메뉴 건너뛰기




Volumn 5, Issue 5, 2002, Pages 749-755

Allosteric modulation of G protein-coupled receptors

Author keywords

Allosteric modulators; G protein coupled receptors; Positive and negative cooperativity

Indexed keywords

2 AMINO 4,5 DIMETHYL 3 (3 TRIFLUOROMETHYLBENZOYL)THIOPHENE; 2 AMINOTHIAZOLE DERIVATIVE; 2 CHLORO 6 [3 [1,1 DIMETHYL 2 (2 NAPHTHYL)ETHYLAMINO] 2 HYDROXYPROPOXY]BENZONITRILE; 2 METHYL 6 (2 PHENYLVINYL)PYRIDINE; 4 AMINOBUTYRIC ACID B RECEPTOR; 4 AMINOBUTYRIC ACID B RECEPTOR STIMULATING AGENT; 4 ANILINO 2 CYCLOPENTYLIMIDAZO[4,5 C]QUINOLINE; 4 METHOXY N [7 METHYL 3 (2 PYRIDINYL) 1 ISOQUINOLINYL]BENZAMIDE; 6 N CYCLOPENTYLADENOSINE; 8 CYCLOPENTYL 1,3 DIPROPYLXANTHINE; ADENOSINE A1 RECEPTOR; ADENOSINE A1 RECEPTOR AGONIST; ADENOSINE A1 RECEPTOR ANTAGONIST; ADENOSINE A3 RECEPTOR; ADENOSINE A3 RECEPTOR AGONIST; ADENOSINE A3 RECEPTOR ANTAGONIST; BAY 36 7620; CALCIUM CHANNEL STIMULATING AGENT; CALCIUM ION; CGP 7930; G PROTEIN COUPLED RECEPTOR; GLUTAMATE RECEPTOR; GLUTAMATE RECEPTOR ANTAGONIST; METHYLPHENYLETHYNYLPYRIDINE; MUSCARINIC RECEPTOR; N [3 (2 CHLOROPHENYL)PROPYL] 1 (3 METHOXYPHENYL)ETHYLAMINE; NEW DRUG; RECEPTOR SUBTYPE; T 7; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 0036771048     PISSN: 13676733     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (30)

References (50)
  • 1
    • 0034677966 scopus 로고    scopus 로고
    • Drug discovery: A historical perspective
    • Drews J: Drug discovery: A historical perspective. Science (2000) 287:1960-1964.
    • (2000) Science , vol.287 , pp. 1960-1964
    • Drews, J.1
  • 2
    • 73649152457 scopus 로고
    • Allosteric proteins and cellular control systems
    • Monod J, Changeux J-P, Jacob F: Allosteric proteins and cellular control systems. J Mol Biol (1963) 6:306-329.
    • (1963) J Mol Biol , vol.6 , pp. 306-329
    • Monod, J.1    Changeux, J.-P.2    Jacob, F.3
  • 3
    • 0035211686 scopus 로고    scopus 로고
    • Allosteric modulation of G-protein-coupled receptors
    • Soudijn W, Van Wijngaarden I, IJzerman AP: Allosteric modulation of G-protein-coupled receptors. Expert Opin Ther Patents (2001) 11:1889-1904. This paper should be read as an introduction to the current review.
    • (2001) Expert Opin Ther Patents , vol.11 , pp. 1889-1904
    • Soudijn, W.1    Van Wijngaarden, I.2    IJzerman, A.P.3
  • 4
    • 0036490942 scopus 로고    scopus 로고
    • Allosteric binding sites on cell-surface receptors: Novel targets for drug discovery
    • Christopoulos A: Allosteric binding sites on cell-surface receptors: Novel targets for drug discovery. Nat Rev Drug Disc (2002) 1:198-210. This paper gives a detailed account on allosteric modulation of GPCRs, including its 'mathematical' foundation.
    • (2002) Nat Rev Drug Disc , vol.1 , pp. 198-210
    • Christopoulos, A.1
  • 5
    • 0025603686 scopus 로고
    • 1 receptor binding and function by 2-amino-3-benzoylthiophenes
    • 1 receptor binding and function by 2-amino-3-benzoylthiophenes. Mol Pharmacol (1990) 38:939-949. This is a seminal paper on allosteric modulation of adenosine receptors.
    • (1990) Mol Pharmacol , vol.38 , pp. 939-949
    • Bruns, R.F.1    Fergus, J.H.2
  • 8
    • 0029895280 scopus 로고    scopus 로고
    • Effects of long-term treatment with the allosteric enhancer, PD81,723, on Chinese hamster ovary cells expressing recombinant human A, adenosine receptors
    • Bhattacharya S, Linden J: Effects of long-term treatment with the allosteric enhancer, PD81,723, on Chinese hamster ovary cells expressing recombinant human A, adenosine receptors. Mol Pharmacol (1996) 50:104-111.
    • (1996) Mol Pharmacol , vol.50 , pp. 104-111
    • Bhattacharya, S.1    Linden, J.2
  • 12
    • 0033539111 scopus 로고    scopus 로고
    • Allosteric modulation of the adenosine A, receptor. Synthesis and biological evaluation of novel 2-amino-3-benzoylthiophenes as allosteric enhancers of agonist binding
    • Van der Klein PA, Kourounakis AP, IJzerman AP: Allosteric modulation of the adenosine A, receptor. Synthesis and biological evaluation of novel 2-amino-3-benzoylthiophenes as allosteric enhancers of agonist binding. J Med Chem (1999) 42:3629-3636.
    • (1999) J Med Chem , vol.42 , pp. 3629-3636
    • Van der Klein, P.A.1    Kourounakis, A.P.2    IJzerman, A.P.3
  • 17
    • 0032808078 scopus 로고    scopus 로고
    • NPS R-568 A type II calcimimetic compound that acts on parathyroid cell calcium receptor of rats to reduce plasma levels of parathyroid hormone and calcium
    • Fox J, Lowe SH, Petty BA, Nemeth EF: NPS R-568: A type II calcimimetic compound that acts on parathyroid cell calcium receptor of rats to reduce plasma levels of parathyroid hormone and calcium. J Pharmacol Exp Ther (1999) 290:473-479.
    • (1999) J Pharmacol Exp Ther , vol.290 , pp. 473-479
    • Fox, J.1    Lowe, S.H.2    Petty, B.A.3    Nemeth, E.F.4
  • 19
    • 0033935152 scopus 로고    scopus 로고
    • A calcimimetic agent lowers plasma parathyroid hormone levels in patients with secondary hyperparathyroidism
    • Goodman WG, Frazão JM, Tumer SA, Goodkin DA, Liu W, Cobum JW: A calcimimetic agent lowers plasma parathyroid hormone levels in patients with secondary hyperparathyroidism. Kidney Int (2000) 58:436-445.
    • (2000) Kidney Int , vol.58 , pp. 436-445
    • Goodman, W.G.1    Frazão, J.M.2    Tumer, S.A.3    Goodkin, D.A.4    Liu, W.5    Cobum, J.W.6
  • 20
    • 0035999938 scopus 로고    scopus 로고
    • The calcimimetic agents: Perspectives for treatment
    • Frazão JM, Martins P, Cobum JW: The calcimimetic agents: Perspectives for treatment Kidney Int (2002) 61:S149-S154.
    • (2002) Kidney Int , vol.61
    • Frazão, J.M.1    Martins, P.2    Cobum, J.W.3
  • 24
    • 0036462446 scopus 로고    scopus 로고
    • Allosteric modulators of group I metabotropic glutamate receptors: Novel subtype-selective ligands and therapeutic perspectives
    • Gasparini F, Kuhn R, Pin JP: Allosteric modulators of group I metabotropic glutamate receptors: Novel subtype-selective ligands and therapeutic perspectives. Curr Opin Pharmacol (2002) 2:43-49.
    • (2002) Curr Opin Pharmacol , vol.2 , pp. 43-49
    • Gasparini, F.1    Kuhn, R.2    Pin, J.P.3
  • 28
    • 0034721795 scopus 로고    scopus 로고
    • The non-competitive antagonists 2-methyl-6-(phenylethynyl)-pyridine and 7-hydroxyiminocyclopropan[b] chromen-1a-carboxylic acid ethyl ester interact with overlapping binding pockets in the transmembrane region of group I metabotropic glutamate receptors
    • Pagano A, Ruegg D, Litschig S, Stoehr N, Stierlin C, Heinrich M, Floersheim P, Prézeau L, Carroll F, Pin JP, Cambria A et al. The non-competitive antagonists 2-methyl-6-(phenylethynyl)-pyridine and 7-hydroxyiminocyclopropan[b] chromen-1a-carboxylic acid ethyl ester interact with overlapping binding pockets in the transmembrane region of group I metabotropic glutamate receptors. J Biol Chem (2000) 275:33750-33758.
    • (2000) J Biol Chem , vol.275 , pp. 33750-33758
    • Pagano, A.1    Ruegg, D.2    Litschig, S.3    Stoehr, N.4    Stierlin, C.5    Heinrich, M.6    Floersheim, P.7    Prézeau, L.8    Carroll, F.9    Pin, J.P.10    Cambria, A.11
  • 31
    • 0034105111 scopus 로고    scopus 로고
    • Anticonvulsant activity of two metabotropic glutamate group I antagonists selective for the mGlu5 receptor: 2-methyl-6-(phenylethynyl)-pyridine (MPEP), and (E)-6-methyl-2-styrylpyridine (SIB 1893)
    • Chapman AG, Nanan K, Williams M, Meldrum BS: Anticonvulsant activity of two metabotropic glutamate group I antagonists selective for the mGlu5 receptor: 2-methyl-6- (phenylethynyl)-pyridine (MPEP), and (E)-6-methyl-2-styrylpyridine (SIB 1893). Neuropharmacology (2000) 39:1567-1574.
    • (2000) Neuropharmacology , vol.39 , pp. 1567-1574
    • Chapman, A.G.1    Nanan, K.2    Williams, M.3    Meldrum, B.S.4
  • 32
    • 0033680311 scopus 로고    scopus 로고
    • Anxiolytic-like effects of the prototypical metabotropic glutamate receptor 5 antagonist 2-methyl-6-(phenylethynyl)pyridine in rodents
    • Spooren WP, Vassout A, Neijt HC, Kuhn R, Gasparini F, Roux S, Porsolt RD, Gentsch C: Anxiolytic-like effects of the prototypical metabotropic glutamate receptor 5 antagonist 2-methyl-6-(phenylethynyl)pyridine in rodents. J Pharmacol Exp Ther (2000) 295:1267-1275.
    • (2000) J Pharmacol Exp Ther , vol.295 , pp. 1267-1275
    • Spooren, W.P.1    Vassout, A.2    Neijt, H.C.3    Kuhn, R.4    Gasparini, F.5    Roux, S.6    Porsolt, R.D.7    Gentsch, C.8
  • 33
    • 0035069188 scopus 로고    scopus 로고
    • Potential anxiolytic- and antidepressant-like effects of MPEP, a potent, selective and systemically active mGlu5 receptor antagonist
    • Tatarczynska E, Klodzinska A, Chojnacka-Wojcik E, Palucha A, Gasparini F, Kuhn R, Pilc A: Potential anxiolytic- and antidepressant-like effects of MPEP, a potent, selective and systemically active mGlu5 receptor antagonist. Br J Pharmacol (2001) 132:1423-1430.
    • (2001) Br J Pharmacol , vol.132 , pp. 1423-1430
    • Tatarczynska, E.1    Klodzinska, A.2    Chojnacka-Wojcik, E.3    Palucha, A.4    Gasparini, F.5    Kuhn, R.6    Pilc, A.7
  • 34
    • 0034968969 scopus 로고    scopus 로고
    • The metabotropic glutamate receptor antagonist 2-methyl-6-(phenylethynyl)-pyridine (MPEP) blocks fear conditioning in rats
    • Schulz B, Fendt M, Gasparini F, Lingenhöhl K, Kuhn R, Koch M: The metabotropic glutamate receptor antagonist 2-methyl-6-(phenylethynyl)-pyridine (MPEP) blocks fear conditioning in rats. Neuropharmacology (2001) 41:1-7.
    • (2001) Neuropharmacology , vol.41 , pp. 1-7
    • Schulz, B.1    Fendt, M.2    Gasparini, F.3    Lingenhöhl, K.4    Kuhn, R.5    Koch, M.6
  • 35
    • 0034868541 scopus 로고    scopus 로고
    • Blockade of the metabotropic glutamate receptor subtype 5 (mGluR5) produces antiparkinsonian-like effects in rats
    • Ossowska K, Konieczny J, Wolfarth S, Wieronska J, Pilc A: Blockade of the metabotropic glutamate receptor subtype 5 (mGluR5) produces antiparkinsonian-like effects in rats. Neuropharmacology (2001) 41:413-420.
    • (2001) Neuropharmacology , vol.41 , pp. 413-420
    • Ossowska, K.1    Konieczny, J.2    Wolfarth, S.3    Wieronska, J.4    Pilc, A.5
  • 39
    • 0034757740 scopus 로고    scopus 로고
    • B receptors open new routes for the development of drugs targeting family 3 G-protein-coupled receptors
    • B receptors open new routes for the development of drugs targeting family 3 G-protein-coupled receptors. Mol Pharmacol (2001) 60:881-884.
    • (2001) Mol Pharmacol , vol.60 , pp. 881-884
    • Pin, J.P.1    Parmentier, M.L.2    Prézeau, L.3
  • 40
    • 0034760504 scopus 로고    scopus 로고
    • B receptors by 2,6-di-tert-butyl-4-(3-hydroxy-2,2-dimethylpropyl)-phenol (CGP7930) and its aldehyde analog CGP13501
    • Urwyler S, Mosbacher J, Lingenhöhl K, Heid J, Hofstetter K, Froestl W, Bettler B, Kaupmann K: Positive allosteric modulation of native and recombinant y-aminobutyric acid. receptors by 2,6-di-tert-butyl-4-(3-hydroxy-2,2-dimethylpropyl)-phenol (CGP7930) and its aldehyde analog CGP13501. Mol Pharmacol (2001) 60:963-971.
    • (2001) Mol Pharmacol , vol.60 , pp. 963-971
    • Urwyler, S.1    Mosbacher, J.2    Lingenhöhl, K.3    Heid, J.4    Hofstetter, K.5    Froestl, W.6    Bettler, B.7    Kaupmann, K.8
  • 42
    • 0013349204 scopus 로고    scopus 로고
    • Allosteric adenosine receptor modulators. WO-09921617 (1999)
    • MEDCO RESEARCH INC (Baraldi PG): Allosteric adenosine receptor modulators. WO-09921617 (1999).
    • Baraldi, P.G.1
  • 43
    • 0013348848 scopus 로고    scopus 로고
    • Thiophenes useful for modulating the adenosine receptor. US-05939432 (1999)
    • MEDCO RESEARCH INC (Baraldi PG): Thiophenes useful for modulating the adenosine receptor. US-05939432 (1999).
    • Baraldi, P.G.1
  • 44
    • 0013393271 scopus 로고    scopus 로고
    • Allosteric adenosine receptor modulators. US-06177444 (2001)
    • MEDCO RESEARCH INC (Baraldi PG): Allosteric adenosine receptor modulators. US-06177444 (2001).
    • Baraldi, P.G.1
  • 45
    • 0013398118 scopus 로고    scopus 로고
    • Allosteric adenosine receptor modulators. US-06194449 (2001)
    • MEDCO RESEARCH INC (Baraldi PG): Allosteric adenosine receptor modulators. US-06194449 (2001).
    • Baraldi, P.G.1
  • 48
    • 0013401210 scopus 로고    scopus 로고
    • Heterocyclic compounds, their preparation and their therapeutic use. US-05877199 (1999)
    • SANKYO CO LTD (Birdsall N, Lazareno S, Naruto S, Sugimoto M, Koyamo K, Marumoto S): Heterocyclic compounds, their preparation and their therapeutic use. US-05877199 (1999).
    • Birdsall, N.1    Lazareno, S.2    Naruto, S.3    Sugimoto, M.4    Koyamo, K.5    Marumoto, S.6
  • 49
    • 0013392699 scopus 로고    scopus 로고
    • Heterocyclic compounds, useful as allosteric effectors at muscarinic receptors. WO-09603377 (1996)
    • SANKYO CO LTD (Birdsall N, Lazareno S, Naruto S, Sugimoto M, Koyama K, Marumoto S): Heterocyclic compounds, useful as allosteric effectors at muscarinic receptors. WO-09603377 (1996).
    • Birdsall, N.1    Lazareno, S.2    Naruto, S.3    Sugimoto, M.4    Koyama, K.5    Marumoto, S.6
  • 50
    • 0013345652 scopus 로고    scopus 로고
    • Allosteric effectors at muscarinic receptors. GB-02292685 (1996)
    • SANKYO CO LTD (Hiraoka T, Birdsall N, Gharagozloo P, Lazareno S): Allosteric effectors at muscarinic receptors. GB-02292685 (1996).
    • Hiraoka, T.1    Birdsall, N.2    Gharagozloo, P.3    Lazareno, S.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.