-
1
-
-
0020587209
-
-
1. Arrang, J.-M.; Garbarg, M.; Schwartz, J.-C. Nature (London) 1983, 302, 832.
-
(1983)
Nature (London)
, vol.302
, pp. 832
-
-
Arrang, J.-M.1
Garbarg, M.2
Schwartz, J.-C.3
-
2
-
-
0023653116
-
-
2. Arrang, J.-M.; Garbarg, M.; Lancelot, J.-C.; Lecomte J.-M.; Pollard, H.; Robba, M.; Schunack, W.; Schwanz, J.-C. Nature (London) 1987, 327, 117.
-
(1987)
Nature (London)
, vol.327
, pp. 117
-
-
Arrang, J.-M.1
Garbarg, M.2
Lancelot, J.-C.3
Lecomte, J.-M.4
Pollard, H.5
Robba, M.6
Schunack, W.7
Schwanz, J.-C.8
-
3
-
-
0025319293
-
-
3. Schwartz, J.-C.; Arrang, J.-M.; Garbarg, M.; Pollard, H. A. Agents Actions 1990, 30, 13.
-
(1990)
Agents Actions
, vol.30
, pp. 13
-
-
Schwartz, J.-C.1
Arrang, J.-M.2
Garbarg, M.3
Pollard, H.A.4
-
4
-
-
0021852055
-
-
4. Arrang, J.-M.; Garbarg, M.; Schwartz, J.-C. Neuroscience 1985, 17, 553.
-
(1985)
Neuroscience
, vol.17
, pp. 553
-
-
Arrang, J.-M.1
Garbarg, M.2
Schwartz, J.-C.3
-
5
-
-
0023639903
-
-
5. Arrang, J.-M.; Garbarg, M.; Schwartz, J.-C. Neuroscience 1987, 23, 149.
-
(1987)
Neuroscience
, vol.23
, pp. 149
-
-
Arrang, J.-M.1
Garbarg, M.2
Schwartz, J.-C.3
-
6
-
-
0023821071
-
-
6. Schlicker, E., Betz, R., Gothert, M. Naunyn-Schmied. Arch. Pharmacol. 1988, 337, 588.
-
(1988)
Naunyn-Schmied. Arch. Pharmacol.
, vol.337
, pp. 588
-
-
Schlicker, E.1
Betz, R.2
Gothert, M.3
-
7
-
-
0010544771
-
-
7. Schlicker, E., Betz, R., Gothert, M. Naunyn-Schmied. Arch. Pharmacol. 1990, 324, 497.
-
(1990)
Naunyn-Schmied. Arch. Pharmacol.
, vol.324
, pp. 497
-
-
Schlicker, E.1
Betz, R.2
Gothert, M.3
-
8
-
-
0026614109
-
-
8. Clapham, J., Kilpatrick, G. J., Br. J. Pharmacol. 1992, 107, 919.
-
(1992)
Br. J. Pharmacol.
, vol.107
, pp. 919
-
-
Clapham, J.1
Kilpatrick, G.J.2
-
9
-
-
0026574910
-
-
9. Hey, J. A.; del Prado, M; Egan, R. W.; Kreutner, W.; Chapman, R. Eur. J. Pharmacol. 1992, 277, 421.
-
(1992)
Eur. J. Pharmacol.
, vol.277
, pp. 421
-
-
Hey, J.A.1
Del Prado, M.2
Egan, R.W.3
Kreutner, W.4
Chapman, R.5
-
10
-
-
0029062904
-
-
10. Shih, N.-Y.; Lupo, Jr. A. T.; Aslanian, R.; Orlando, S.; Piwinski, J. J.; Green, M. J.; Ganguly A. K.; Clark, M. A.; Tozzi, S.; Kreutner, W.; Hey, J. A. J. Med. Chem. 1995, 38, 1593.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 1593
-
-
Shih, N.-Y.1
Lupo A.T., Jr.2
Aslanian, R.3
Orlando, S.4
Piwinski, J.J.5
Green, M.J.6
Ganguly, A.K.7
Clark, M.A.8
Tozzi, S.9
Kreutner, W.10
Hey, J.A.11
-
12
-
-
0010612243
-
-
note
-
1-mediated bronchospasm (in vivo); see ref 9.
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-
-
-
13
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0010575163
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-
note
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1-mediated bronchoconstrictor effect at doses ≥ 0.3 mg/kg, iv. Compound 8 produced significant bronchoconstrictor effects at a dose of 0.3 mg/kg, iv.
-
-
-
-
14
-
-
0022273542
-
-
13. Arrang, J.-M.; Schwartz, J.-C.; Schunack, W. Eur. J. Pharmacol. 1985, 117, 109.
-
(1985)
Eur. J. Pharmacol.
, vol.117
, pp. 109
-
-
Arrang, J.-M.1
Schwartz, J.-C.2
Schunack, W.3
-
15
-
-
0010577577
-
-
note
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14. Resolutions (≥ 99% ee) were accomplished via chiral stationary phase HPLC of the di-t-BOC derivatives of (±)-3a. Absolute stereochemistry of the enantiomers of 3a were assigned based upon a single crystal X-ray analysis of the hydrocholide salt of (+)-3a.
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-
16
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0010576193
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-
3-antagonists. The assay used is based on studies described previously: Trzeciakowski; see Trzeciakowski, J. P. J. Pharmacol. Exp. Ther. 1987, 243, 84.
-
(1987)
J. Pharmacol. Exp. Ther.
, vol.243
, pp. 84
-
-
Trzeciakowski, J.P.1
-
17
-
-
0026699752
-
-
3-agonist activity was determined in vivo using a model previously described: Hey, J. A.; del Prado, M.; Egan, R. W.; Kreutner, W.; Chapman, R. W. Br. J. Pharmacol. 1992, 107, 347.
-
(1992)
Br. J. Pharmacol.
, vol.107
, pp. 347
-
-
Hey, J.A.1
Del Prado, M.2
Egan, R.W.3
Kreutner, W.4
Chapman, R.W.5
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