-
1
-
-
0034677966
-
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
-
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
-
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
-
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
-
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
-
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
-
9
-
-
0033523421
-
1 receptor allosteric enhancer PD 81,723 on agonist binding to brain and adipocyte membranes
-
1 receptor allosteric enhancer PD 81,723 on agonist binding to brain and adipocyte membranes. Brain Res (1999) 840:75-83.
-
(1999)
Brain Res
, vol.840
, pp. 75-83
-
-
Jarvis, M.F.1
Gessner, G.2
Shapiro, G.3
Merkel, L.4
Myers, M.5
Cox, B.F.6
Martin, G.E.7
-
11
-
-
0037122790
-
1 adenosine receptors
-
1 adenosine receptors. J Med Chem (2002) 45:382-389.
-
(2002)
J Med Chem
, vol.45
, pp. 382-389
-
-
Tranberg, C.E.1
Zickgraf, A.2
Giunta, B.N.3
Luetjens, H.4
Figler, H.5
Murphree, L.J.6
Falke, R.7
Fleischer, H.8
Linden, J.9
Scammells, P.J.10
Olsson, R.A.11
-
12
-
-
0033539111
-
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
-
13
-
-
0037124178
-
2-Aminothiazoles: A new class of agonist allosteric enhancers of A, adenosine receptors
-
Chordia MD, Murphree LJ, Macdonald TL, Linden J, Olsson RA: 2-Aminothiazoles: A new class of agonist allosteric enhancers of A, adenosine receptors. Bioorg Med Chem Lett (2002) 12:1563-1566.
-
(2002)
Bioorg Med Chem Lett
, vol.12
, pp. 1563-1566
-
-
Chordia, M.D.1
Murphree, L.J.2
Macdonald, T.L.3
Linden, J.4
Olsson, R.A.5
-
16
-
-
0032584086
-
Calcimimetics with potent and selective activity on the parathyroid calcium receptor
-
Nemeth EF, Steffey ME, Hammerland LG, Hung BC, Van Wagenen BC, DelMar EG, Balandrin MF: Calcimimetics with potent and selective activity on the parathyroid calcium receptor. Proc Natl Acad Sci USA (1998) 95:4040-4045. This paper is the first disclosure of calcimimetics acting via allosteric mechanisms.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 4040-4045
-
-
Nemeth, E.F.1
Steffey, M.E.2
Hammerland, L.G.3
Hung, B.C.4
Van Wagenen, B.C.5
DelMar, E.G.6
Balandrin, M.F.7
-
17
-
-
0032808078
-
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
-
18
-
-
0031763613
-
Treatment of hypercalcemia secondary to parathyroid carcinoma with a novel calcimimetic agent
-
Collins MT, Skarulis MC, Bilezikian JP, Silverberg SJ, Spiegel AM, Marx SJ: Treatment of hypercalcemia secondary to parathyroid carcinoma with a novel calcimimetic agent J Clin Endocrinol Metab (1998) 83:1083-1088.
-
(1998)
J Clin Endocrinol Metab
, vol.83
, pp. 1083-1088
-
-
Collins, M.T.1
Skarulis, M.C.2
Bilezikian, J.P.3
Silverberg, S.J.4
Spiegel, A.M.5
Marx, S.J.6
-
19
-
-
0033935152
-
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
-
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
-
21
-
-
0036208986
-
The calcimimetic agent AMG 073 lowers plasma parathyroid hormone levels in hemodialysis patients with secondary hyperparathyroidism
-
Goodman WG, Hladik GA, Tumer SA, Blaisdell PW, Goodkin DA, Liu W, Bam YM, Cohen RM, Cobum JW: The calcimimetic agent AMG 073 lowers plasma parathyroid hormone levels in hemodialysis patients with secondary hyperparathyroidism. J Am Soc Nephrol (2002) 13:1017-1024.
-
(2002)
J Am Soc Nephrol
, vol.13
, pp. 1017-1024
-
-
Goodman, W.G.1
Hladik, G.A.2
Tumer, S.A.3
Blaisdell, P.W.4
Goodkin, D.A.5
Liu, W.6
Bam, Y.M.7
Cohen, R.M.8
Cobum, J.W.9
-
22
-
-
0034806606
-
2+ receptor antagonists that stimulate secretion of parathyroid hormone
-
2+ receptor antagonists that stimulate secretion of parathyroid hormone. J Pharmacol Exp Ther (2001) 299:323-331.
-
(2001)
J Pharmacol Exp Ther
, vol.299
, pp. 323-331
-
-
Nemeth, E.F.1
Delmar, E.G.2
Heaton, W.L.3
Miller, M.A.4
Lambert, L.D.5
Conklin, R.L.6
Gowen, M.7
Gleason, J.G.8
Bhatnagar, P.K.9
Fox, J.10
-
23
-
-
0034123554
-
Antagonizing the parathyroid calcium receptor stimulates parathyroid hormone secretion and bone formation in osteopenic rats
-
Gowen M, Stroup GB, Dodds RA, James IE, Votta BJ, Smith BR, Bhatnagar PK, Lago AM, Callahan JF, DelMar EG, Miller MA et al. Antagonizing the parathyroid calcium receptor stimulates parathyroid hormone secretion and bone formation in osteopenic rats. J Clin Invest (2000) 105:1595-1604.
-
(2000)
J Clin Invest
, vol.105
, pp. 1595-1604
-
-
Gowen, M.1
Stroup, G.B.2
Dodds, R.A.3
James, I.E.4
Votta, B.J.5
Smith, B.R.6
Bhatnagar, P.K.7
Lago, A.M.8
Callahan, J.F.9
DelMar, E.G.10
Miller, M.A.11
-
24
-
-
0036462446
-
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
-
25
-
-
0033028258
-
CPCCOET a noncompetitive metabotropic glutamate receptor 1 antagonist, inhibits receptor signaling without affecting glutamate binding
-
Litschig S, Gaspadni F, Rueegg D, Stoehr N, Flor PJ, Vranesic I, Prézeau L, Pin JP, Thomsen C, Kuhn R: CPCCOET a noncompetitive metabotropic glutamate receptor 1 antagonist, inhibits receptor signaling without affecting glutamate binding. Mol Pharmacol (1999) 55:453-461.
-
(1999)
Mol Pharmacol
, vol.55
, pp. 453-461
-
-
Litschig, S.1
Gaspadni, F.2
Rueegg, D.3
Stoehr, N.4
Flor, P.J.5
Vranesic, I.6
Prézeau, L.7
Pin, J.P.8
Thomsen, C.9
Kuhn, R.10
-
26
-
-
0035028011
-
Bay367620: A potent non-competitive mGlu1 receptor antagonist with inverse agonist activity
-
Carroll FY, Stolle A, Beart PM, Voerste A, Brabet I, Mauler F, Joly C, Antonicek H, Bockaert J, Müller T, Pin JP, Prézeau L: Bay367620: A potent non-competitive mGlu1 receptor antagonist with inverse agonist activity. Mol Pharmacol (2001) 59:965-973.
-
(2001)
Mol Pharmacol
, vol.59
, pp. 965-973
-
-
Carroll, F.Y.1
Stolle, A.2
Beart, P.M.3
Voerste, A.4
Brabet, I.5
Mauler, F.6
Joly, C.7
Antonicek, H.8
Bockaert, J.9
Müller, T.10
Pin, J.P.11
Prézeau, L.12
-
27
-
-
0032853255
-
2-Methyl-6-(phenylethynyl)-pyridine (MPEP), a potent, selective and systemically active mGlu5 receptor antagonist
-
Gasparini F, Lingenhöhl K, Stoehr N, Flor PJ, Heinrich M, Vranesic I, Biollaz M, Allgeier H, Heckendom R, Unwyler S, Varney MA et al. 2-Methyl-6-(phenylethynyl)-pyridine (MPEP), a potent, selective and systemically active mGlu5 receptor antagonist. Neuropharmacology (1999) 38:1493-1503.
-
(1999)
Neuropharmacology
, vol.38
, pp. 1493-1503
-
-
Gasparini, F.1
Lingenhöhl, K.2
Stoehr, N.3
Flor, P.J.4
Heinrich, M.5
Vranesic, I.6
Biollaz, M.7
Allgeier, H.8
Heckendom, R.9
Unwyler, S.10
Varney, M.A.11
-
28
-
-
0034721795
-
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
-
29
-
-
18244380874
-
3H]-M-MPEP, a potent, subtype-selective radioligand for the metabotropic glutamate receptor subtype 5
-
3H]-M-MPEP, a potent, subtype-selective radioligand for the metabotropic glutamate receptor subtype 5. Bioorg Med Chem Lett (2002) 12:407-409.
-
(2002)
Bioorg Med Chem Lett
, vol.12
, pp. 407-409
-
-
Gaspadni, F.1
Andres, H.2
Flor, P.J.3
Heinrich, M.4
Inderbitzin, W.5
Lingenhöhl, K.6
Müller, H.7
Munk, V.C.8
Omilusik, K.9
Stierlin, C.10
Stoehr, N.11
-
30
-
-
0013346618
-
Anticonvulsant activity in mice of BAY 36-7620, a novel, selective mgluR1 antagonist
-
New Orleans, LA, USA:Abs 618.10
-
Chapman AG, Nanan K, Meldrum BS, Schreiber R, De Vry J, Müller T: Anticonvulsant activity in mice of BAY 36-7620, a novel, selective mgluR1 antagonist. 30th Annual Meeting of the Society for Neuroscience, New Orleans, LA, USA (2000):Abs 618.10.
-
(2000)
30th Annual Meeting of the Society for Neuroscience
-
-
Chapman, A.G.1
Nanan, K.2
Meldrum, B.S.3
Schreiber, R.4
De Vry, J.5
Müller, T.6
-
31
-
-
0034105111
-
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
-
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
-
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
-
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
-
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
-
37
-
-
0034731374
-
B receptors
-
B receptors. J Biol Chem (2000) 275:41166-41174.
-
(2000)
J Biol Chem
, vol.275
, pp. 41166-41174
-
-
Galvez, T.1
Prezeau, L.2
Milioti, G.3
Franek, M.4
Joly, C.5
Froestl, W.6
Bettler, B.7
Bertrand, H.O.8
Blahos, J.9
Pin, J.P.10
-
38
-
-
0035341213
-
B receptor function
-
B receptor function. EMBO J (2001) 20:2152-2159. This study relates receptor heterodimedzation to allosteric modulation.
-
(2001)
EMBO J
, vol.20
, pp. 2152-2159
-
-
Galvez, T.1
Duthey, B.2
Kniazeff, J.3
Blahos, J.4
Rovelli, G.5
Bettler, B.6
Prézeau, L.7
Pin, J.P.8
-
39
-
-
0034757740
-
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
-
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
-
41
-
-
0033534392
-
4 muscarinic receptors
-
4 muscarinic receptors. Life Sci (1999) 64:519-526.
-
(1999)
Life Sci
, vol.64
, pp. 519-526
-
-
Lazareno, S.1
Birdsall, B.2
Fukazawa, P.3
Gharagozloo, P.4
Hashimoto, T.5
Kuwano, H.6
Popham, A.7
Sugimoto, M.8
Birdsall, N.J.9
-
42
-
-
0013349204
-
-
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
-
-
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
-
-
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
-
-
Allosteric adenosine receptor modulators. US-06194449 (2001)
-
MEDCO RESEARCH INC (Baraldi PG): Allosteric adenosine receptor modulators. US-06194449 (2001).
-
-
-
Baraldi, P.G.1
-
47
-
-
0013347138
-
-
Method of using calcilytic compounds. US-06022894 (2000)
-
NPS PHARMACEUTICALS INC (DelMar EG, Barmore RM, Sheehan D, van Wagenen BC, Callahan JF, Keenan RM, Kotecha NR, Lago MA, Southall LS, Thompson M): Method of using calcilytic compounds. US-06022894 (2000).
-
-
-
DelMar, E.G.1
Barmore, R.M.2
Sheehan, D.3
Van Wagenen, B.C.4
Callahan, J.F.5
Keenan, R.M.6
Kotecha, N.R.7
Lago, M.A.8
Southall, L.S.9
Thompson, M.10
-
48
-
-
0013401210
-
-
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
-
-
Heterocyclic compounds, useful as allosteric effectors at muscarinic receptors. WO-09603377 (1996)
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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).
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Birdsall, N.1
Lazareno, S.2
Naruto, S.3
Sugimoto, M.4
Koyama, K.5
Marumoto, S.6
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