-
1
-
-
0024470363
-
3-adrenergic receptor
-
3-adrenergic receptor. Science. 1989, 245, 1118-1121.
-
(1989)
Science
, vol.245
, pp. 1118-1121
-
-
Emorine, L.J.1
Marullo, S.2
Briend-Sutren, M.-M.3
Patey, G.4
Tate, K.5
Delavier-Klutchko, C.6
Strosberg, A.D.7
-
2
-
-
0020557241
-
Thermogenic and antiobesity activity of a novel β-adrenoceptor agonist (BRL 26830A) in mice and rats
-
(a) Arch, J. R. S.; Ainsworth, A. T. Thermogenic and antiobesity activity of a novel β-adrenoceptor agonist (BRL 26830A) in mice and rats. Am. J. Clin. Nutr. 1983, 38, 549-558.
-
(1983)
Am. J. Clin. Nutr
, vol.38
, pp. 549-558
-
-
Arch, J.R.S.1
Ainsworth, A.T.2
-
3
-
-
0021363316
-
Atypical β-adrenoceptors on brown adpocytes as target for anti-obesity drugs
-
(b) Arch, J. R.; Ainsworth, A. T.; Cawthorne, M. A.; Piercy, V.; Sennitt, M. V.; Thod, V. E.; Wilson, C.; Wilson, S. Atypical β-adrenoceptors on brown adpocytes as target for anti-obesity drugs. Nature 1983, 309, 163-165.
-
(1983)
Nature
, vol.309
, pp. 163-165
-
-
Arch, J.R.1
Ainsworth, A.T.2
Cawthorne, M.A.3
Piercy, V.4
Sennitt, M.V.5
Thod, V.E.6
Wilson, C.7
Wilson, S.8
-
4
-
-
0031711501
-
3-adrenoceptor-mediated relaxation of the human detrusor
-
3-adrenoceptor-mediated relaxation of the human detrusor. Acta Physiol. Scand. 1998, 164, 117-118.
-
(1998)
Acta Physiol. Scand
, vol.164
, pp. 117-118
-
-
Igawa, Y.1
Yamazaki, Y.2
Takeda, H.3
Akahane, M.4
Ajisawa, Y.5
Yoneyama, T.6
Nishizawa, O.7
-
5
-
-
0032983692
-
3- adrenoceptor in the human detrusor muscle
-
3- adrenoceptor in the human detrusor muscle. Br. J. Pharmacol. 1999, 126, 819-825.
-
(1999)
Br. J. Pharmacol
, vol.126
, pp. 819-825
-
-
Igawa, Y.1
Yamazaki, Y.2
Takeda, H.3
Hayakawa, K.4
Akahane, M.5
Ajisawa, Y.6
Yoneyama, T.7
Nishizawa, O.8
Anderrson, K.-E.9
-
6
-
-
0032588710
-
3- adrenoceptor subtypes in relaxation of the human urinary bladder detrusor: Analysis by molecular biological and pharmacological methods
-
3- adrenoceptor subtypes in relaxation of the human urinary bladder detrusor: analysis by molecular biological and pharmacological methods. J. Pharmacol. Exp. Ther. 1999, 288, 1367-1373.
-
(1999)
J. Pharmacol. Exp. Ther
, vol.288
, pp. 1367-1373
-
-
Takeda, M.1
Obara, K.2
Mizusawa, T.3
Tomita, Y.4
Arai, K.5
Tsutsui, T.6
Hatano, A.7
Takahashi, K.8
Nomura, S.9
-
7
-
-
0033074328
-
3-adrenoceptor in human and rat detrusor muscle
-
3-adrenoceptor in human and rat detrusor muscle. J. Urol. 1999, 16, 680-685.
-
(1999)
J. Urol
, vol.16
, pp. 680-685
-
-
Fujimura, T.1
Tamura, K.2
Tsutsumi, T.3
Yamamoto, T.4
Nakamura, K.5
Koibuchi, Y.6
Kobayashi, M.7
Ymaguchi, O.8
-
8
-
-
0036011136
-
3-adrenoceptors in human detrusor muscle
-
3-adrenoceptors in human detrusor muscle. Urology 2002, 59 (Suppl 5A), 25-29.
-
(2002)
Urology
, vol.59
, Issue.SUPPL. 5A
, pp. 25-29
-
-
Yamaguchi, O.1
-
9
-
-
23644445651
-
Involvement of cyclic AMP-dependent and -independent mechanisms in the relaxation of rat detrusor muscle via β-adrenoceptors
-
(c) Uchida, H.; Shishido, K.; Nomiya, M.; Yamaguchi, O. Involvement of cyclic AMP-dependent and -independent mechanisms in the relaxation of rat detrusor muscle via β-adrenoceptors. Eur. J. Pharmacol. 2005, 518, 195-202.
-
(2005)
Eur. J. Pharmacol
, vol.518
, pp. 195-202
-
-
Uchida, H.1
Shishido, K.2
Nomiya, M.3
Yamaguchi, O.4
-
10
-
-
33750633989
-
3-adrenoceptor selective agonist, on relaxation of the human detrusor muscle in vitro
-
3-adrenoceptor selective agonist, on relaxation of the human detrusor muscle in vitro. Neurourol. Urodyn. 2006, 25, 815-819.
-
(2006)
Neurourol. Urodyn
, vol.25
, pp. 815-819
-
-
Yamanishi, T.1
Yasuda, K.2
Kitahara, S.3
Nakai, H.4
Yoshida, K.5
Iizuka, H.6
-
11
-
-
33749036297
-
3-adrenoceptor agonist to treat the overactive bladder
-
3-adrenoceptor agonist to treat the overactive bladder. Urol. Clin. N. Am. 2006, 33 (4), 539-543.
-
(2006)
Urol. Clin. N. Am
, vol.33
, Issue.4
, pp. 539-543
-
-
Furuta, A.1
Thomas, C.O.2
Higaki, M.3
Chancellor, M.O.4
Yoshimura, N.5
Yamaguchi, O.6
-
12
-
-
0037413237
-
3-adrenoceptor agonistic activity of 4′-hydroxynorephedrine derivative as an agent for treatment of frequent urination and urinary incontinence
-
3-adrenoceptor agonistic activity of 4′-hydroxynorephedrine derivative as an agent for treatment of frequent urination and urinary incontinence. J. Med. Chem. 2003, 46, 105-112.
-
(2003)
J. Med. Chem
, vol.46
, pp. 105-112
-
-
Tanaka, N.1
Tamai, T.2
Mukaiyama, H.3
Hirabayashi, A.4
Muranaka, H.5
Ishikawa, T.6
Kobayashi, J.7
Akahane, S.8
Akahane, M.9
-
13
-
-
0034858180
-
3-Adrenoceptor agonists as anti-diabetic and anti-obesity drugs in humans
-
3-Adrenoceptor agonists as anti-diabetic and anti-obesity drugs in humans. Curr. Pharm. Des. 2001, 7, 1433.
-
(2001)
Curr. Pharm. Des
, vol.7
, pp. 1433
-
-
de Souza, C.J.1
Burkey, B.F.2
-
15
-
-
41149089082
-
-
Shuker, A. J.; Bell, M. G.; Bloomquist, W.; Calligaro, D. O.; Cohen, M. L.; Crowell, T. A.; Cusick, T. S.; Drost, C. A.; Evrard, D. A.; Hahn, P. J.; Heiman, M. L.; Jesudason, C. D.; Jones, C. D.; Kim, G.; Kriaucinus, A. V.; Matthews, D. P.; McDonald, J. H.; Neel, D. A.; Palkowitz, A. D.; Peters, M. K.; Rito, C. J.; Siegel, M. G.; Stephens, T. W.; Winter, M. A.; Dananberg, J. 217th ACS National Meeting, Anaheim, CA, U.S.A., 1999,MEDI-159.
-
Shuker, A. J.; Bell, M. G.; Bloomquist, W.; Calligaro, D. O.; Cohen, M. L.; Crowell, T. A.; Cusick, T. S.; Drost, C. A.; Evrard, D. A.; Hahn, P. J.; Heiman, M. L.; Jesudason, C. D.; Jones, C. D.; Kim, G.; Kriaucinus, A. V.; Matthews, D. P.; McDonald, J. H.; Neel, D. A.; Palkowitz, A. D.; Peters, M. K.; Rito, C. J.; Siegel, M. G.; Stephens, T. W.; Winter, M. A.; Dananberg, J. 217th ACS National Meeting, Anaheim, CA, U.S.A., 1999,MEDI-159.
-
-
-
-
16
-
-
0034687253
-
-
3 adrenergic receptor agonist, (R)-N-[4-[2-[[2- hydroxy-2-(3-pyridinyl)ethyl]amino]ethyl]phenyl]-4-[4-[4-(trifluoromethyl) phenyl]thiazol-2-yl]benzenesulfonamide. J. Med. Chem. 2000, 43, 3832-3836.
-
3 adrenergic receptor agonist, (R)-N-[4-[2-[[2- hydroxy-2-(3-pyridinyl)ethyl]amino]ethyl]phenyl]-4-[4-[4-(trifluoromethyl) phenyl]thiazol-2-yl]benzenesulfonamide. J. Med. Chem. 2000, 43, 3832-3836.
-
-
-
-
17
-
-
33646457171
-
3-adrenergic receptor agonists
-
3-adrenergic receptor agonists. J. Med. Chem. 2006, 49, 2758-2771.
-
(2006)
J. Med. Chem
, vol.49
, pp. 2758-2771
-
-
Uehling, D.E.1
Shearer, B.G.2
Donaldson, K.H.3
Chao, E.Y.4
Deaton, D.N.5
Adkison, K.K.6
Brown, K.K.7
Cariello, N.F.8
Faison, W.L.9
Lancaster, M.E.10
Lin, J.11
Hart, R.12
Milliken, T.O.13
Paulik, M.A.14
Sherman, B.W.15
Sugg, E.E.16
Cowan, C.17
-
18
-
-
34447336958
-
3-adrenergic receptor agonists containing heterobiaryl carboxylic acids
-
3-adrenergic receptor agonists containing heterobiaryl carboxylic acids. Bioorg. Med. Chem. Lett. 2007, 17, 4670-4677.
-
(2007)
Bioorg. Med. Chem. Lett
, vol.17
, pp. 4670-4677
-
-
Shearer, B.G.1
Chao, E.Y.2
Uehling, D.E.3
Deaton, D.N.4
Cowan, C.5
Sherman, B.W.6
Milliken, T.7
Faison, W.8
Brown, K.9
Adkison, K.K.10
Lee, F.11
-
19
-
-
0038071650
-
3- adrenergic receptor agonists as potential therapeutic agents for obesity and type-II diabetes
-
3- adrenergic receptor agonists as potential therapeutic agents for obesity and type-II diabetes. Prog. Med. Chem. 2003, 41, 167-189.
-
(2003)
Prog. Med. Chem
, vol.41
, pp. 167-189
-
-
Hu, B.1
Jennings, L.L.2
-
21
-
-
0030950052
-
3 binding selectivity
-
3 binding selectivity. Bioorg. Med. Chem. Lett. 1997, 7, 1583-1588.
-
(1997)
Bioorg. Med. Chem. Lett
, vol.7
, pp. 1583-1588
-
-
Sher, P.M.1
Mathur, A.2
Fisher, L.G.3
Wu, G.4
Skwish, S.5
Michel, I.M.6
Seiler, S.M.7
Dickinson, K.E.8
-
22
-
-
0034546069
-
3 adrenergic receptor
-
3 adrenergic receptor. Med. Chem. Res. 2000, 10, 164-177.
-
(2000)
Med. Chem. Res
, vol.10
, pp. 164-177
-
-
Malamas, M.S.1
Largis, E.2
Gunawan, I.3
Li, Z.4
Tillett, J.5
Han, S.C.-H.6
Mulvey, R.7
-
23
-
-
0037203971
-
3 adrenergic receptor agonists containing acylsulfonamide, sulfonyl-sulfonamide, and sulfonylurea carboxylic acid isosteres
-
3 adrenergic receptor agonists containing acylsulfonamide, sulfonyl-sulfonamide, and sulfonylurea carboxylic acid isosteres. J. Med. Chem. 2002, 45, 567-583.
-
(2002)
J. Med. Chem
, vol.45
, pp. 567-583
-
-
Uehling, D.E.1
Donaldson, K.H.2
Deaton, D.N.3
Hyman, C.E.4
Sugg, E.E.5
Barrett, D.G.6
Hughes, R.G.7
Reitter, B.8
Adkison, K.K.9
Lancaster, M.E.10
Lee, F.11
Hart, R.12
Paulik, M.A.13
Sherman, B.W.14
True, T.15
Cowan, C.16
-
24
-
-
0033543625
-
3 adrenergic receptor agonist
-
3 adrenergic receptor agonist. Tetrahedron Lett. 1999, 40, 6739.
-
(1999)
Tetrahedron Lett
, vol.40
, pp. 6739
-
-
Chung, Y.L.J.1
Ho, G.J.2
Chartrain, M.3
Roberge, C.4
Zhao, D.5
Leazer, J.6
Farr, R.7
Robbins, M.8
Emerson, K.9
Mathre, D.J.10
McNamara, J.M.11
Hughes, D.L.12
Grabowski, J.E.13
Reider, P.J.14
-
25
-
-
0028304844
-
Two efficient methods for the cleavage of pinanediol boronate esters yielding the free boronic acids
-
Coutts, S. J.; Adams, J.; Krolikowski, D.; Snow, R. J. Two efficient methods for the cleavage of pinanediol boronate esters yielding the free boronic acids. Tetrahedron Lett. 1994, 35, 5109.
-
(1994)
Tetrahedron Lett
, vol.35
, pp. 5109
-
-
Coutts, S.J.1
Adams, J.2
Krolikowski, D.3
Snow, R.J.4
-
26
-
-
0032492942
-
New N- and O-arylations with phenylboronic acids and cupric acetate
-
(a) Chan, D. M. T.; Monaco, K. L.; Wang, R.-P.; Winters, M. P. New N- and O-arylations with phenylboronic acids and cupric acetate. Tetrahedron Lett. 1998, 39, 2933-2936.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 2933-2936
-
-
Chan, D.M.T.1
Monaco, K.L.2
Wang, R.-P.3
Winters, M.P.4
-
27
-
-
0032492980
-
Synthesis of diaryl ethers through the copper-promoted arylation of phenols with arylboronic acids. An expedient synthesis of thyroxine
-
(b) Evans, D. A.; Katz, J. L.; West, T. R. Synthesis of diaryl ethers through the copper-promoted arylation of phenols with arylboronic acids. An expedient synthesis of thyroxine. Tetrahedron Lett. 1998, 39, 2937-2940.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 2937-2940
-
-
Evans, D.A.1
Katz, J.L.2
West, T.R.3
-
28
-
-
0035810387
-
Intramolecular O-arylation of phenols with phenylboronic acids: Application to the synthesis of macrocyclic metalloproteinase inhibitors
-
(c) Decicco, C. P.; Song, Y.; Evans, D. A. Intramolecular O-arylation of phenols with phenylboronic acids: application to the synthesis of macrocyclic metalloproteinase inhibitors. Org. Lett. 2001, 3, 1029-1032.
-
(2001)
Org. Lett
, vol.3
, pp. 1029-1032
-
-
Decicco, C.P.1
Song, Y.2
Evans, D.A.3
-
29
-
-
41149171519
-
-
3 adrenergic receptor agonists, WO2004002939, 2004.
-
3 adrenergic receptor agonists, WO2004002939, 2004.
-
-
-
-
30
-
-
0002222783
-
Synthesis of 4-(4′-hydroxythiophenyl) phenylethylamine. (Thiotyronamine) and its lower homolog
-
(b) Petit, L.; Sonnier, M. Synthesis of 4-(4′-hydroxythiophenyl) phenylethylamine. (Thiotyronamine) and its lower homolog. Bull. Soc. Chim. Fr. 1974, 477-478.
-
(1974)
Bull. Soc. Chim. Fr
, pp. 477-478
-
-
Petit, L.1
Sonnier, M.2
-
31
-
-
41149084329
-
-
A dosing solution containing 8b, 8c, 8d, and 8a was prepared in PEG400, and the dose of each compound was 1.0 mg/kg. After administration of the dosing solution to male rats, dogs, and monkeys, the blood was collected and centrifuged to separate plasma. The plasma samples were analyzed by LC/MS/MS for determination of plasma concentrations of 8b, 8c, 8d, and 8a.
-
(a) A dosing solution containing 8b, 8c, 8d, and 8a was prepared in PEG400, and the dose of each compound was 1.0 mg/kg. After administration of the dosing solution to male rats, dogs, and monkeys, the blood was collected and centrifuged to separate plasma. The plasma samples were analyzed by LC/MS/MS for determination of plasma concentrations of 8b, 8c, 8d, and 8a.
-
-
-
-
32
-
-
33746206240
-
Metabolism investigation leading to novel drug design 2: Orally active prostacyclin mimetics. Part 5
-
(b) Takamura, F.; Tanaka, A.; Takasugi, H.; Taniguchi, K.; Nishio, M.; Seki, J.; Hattori, K. Metabolism investigation leading to novel drug design 2: Orally active prostacyclin mimetics. Part 5. Bioorg. Med Chem. Lett. 2006, 16, 4475-4478.
-
(2006)
Bioorg. Med Chem. Lett
, vol.16
, pp. 4475-4478
-
-
Takamura, F.1
Tanaka, A.2
Takasugi, H.3
Taniguchi, K.4
Nishio, M.5
Seki, J.6
Hattori, K.7
-
33
-
-
0036238280
-
A comparative study of artificial membrane permeability assay for high throughput profiling of drug absorption potential
-
Zhu, C.; Jiang, L.; Chen, T. M.; Hwang, K. K. A comparative study of artificial membrane permeability assay for high throughput profiling of drug absorption potential. Eur. J. Med. Chem. 2002, 37, 399-407.
-
(2002)
Eur. J. Med. Chem
, vol.37
, pp. 399-407
-
-
Zhu, C.1
Jiang, L.2
Chen, T.M.3
Hwang, K.K.4
-
34
-
-
41149109888
-
-
Hurnaus, R.; Reiffen, M.; Sauter, R.; Grell, W.; Rupprecht, E. Preparation of new phenylethanolamines and pharmaceuticals containing them, WO9006299, 1990.
-
Hurnaus, R.; Reiffen, M.; Sauter, R.; Grell, W.; Rupprecht, E. Preparation of new phenylethanolamines and pharmaceuticals containing them, WO9006299, 1990.
-
-
-
-
35
-
-
41149142711
-
-
Measurements of the concentration of 10a, 10e, and 4 (FK175) in plasma were measured using HPLC or LC/MS.
-
Measurements of the concentration of 10a, 10e, and 4 (FK175) in plasma were measured using HPLC or LC/MS.
-
-
-
|