists reveals distinct active conformations for G protein-coupled receptors
    • Azzi M, Charest PG, Angers S, Rousseau G, Kohout T, Bouvier M, and Pineyro G (2003) β-Arrestin-mediated activation of MAPK by inverse agonists reveals distinct active conformations for G protein-coupled receptors. Proc Natl Acad Sci USA 100:11406-11411.
    • (2003) Proc Natl Acad Sci USA , vol.100 , pp. 11406-11411
    • Azzi, M.1    Charest, P.G.2    Angers, S.3    Rousseau, G.4    Kohout, T.5    Bouvier, M.6    Pineyro, G.7
  • 4
    • 0345735773 scopus 로고    scopus 로고
    • Agonist and inverse agonist actions of β-blockers at the human β2-adrenoceptor provide evidence for agonist-directed signaling
    • Baker JG, Hall IP, and Hill SJ (2003) Agonist and inverse agonist actions of β-blockers at the human β2-adrenoceptor provide evidence for agonist-directed signaling. Mol Pharmacol 64:1357-1369.
    • (2003) Mol Pharmacol , vol.64 , pp. 1357-1369
    • Baker, J.G.1    Hall, I.P.2    Hill, S.J.3
  • 6
    • 10744227854 scopus 로고    scopus 로고
    • 11-Dehydro-thromboxane B2, a stable thromboxane metabolite, is a full agonist of chemoattractant receptorhomologous molecule expressed on TH2 cells (CRTH2) in human eosinophils and basophils
    • Bohm E, Sturm GJ, Weiglhofer I, Sandig H, Shichijo M, McNamee A, Pease JE, Kollroser M, Peskar BA, and Heinemann A (2004) 11-Dehydro-thromboxane B2, a stable thromboxane metabolite, is a full agonist of chemoattractant receptorhomologous molecule expressed on TH2 cells (CRTH2) in human eosinophils and basophils. J Biol Chem 279:7663-7670.
    • (2004) J Biol Chem , vol.279 , pp. 7663-7670
    • Bohm, E.1    Sturm, G.J.2    Weiglhofer, I.3    Sandig, H.4    Shichijo, M.5    McNamee, A.6    Pease, J.E.7    Kollroser, M.8    Peskar, B.A.9    Heinemann, A.10
  • 7
    • 0036258990 scopus 로고    scopus 로고
    • G protein-coupled receptor allosterism and complexing
    • Christopoulos A and Kenakin T (2002) G protein-coupled receptor allosterism and complexing. Pharmacol Rev 54:323-374.
    • (2002) Pharmacol Rev , vol.54 , pp. 323-374
    • Christopoulos, A.1    Kenakin, T.2
  • 8
    • 0035101820 scopus 로고    scopus 로고
    • Evolving concepts in G protein-coupled receptor endocytosis: The role in receptor desensitization and signaling
    • Ferguson SS (2001) Evolving concepts in G protein-coupled receptor endocytosis: the role in receptor desensitization and signaling. Pharmacol Rev 53:1-24.
    • (2001) Pharmacol Rev , vol.53 , pp. 1-24
    • Ferguson, S.S.1
  • 9
    • 0346996805 scopus 로고    scopus 로고
    • Allosteric enhancers of A1 adenosine receptors increase receptor-G protein coupling and counteract guanine nucleotide effects on agonist binding
    • Figler H, Olsson RA, and Linden J (2003) Allosteric enhancers of A1 adenosine receptors increase receptor-G protein coupling and counteract guanine nucleotide effects on agonist binding. Mol Pharmacol 64:1557-1564.
    • (2003) Mol Pharmacol , vol.64 , pp. 1557-1564
    • Figler, H.1    Olsson, R.A.2    Linden, J.3
  • 11
    • 0036088519 scopus 로고    scopus 로고
    • Selective allosteric enhancement of agonist binding and function at human A3 adenosine receptors by a series of imidazoquinoline derivatives
    • Gao ZG, Kim SG, Soltysiak KA, Melman N, IJzerman AP, and Jacobson KA (2002) Selective allosteric enhancement of agonist binding and function at human A3 adenosine receptors by a series of imidazoquinoline derivatives. Mol Pharmacol 62:81-89.
    • (2002) Mol Pharmacol , vol.62 , pp. 81-89
    • Gao, Z.G.1    Kim, S.G.2    Soltysiak, K.A.3    Melman, N.4    Ijzerman, A.P.5    Jacobson, K.A.6
  • 12
    • 3042630989 scopus 로고    scopus 로고
    • Functional selectivity of D2 receptor ligands in a Chinese hamster ovary HD2L cell line: Evidence for induction of ligand-specific receptor states
    • Gay EA, Urban JD, Nichols DE, Oxford GS, and Mailman RB (2004) Functional selectivity of D2 receptor ligands in a Chinese hamster ovary HD2L cell line: evidence for induction of ligand-specific receptor states. Mol Pharmacol 66:97-105.
    • (2004) Mol Pharmacol , vol.66 , pp. 97-105
    • Gay, E.A.1    Urban, J.D.2    Nichols, D.E.3    Oxford, G.S.4    Mailman, R.B.5
  • 14
    • 0842331059 scopus 로고    scopus 로고
    • The molecular acrobatics of arrestin activation
    • Gurevich VV and Gurevich EV (2004) The molecular acrobatics of arrestin activation. Trends Pharmacol Sci 25:105-111.
    • (2004) Trends Pharmacol Sci , vol.25 , pp. 105-111
    • Gurevich, V.V.1    Gurevich, E.V.2
  • 15
    • 14944363741 scopus 로고    scopus 로고
    • Structural determinants of arylacetic acid nonsteroidal anti-inflammatory drugs necessary for binding and activation of the prostaglandin D2 receptor CRTH2
    • Hata AN, Lybrand TP, Marnett LJ, and Breyer RM (2005) Structural determinants of arylacetic acid nonsteroidal anti-inflammatory drugs necessary for binding and activation of the prostaglandin D2 receptor CRTH2. Mol Pharmacol 67:640-647.
    • (2005) Mol Pharmacol , vol.67 , pp. 640-647
    • Hata, A.N.1    Lybrand, T.P.2    Marnett, L.J.3    Breyer, R.M.4
  • 16
    • 0036467346 scopus 로고    scopus 로고
    • Cutting edge: Agonistic effect of indomethacin on a prostaglandin D2 receptor, CRTH2
    • Hirai H, Tanaka K, Takano S, Ichimasa M, Nakamura M, and Nagata K (2002) Cutting edge: agonistic effect of indomethacin on a prostaglandin D2 receptor, CRTH2. J Immunol 168:981-985.
    • (2002) J Immunol , vol.168 , pp. 981-985
    • Hirai, H.1    Tanaka, K.2    Takano, S.3    Ichimasa, M.4    Nakamura, M.5    Nagata, K.6
  • 17
    • 0035862329 scopus 로고    scopus 로고
    • Prostaglandin D2 selectively induces chemotaxis in T helper type 2 cells, eosinophils and basophils via seventransmembrane receptor CRTH2
    • Hirai H, Tanaka K, Yoshie O, Ogawa K, Kenmotsu K, Takamori Y, Ichimasa M, Sugamura K, Nakamura M, Takano S, et al. (2001) Prostaglandin D2 selectively induces chemotaxis in T helper type 2 cells, eosinophils and basophils via seventransmembrane receptor CRTH2. J Exp Med 193:255-261.
    • (2001) J Exp Med , vol.193 , pp. 255-261
    • Hirai, H.1    Tanaka, K.2    Yoshie, O.3    Ogawa, K.4    Kenmotsu, K.5    Takamori, Y.6    Ichimasa, M.7    Sugamura, K.8    Nakamura, M.9    Takano, S.10
  • 18
    • 1442284465 scopus 로고    scopus 로고
    • Allosteric modulation of G-protein coupled receptors
    • Jensen AA and Spalding TA (2004) Allosteric modulation of G-protein coupled receptors. Eur J Pharm Sci 21:407-420.
    • (2004) Eur J Pharm Sci , vol.21 , pp. 407-420
    • Jensen, A.A.1    Spalding, T.A.2
  • 19
    • 0035083109 scopus 로고    scopus 로고
    • Inverse, protean and ligand-selective agonism: Matters of receptor conformation
    • Kenakin T (2001) Inverse, protean and ligand-selective agonism: matters of receptor conformation. FASEB J 15:598-611.
    • (2001) FASEB J , vol.15 , pp. 598-611
    • Kenakin, T.1
  • 20
    • 0043235844 scopus 로고    scopus 로고
    • Ligand-selective receptor conformations revisited: The promise and the problem
    • Kenakin T (2003) Ligand-selective receptor conformations revisited: the promise and the problem. Trends Pharmacol Sci 24:346-354.
    • (2003) Trends Pharmacol Sci , vol.24 , pp. 346-354
    • Kenakin, T.1
  • 21
    • 1942517868 scopus 로고    scopus 로고
    • Principles: Receptor theory in pharmacology
    • Kenakin T (2004) Principles: receptor theory in pharmacology. Trends Pharmacol Sci 25:186-192.
    • (2004) Trends Pharmacol Sci , vol.25 , pp. 186-192
    • Kenakin, T.1
  • 22
    • 0035497743 scopus 로고    scopus 로고
    • Is Galpha16 the optimal tool for fishing ligands of orphan Gprotein-coupled receptors?
    • Kostenis E (2001) Is Galpha16 the optimal tool for fishing ligands of orphan Gprotein-coupled receptors? Trends Pharmacol Sci 22:560-564.
    • (2001) Trends Pharmacol Sci , vol.22 , pp. 560-564
    • Kostenis, E.1
  • 24
    • 0030218059 scopus 로고    scopus 로고
    • Two-point kinetic experiments to quantify allosteric effects on radioligand dissociation
    • Kostenis E and Mohr K (1996) Two-point kinetic experiments to quantify allosteric effects on radioligand dissociation. Trends Pharmacol Sci 17:280-283.
    • (1996) Trends Pharmacol Sci , vol.17 , pp. 280-283
    • Kostenis, E.1    Mohr, K.2
  • 25
    • 0035577682 scopus 로고    scopus 로고
    • Modelling of promiscuous receptor-Gi/Gs-protein coupling and effector response
    • Kukkonen JP, Nasman J, and Akerman KE (2001) Modelling of promiscuous receptor-Gi/Gs-protein coupling and effector response. Trends Pharmacol Sci 22:616-622.
    • (2001) Trends Pharmacol Sci , vol.22 , pp. 616-622
    • Kukkonen, J.P.1    Nasman, J.2    Akerman, K.E.3
  • 26
    • 0036674605 scopus 로고    scopus 로고
    • Towards a high-affinity allosteric enhancer at muscarinic M1 receptors
    • Lazareno S, Popham A, and Birdsall NJ (2002) Towards a high-affinity allosteric enhancer at muscarinic M1 receptors. J Mol Neurosci 19:123-127.
    • (2002) J Mol Neurosci , vol.19 , pp. 123-127
    • Lazareno, S.1    Popham, A.2    Birdsall, N.J.3
  • 27
    • 0036473397 scopus 로고    scopus 로고
    • The role of beta-arrestins in the termination and transduction of G-protein-coupled receptor signals
    • Luttrell LM and Lefkowitz RJ (2002) The role of beta-arrestins in the termination and transduction of G-protein-coupled receptor signals. J Cell Sci 115:455-465.
    • (2002) J Cell Sci , vol.115 , pp. 455-465
    • Luttrell, L.M.1    Lefkowitz, R.J.2
  • 28
    • 0035478746 scopus 로고    scopus 로고
    • Protein-protein interactions at G protein-coupled receptors
    • Milligan G and White JH (2001) Protein-protein interactions at G protein-coupled receptors. Trends Pharmacol Sci 22:513-518.
    • (2001) Trends Pharmacol Sci , vol.22 , pp. 513-518
    • Milligan, G.1    White, J.H.2
  • 29
    • 2542637961 scopus 로고    scopus 로고
    • Development of a new type of allosteric modulator of muscarinic receptors: Hybrids of the antagonist AF-DX 384 and the hexamethonio derivative W84
    • Mohr M, Heller E, Ataie A, Mohr K, and Holzgrabe U (2004) Development of a new type of allosteric modulator of muscarinic receptors: hybrids of the antagonist AF-DX 384 and the hexamethonio derivative W84. J Med Chem 47:3324-3327.
    • (2004) J Med Chem , vol.47 , pp. 3324-3327
    • Mohr, M.1    Heller, E.2    Ataie, A.3    Mohr, K.4    Holzgrabe, U.5
  • 30
    • 0037435052 scopus 로고    scopus 로고
    • Systematic development of high affinity bis(ammonio)alkane-type allosteric enhancers of muscarinic ligand binding
    • Muth M, Bender W, Scharfenstein O, Holzgrabe U, Balatkova E, Trankle C, and Mohr K (2003) Systematic development of high affinity bis(ammonio)alkane- type allosteric enhancers of muscarinic ligand binding. J Med Chem 46:1031-1040.
    • (2003) J Med Chem , vol.46 , pp. 1031-1040
    • Muth, M.1    Bender, W.2    Scharfenstein, O.3    Holzgrabe, U.4    Balatkova, E.5    Trankle, C.6    Mohr, K.7
  • 35
    • 0037382497 scopus 로고    scopus 로고
    • An orally bioavailable small molecule antagonist of CRTH2, ramatroban (BAY U3405), inhibits prostaglandin D2-induced eosinophil migration in vitro
    • Sugimoto H, Shichijo M, Iino T, Manabe Y, Watanabe A, Shimazaki M, Gantner F, and Bacon KB (2003) An orally bioavailable small molecule antagonist of CRTH2, ramatroban (BAY U3405), inhibits prostaglandin D2-induced eosinophil migration in vitro. J Pharmacol Exp Ther 305:347-352.
    • (2003) J Pharmacol Exp Ther , vol.305 , pp. 347-352
    • Sugimoto, H.1    Shichijo, M.2    Iino, T.3    Manabe, Y.4    Watanabe, A.5    Shimazaki, M.6    Gantner, F.7    Bacon, K.B.8
  • 36
    • 1242276192 scopus 로고    scopus 로고
    • Roles of G protein-coupled receptor dimerization
    • Terrillon S and Bouvier M (2004) Roles of G protein-coupled receptor dimerization. EMBO Rep 5:30-34.
    • (2004) EMBO Rep , vol.5 , pp. 30-34
    • Terrillon, S.1    Bouvier, M.2
  • 37
    • 13944263887 scopus 로고    scopus 로고
    • Minor structural modifications convert the dual TP/CRTH2 antagonist ramatroban into a highly selective and potent CRTH2 antagonist
    • Ulven T and Kostenis E (2005) Minor structural modifications convert the dual TP/CRTH2 antagonist ramatroban into a highly selective and potent CRTH2 antagonist. J Med Chem 48:897-900.
    • (2005) J Med Chem , vol.48 , pp. 897-900
    • Ulven, T.1    Kostenis, E.2
  • 38
    • 0141703263 scopus 로고    scopus 로고
    • Independent β-arrestin 2 and G protein-mediated pathways for angiotensin II activation of extracellular signal-regulated kinases 1 and 2
    • Wei H, Ahn S, Shenoy SK, Karnik SS, Hunyady L, Luttrell LM, and Lefkowitz RJ (2003) Independent β-arrestin 2 and G protein-mediated pathways for angiotensin II activation of extracellular signal-regulated kinases 1 and 2. Proc Natl Acad Sci USA 100:10782-10787.
    • (2003) Proc Natl Acad Sci USA , vol.100 , pp. 10782-10787
    • Wei, H.1    Ahn, S.2    Shenoy, S.K.3    Karnik, S.S.4    Hunyady, L.5    Luttrell, L.M.6    Lefkowitz, R.J.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.