-
3
-
-
0028177513
-
1c subtype
-
1c Subtype. Mol. Pharmacol. 1994, 45, 703-708.
-
(1994)
Mol. Pharmacol.
, vol.45
, pp. 703-708
-
-
Forray, C.1
Bard, J.A.2
Wetzel, J.M.3
Chiu, G.4
Shapiro, E.5
Tang, R.6
Lepor, H.7
Hartig, P.R.8
Weinshank, R.L.9
Branchek, T.A.10
Gluchowski, C.11
-
4
-
-
0029065459
-
2+ channel antagonist niguldipine
-
2+ Channel Antagonist Niguldipine. J. Med. Chem. 1995, 38, 1579-1581.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 1579-1581
-
-
Wetzel, J.M.1
Miao, S.W.2
Forray, C.3
Borden, L.A.4
Branchek, T.A.5
Gluchowski, C.6
-
5
-
-
15644366034
-
1a. Adrenoceptor-selective antagonist that inhibits phenylephrine-induced contraction of the human prostate
-
1a. Adrenoceptor-Selective Antagonist That Inhibits Phenylephrine-Induced Contraction of the Human Prostate. J. Med. Chem. 1998, 41, 2643-2650.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 2643-2650
-
-
Wong, W.C.1
Chiu, G.2
Wetzel, J.M.3
Marzabadi, M.R.4
Nagarathnam, D.5
Wang, D.6
Fang, J.7
Miao, S.W.8
Hong, X.9
Forray, C.10
Vaysse, P.J.-J.11
Branchek, T.A.12
Gluchowski, C.13
Tang, R.14
Lepor, H.15
-
6
-
-
0032542265
-
1a adrenoceptor selective dihydropyridine antagonists for the treatment of benign prostatic hyperplasia
-
1a Adrenoceptor Selective Dihydropyridine Antagonists for the Treatment of Benign Prostatic Hyperplasia. J. Med. Chem. 1998, 41, 5320-5333.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 5320-5333
-
-
Nagarathnam, D.1
Wetzel, J.M.2
Miao, S.W.3
Marzabadi, M.R.4
Chiu, G.5
Wong, W.C.6
Hong, X.7
Fang, J.8
Forray, C.9
Branchek, T.A.10
Heydorn, W.E.11
Chang, R.S.L.12
Broten, T.13
Schorn, T.W.14
Gluchowski, C.15
-
7
-
-
0344146598
-
1a adrenoceptor-selective antagonists. 1. Structure-activity relationships of dihydropyrimidinones
-
1a Adrenoceptor-Selective Antagonists. 1. Structure-Activity Relationships of Dihydropyrimidinones. J. Med. Chem. 1999, 42, 4764-4777.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 4764-4777
-
-
Nagarathnam, D.1
Miao, S.W.2
Chiu, G.3
Fang, J.4
Lagu, B.5
Murali Dhar, T.G.6
Zhang, J.7
Tyagarajan, S.8
Marzabadi, M.R.9
Zhang, F.10
Wong, W.C.11
Sun, W.12
Tian, D.13
Wetzel, J.M.14
Forray, C.15
Chang, R.S.L.16
Broten, T.P.17
Schorn, T.W.18
Chen, T.B.19
O'Malley, S.20
Ransom, R.21
Schneck, K.22
Bendesky, R.23
Harrell, C.M.24
Gluchowski, C.25
more..
-
8
-
-
0032749430
-
1a adrenoceptor-selective antagonists. 2. Approaches To eliminate opioid agonist metabolites via modification of linker and 4-methoxycarbonyl-4-phenylpiperidine moiety
-
1a Adrenoceptor-Selective Antagonists. 2. Approaches To Eliminate Opioid Agonist Metabolites via Modification of Linker and 4-Methoxycarbonyl-4-phenylpiperidine Moiety. J. Med. Chem. 1998, 42, 4778-4793.
-
(1998)
J. Med. Chem.
, vol.42
, pp. 4778-4793
-
-
Murali Dhar, T.G.1
Nagarathnam, D.2
Marzabadi, M.R.3
Lagu, B.4
Wong, W.C.5
Chiu, G.6
Tyagarajan, S.7
Miao, S.W.8
Zhang, J.9
Zhang, F.10
Sun, W.11
Tian, D.12
Shen, Q.13
Tang, C.14
Wetzel, J.M.15
Forray, C.16
Chang, R.S.L.17
Broten, T.P.18
Schorn, T.W.19
Chen, T.B.20
O'Malley, S.21
Ransom, R.22
Schneck, K.23
Bendesky, R.24
Harrell, C.M.25
Vyas, K.26
Zhang, K.27
Gilbert, J.28
Pettibone, D.J.29
Freidinger, R.30
Gluchowski, C.31
more..
-
9
-
-
0000940050
-
Synthesis of novel dihydropyrimidines and tetrahydropyrimidines
-
Cho, H.; Shima, K.; Hayashimatsu, M.; Ohnaka, Y.; Mizuno, A.; Takeuchi, Y. Synthesis of Novel Dihydropyrimidines and Tetrahydropyrimidines. J. Org. Chem. 1985, 50, 4227-4230.
-
(1985)
J. Org. Chem.
, vol.50
, pp. 4227-4230
-
-
Cho, H.1
Shima, K.2
Hayashimatsu, M.3
Ohnaka, Y.4
Mizuno, A.5
Takeuchi, Y.6
-
10
-
-
0000791751
-
An efficient synthesis of optically pure (S)-(-)-3-methylcyclohexanone
-
Thurkauf, A.; Hillery, P.; Jacobson, A. E.; Rice, K. C. An Efficient Synthesis of Optically Pure (S)-(-)-3-Methylcyclohexanone. J. Org. Chem. 1987, 52, 5466-5467.
-
(1987)
J. Org. Chem.
, vol.52
, pp. 5466-5467
-
-
Thurkauf, A.1
Hillery, P.2
Jacobson, A.E.3
Rice, K.C.4
-
11
-
-
0029738974
-
Inhibitors of human nitric oxide synthase isoforms with the carbamidine moiety as a common structural element
-
Moore, W. M.; Webber, R. K.; Fok, K. F.; Jerome, G. M.; Kornmeier, C. M.; Tjoeng, F. S.; Currie, M. G. Inhibitors of Human Nitric Oxide Synthase Isoforms with The Carbamidine Moiety as A Common Structural Element. Bioorg. Med. Chem. 1996, 4, 1559-1564.
-
(1996)
Bioorg. Med. Chem.
, vol.4
, pp. 1559-1564
-
-
Moore, W.M.1
Webber, R.K.2
Fok, K.F.3
Jerome, G.M.4
Kornmeier, C.M.5
Tjoeng, F.S.6
Currie, M.G.7
-
12
-
-
0005234353
-
-
Munson, P. L., Ed.; Chapman and Hall: New York
-
Smith, A. P.; Lee, N. M.; Loh, H. H. In Principles of Pharmacology; Munson, P. L., Ed.; Chapman and Hall: New York; pp 399-416.
-
Principles of Pharmacology
, pp. 399-416
-
-
Smith, A.P.1
Lee, N.M.2
Loh, H.H.3
-
13
-
-
0038653828
-
-
Merck & Co.: Rahway, NJ
-
The Merck Index; Budavari, S., Ed.; Merck & Co.: Rahway, NJ, 1989; p 5734.
-
(1989)
The Merck Index
, pp. 5734
-
-
Budavari, S.1
-
14
-
-
0032752508
-
1a adrenoceptor-selective antagonists. 3. Approaches to eliminate opioid agonist metabolites using phenylpiperazines in side chains
-
1a Adrenoceptor-Selective Antagonists. 3. Approaches To Eliminate Opioid Agonist Metabolites Using Phenylpiperazines in Side Chains. J. Med. Chem. 1999, 42, 4794-4803.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 4794-4803
-
-
Lagu, B.1
Tian, D.2
Nagarathnam, D.3
Marzabadi, M.R.4
Wong, W.C.5
Miao, S.W.6
Zhang, F.7
Sun, W.8
Chiu, G.9
Fang, J.10
Forray, C.11
Chang, R.S.L.12
Ransom, R.13
Zhang, K.14
Vyas, K.15
Gluchowski, C.16
-
15
-
-
0029555969
-
The specific contribution of the novel alpha-1D adrenoceptor to the contraction of vascular smooth muscle
-
Piascik, M. T.; Guarino, R. D.; Smith, M. S.; Soltis, E. E.; Saussy, S. S.; Perez, D. M. The Specific Contribution of the Novel alpha-1D Adrenoceptor to the Contraction of Vascular Smooth Muscle. J. Pharmacol. Exp. Ther. 1995, 275, 1583-1589.
-
(1995)
J. Pharmacol. Exp. Ther.
, vol.275
, pp. 1583-1589
-
-
Piascik, M.T.1
Guarino, R.D.2
Smith, M.S.3
Soltis, E.E.4
Saussy, S.S.5
Perez, D.M.6
-
16
-
-
0028981559
-
Characterization of an alpha-1D adrenoceptor mediating the contractile response of rat aorta to noradrenaline
-
Kenny, B. A.; Chalmers, D. H.; Philpott, P. C.; Naylor, A. M. Characterization of an Alpha-1D Adrenoceptor Mediating the Contractile Response of Rat Aorta to Noradrenaline. Br. J. Pharmacol. 1995, 115, 981-986.
-
(1995)
Br. J. Pharmacol.
, vol.115
, pp. 981-986
-
-
Kenny, B.A.1
Chalmers, D.H.2
Philpott, P.C.3
Naylor, A.M.4
-
17
-
-
0032571013
-
Alpha-1 adrenoceptor subtypes and two receptor systems in vascular tissues
-
J.
-
Muramatsu, I.; Murata, S.; Isaka, H.; Piao, L.; J.; Zhu, J.; Suzuki, F.; Miyamoto, S.; Oshita, M.; Watanabe, Y.; Tanigichi, T. Alpha-1 adrenoceptor subtypes and two receptor systems in vascular tissues. Life Sci. 1998, 62, 1461-1465.
-
(1998)
Life Sci.
, vol.62
, pp. 1461-1465
-
-
Muramatsu, I.1
Murata, S.2
Isaka, H.3
Piao, L.4
Zhu, J.5
Suzuki, F.6
Miyamoto, S.7
Oshita, M.8
Watanabe, Y.9
Tanigichi, T.10
-
18
-
-
0027970994
-
Pharmacological characterization of alpha-1A adrenoceptor subtypes in the human prostate: Functional and binding studies
-
Muramatsu, I.; Oshita, M.; Ohmura, T.; Kigoshi, S.; Akino, H.; Gobra, M.; Okada, K. Pharmacological Characterization of Alpha-1A Adrenoceptor Subtypes in the Human Prostate: Functional and Binding Studies. Br. J. Urol. 1994, 74, 572-578.
-
(1994)
Br. J. Urol.
, vol.74
, pp. 572-578
-
-
Muramatsu, I.1
Oshita, M.2
Ohmura, T.3
Kigoshi, S.4
Akino, H.5
Gobra, M.6
Okada, K.7
-
19
-
-
0030046789
-
RS-17053 (N-[2-(2-cyclopropylmethoxyphenoxy)-ethyl]-5-chloro-α,α-dimethyl-1h- indole-3-ethanamine hydrochloride), a selective alpha-1A adrenoceptor antagonist, displays low affinity for functionalalpha-1 adrenoceptors in human prostate: Implications for adrenoceptor classification
-
Ford, A. P.; Arredondo, N. F.; Blue, D. R. J.; Bonhaus, D. W.; Jasper, J.; Kava, M. S.; Lesnick, J.; Pfister, J. R.; Shieh, I. A.; Vimont, R. L.; Williams, T. J.; McNeal, J. E.; Stamey, T. A.; Clarke, D. E. RS-17053 (N-[2-(2-cyclopropylmethoxyphenoxy)-ethyl]-5-chloro-α,α-dimethyl-1H- indole-3-ethanamine hydrochloride), a Selective Alpha-1A Adrenoceptor Antagonist, Displays Low Affinity for FunctionalAlpha-1 Adrenoceptors in Human Prostate: Implications for Adrenoceptor Classification. Mol. Pharmacol. 1996, 49, 209-215.
-
(1996)
Mol. Pharmacol.
, vol.49
, pp. 209-215
-
-
Ford, A.P.1
Arredondo, N.F.2
Blue, D.R.J.3
Bonhaus, D.W.4
Jasper, J.5
Kava, M.S.6
Lesnick, J.7
Pfister, J.R.8
Shieh, I.A.9
Vimont, R.L.10
Williams, T.J.11
McNeal, J.E.12
Stamey, T.A.13
Clarke, D.E.14
-
20
-
-
0032589082
-
Human cloned alpha1A-adrenoceptor isoforms display alphalL-adrenoceptor pharmacology in functional studies
-
Daniels, D. V.; Gever, J. R.; Jasper, J. R.; Kava, M. S.; Lesnick, J. D.; Melloy, T. D.; Stephan, G.; Williams, T. J.; Clarke, D. E.; Chang, D. J.; Ford, A. P. Human cloned alpha1A-adrenoceptor isoforms display alphalL-adrenoceptor pharmacology in functional studies. Eur. J. Pharmacol. 1999, 370, 337-343.
-
(1999)
Eur. J. Pharmacol.
, vol.370
, pp. 337-343
-
-
Daniels, D.V.1
Gever, J.R.2
Jasper, J.R.3
Kava, M.S.4
Lesnick, J.D.5
Melloy, T.D.6
Stephan, G.7
Williams, T.J.8
Clarke, D.E.9
Chang, D.J.10
Ford, A.P.11
|