-
1
-
-
0020465411
-
Lithium amplifies agonist dependent phosphatidylinositol responses in brain and salivary glands
-
Berridge, M.J., Downes, C.P., Hanley, M.R., 1982. Lithium amplifies agonist dependent phosphatidylinositol responses in brain and salivary glands. Biochem. J. 206, 587-596.
-
(1982)
Biochem. J.
, vol.206
, pp. 587-596
-
-
Berridge, M.J.1
Downes, C.P.2
Hanley, M.R.3
-
2
-
-
0027381126
-
Anti-emetic profile of a non-peptide neurokinin NK1 antagonist, CP 99,994 in ferrets
-
Bountra, C., Bunce, K., Dale, T., Gardner, C., Jordan, C., Twissell, D., Ward, P., 1993. Anti-emetic profile of a non-peptide neurokinin NK1 antagonist, CP 99,994 in ferrets. Eur. J. Pharmacol. 249, R3-R4.
-
(1993)
Eur. J. Pharmacol.
, vol.249
-
-
Bountra, C.1
Bunce, K.2
Dale, T.3
Gardner, C.4
Jordan, C.5
Twissell, D.6
Ward, P.7
-
3
-
-
0027065565
-
Characterization of the binding of a potent, selective, radioiodinated antagonist to the human neurokinin-1 receptor
-
Cascieri, M.A., Ber, E., Fong, T.M., Sadowski, S., Bansal, A., Swain, C., Seward, E., Frances, B., Burns, D., Strader, C.D., 1992. Characterization of the binding of a potent, selective, radioiodinated antagonist to the human neurokinin-1 receptor. Mol. Pharmacol. 42, 458-463.
-
(1992)
Mol. Pharmacol.
, vol.42
, pp. 458-463
-
-
Cascieri, M.A.1
Ber, E.2
Fong, T.M.3
Sadowski, S.4
Bansal, A.5
Swain, C.6
Seward, E.7
Frances, B.8
Burns, D.9
Strader, C.D.10
-
4
-
-
0028318167
-
Characterization of the interaction of N-acyl-L-tryptophan benzyl ester neurokinin antagonists with the human neurokinin-1 receptor
-
Cascieri, M.A., Macleod, A.M., Underwood, D., Shiao, L.-L., Ber, E., Sadowski, S., Yu, H., Merchant, K.J., Swain, C.J., Strader, C.D., Fong, T.M., 1994. Characterization of the interaction of N-acyl-L-tryptophan benzyl ester neurokinin antagonists with the human neurokinin-1 receptor. J. Biol. Chem. 269, 2728-2732.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 2728-2732
-
-
Cascieri, M.A.1
Macleod, A.M.2
Underwood, D.3
Shiao, L.-L.4
Ber, E.5
Sadowski, S.6
Yu, H.7
Merchant, K.J.8
Swain, C.J.9
Strader, C.D.10
Fong, T.M.11
-
5
-
-
0029093852
-
Molecular characterization of a common binding site for small molecules within the transmembrane domain of G-protein coupled receptors
-
Cascieri, M.A., Fong, M.A., Strader, C.D., 1995a. Molecular characterization of a common binding site for small molecules within the transmembrane domain of G-protein coupled receptors. J. Pharmacol. Toxicol. Methods 33, 179-185.
-
(1995)
J. Pharmacol. Toxicol. Methods
, vol.33
, pp. 179-185
-
-
Cascieri, M.A.1
Fong, M.A.2
Strader, C.D.3
-
6
-
-
0028923493
-
Characterization of the interaction of diacylpiperazine antagonists with the human neurokinin-1 receptor: Identification of a common binding site for structurally dissimilar antagonists
-
Cascieri, M.A., Shiao, L.-L., Mills, S.G., MacCoss, M., Swain, C.J., Yu, H., Ber, E., Sadowski, S., Wu, M.T., Strader, C.D., Fong, T.M., 1995b. Characterization of the interaction of diacylpiperazine antagonists with the human neurokinin-1 receptor: identification of a common binding site for structurally dissimilar antagonists. Mol. Pharmacol. 47, 660-665.
-
(1995)
Mol. Pharmacol.
, vol.47
, pp. 660-665
-
-
Cascieri, M.A.1
Shiao, L.-L.2
Mills, S.G.3
MacCoss, M.4
Swain, C.J.5
Yu, H.6
Ber, E.7
Sadowski, S.8
Wu, M.T.9
Strader, C.D.10
Fong, T.M.11
-
8
-
-
0027402090
-
Amino-aromatic interaction between histidine 197 of the neurokinin-1 receptor and CP-96,345
-
Fong, T.M., Cascieri, M.A., Yu, H., Bansal, A., Swain, C., Strader, C.D., 1993. Amino-aromatic interaction between histidine 197 of the neurokinin-1 receptor and CP-96,345. Nature 362, 350-353.
-
(1993)
Nature
, vol.362
, pp. 350-353
-
-
Fong, T.M.1
Cascieri, M.A.2
Yu, H.3
Bansal, A.4
Swain, C.5
Strader, C.D.6
-
9
-
-
0028145295
-
The role of histidine 265 in antagonist binding to the neurokinin-1 receptor
-
Fong, T.M., Yu, H., Cascieri, M.A., Underwood, D., Swain, C.J., Strader, C.D., 1994a. The role of histidine 265 in antagonist binding to the neurokinin-1 receptor. J. Biol. Chem. 269, 2728-2732.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 2728-2732
-
-
Fong, T.M.1
Yu, H.2
Cascieri, M.A.3
Underwood, D.4
Swain, C.J.5
Strader, C.D.6
-
10
-
-
0028244827
-
Interaction of glutamine 165 in the fourth transmembrane domain of the human neurokinin-1 receptor with quinuclidine antagonists
-
Fong, T.M., Yu, H., Cascieri, M.A., Underwood, D., Swain, C.J., Strader, C.D., 1994b. Interaction of glutamine 165 in the fourth transmembrane domain of the human neurokinin-1 receptor with quinuclidine antagonists. J. Biol. Chem. 269, 14957-14961.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 14957-14961
-
-
Fong, T.M.1
Yu, H.2
Cascieri, M.A.3
Underwood, D.4
Swain, C.J.5
Strader, C.D.6
-
11
-
-
0029878786
-
2(S)-((3,5-bis(trifluoromethyl)benzyl)oxy)-3(S)-phenyl-4-((3-oxo-1,2,4- triazol-5-yl)methyl)-morpholine (1): A potent, orally active, morpholine-based human NK-1 receptor antagonist
-
Hale, J.J., Mills, S.G., MacCoss, M., Shah, S., Qi, H., Mathre, D.J., Cascieri, M.A., Sadowski, S., Strader, C.D., Pivnichny, J.V., MacIntyre, D.E., Metzger, J.M., 1996. 2(S)-((3,5-bis(trifluoromethyl)benzyl)oxy)-3(S)-phenyl-4-((3-oxo-1,2,4-triazol- 5-yl)methyl)-morpholine (1): a potent, orally active, morpholine-based human NK-1 receptor antagonist. J. Med. Chem. 39, 1760-1762.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 1760-1762
-
-
Hale, J.J.1
Mills, S.G.2
MacCoss, M.3
Shah, S.4
Qi, H.5
Mathre, D.J.6
Cascieri, M.A.7
Sadowski, S.8
Strader, C.D.9
Pivnichny, J.V.10
MacIntyre, D.E.11
Metzger, J.M.12
-
12
-
-
0028821240
-
Piperidine-ether based NK-1 antagonists 2: Investigation of the effect of N-substitution
-
Harrison, T., Owens, A.P., Williams, B.J., Swain, C.J., Baker, R., Hutson, P.H., Sadowski, S., Cascieri, M.A., 1995. Piperidine-ether based NK-1 antagonists 2: investigation of the effect of N-substitution. Biorg. Med. Chem. Lett. 5, 209-212.
-
(1995)
Biorg. Med. Chem. Lett.
, vol.5
, pp. 209-212
-
-
Harrison, T.1
Owens, A.P.2
Williams, B.J.3
Swain, C.J.4
Baker, R.5
Hutson, P.H.6
Sadowski, S.7
Cascieri, M.A.8
-
13
-
-
8944260413
-
1 antagonists
-
1 antagonists. J. Med. Chem. 39, 2907-2914.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 2907-2914
-
-
Ladduwahetty, T.1
Baker, R.2
Cascieri, M.A.3
Chambers, M.S.4
Haworth, K.5
Keown, L.6
MacIntyre, D.E.7
Metzger, J.M.8
Owen, S.9
Rycroft, W.10
Sadowski, S.11
Seward, E.M.12
Shepheard, S.13
Swain, C.J.14
Tattersail, F.D.15
Williamson, D.16
Hargreaves, R.J.17
-
14
-
-
0027175055
-
Effect of RP 67,580, a non-peptide neurokinin 1 receptor antagonist, on facilitation of a nociceptive spinal flexion reflex in the rat
-
Laird, J.M.A., Hargreaves, R.J., Hill, R.G., 1993. Effect of RP 67,580, a non-peptide neurokinin 1 receptor antagonist, on facilitation of a nociceptive spinal flexion reflex in the rat. Br. J. Pharmacol. 109, 713-718.
-
(1993)
Br. J. Pharmacol.
, vol.109
, pp. 713-718
-
-
Laird, J.M.A.1
Hargreaves, R.J.2
Hill, R.G.3
-
15
-
-
0028125669
-
Expression and solubilization of a recombinant human neurokinin-1 receptor in insect cells
-
Mazina, K.E., Strader, C.D., Fong, T.M., 1994. Expression and solubilization of a recombinant human neurokinin-1 receptor in insect cells. J. Recept. Res. 14, 63-73.
-
(1994)
J. Recept. Res.
, vol.14
, pp. 63-73
-
-
Mazina, K.E.1
Strader, C.D.2
Fong, T.M.3
-
16
-
-
0029017394
-
1,2,3-Trisubstituted cyclohexyl substance P antagonists: Significance of the ring nitrogen in piperidine-based NK-1 receptor antagonists
-
Mills, S.G., MacCoss, M., Underwood, D., Shah, S.K., Finke, P.E., Miller, D.J., Budha, R.J., Cascieri, M.A., Sadowski, S., Strader, C.D., 1995. 1,2,3-Trisubstituted cyclohexyl substance P antagonists: significance of the ring nitrogen in piperidine-based NK-1 receptor antagonists. Biorg. Med. Chem. Lett. 5, 1345-1350.
-
(1995)
Biorg. Med. Chem. Lett.
, vol.5
, pp. 1345-1350
-
-
Mills, S.G.1
MacCoss, M.2
Underwood, D.3
Shah, S.K.4
Finke, P.E.5
Miller, D.J.6
Budha, R.J.7
Cascieri, M.A.8
Sadowski, S.9
Strader, C.D.10
-
17
-
-
0019061918
-
LIGAND: A versatile computerized approach for characterization of ligand binding systems
-
Munson, P.J. and Rodbard, D., 1980. LIGAND: a versatile computerized approach for characterization of ligand binding systems. Anal. Biochem. 107, 220-239.
-
(1980)
Anal. Biochem.
, vol.107
, pp. 220-239
-
-
Munson, P.J.1
Rodbard, D.2
-
18
-
-
0026777534
-
Antiinflammatory and analgesic activity of a non-peptide substance P receptor antagonist
-
Nagahisa, A., Kanai, Y., Suga, O., Taniguchi, K., Tsuchiya, M., Lowe, J.A., Hess, H.-J., 1992. Antiinflammatory and analgesic activity of a non-peptide substance P receptor antagonist. Eur. J. Pharmacol. 217, 191-195.
-
(1992)
Eur. J. Pharmacol.
, vol.217
, pp. 191-195
-
-
Nagahisa, A.1
Kanai, Y.2
Suga, O.3
Taniguchi, K.4
Tsuchiya, M.5
Lowe, J.A.6
Hess, H.-J.7
-
19
-
-
0028235782
-
Differentiation between binding sites for angiotensin II and nonpeptide antagonists on the angiotensin II type 1 receptors
-
Schambye, H.T., Hjorth, S.A., Bergsma, D.J., Sathe, G., Schwartz, T.W., 1994a. Differentiation between binding sites for angiotensin II and nonpeptide antagonists on the angiotensin II type 1 receptors. Proc. Natl. Acad. Sci. USA 91, 7046-7050.
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 7046-7050
-
-
Schambye, H.T.1
Hjorth, S.A.2
Bergsma, D.J.3
Sathe, G.4
Schwartz, T.W.5
-
20
-
-
0028131452
-
1 receptor differentiate between closely related insurmountable and competitive angiotensin antagonists
-
1 receptor differentiate between closely related insurmountable and competitive angiotensin antagonists. Br. J. Pharmacol. 113, 331-333.
-
(1994)
Br. J. Pharmacol.
, vol.113
, pp. 331-333
-
-
Schambye, H.T.1
Wijk, B.2
Hjorth, S.A.3
Wienen, W.4
Entzeroth, M.5
Bergsma, D.J.6
Schwartz, T.W.7
-
21
-
-
0026099914
-
1) receptor
-
1) receptor. Science 251, 435-437.
-
(1991)
Science
, vol.251
, pp. 435-437
-
-
Snider, R.M.1
Constantine, J.W.2
Lowe, J.A.3
Longo, K.P.4
Lebel, W.S.5
Woody, H.A.6
Drozda, S.E.7
Desai, M.C.8
Vinick, F.J.9
Spencer, R.W.10
Hess, H.-J.11
-
22
-
-
0028269199
-
Enantioselective inhibition of apomorphine-induced emesis in the ferret by the neurokinin-1 receptor antagonist CP 99,994
-
Tattersall, F.D., Rycroft, W., Hill, R.G., Hargreaves, R.J., 1994. Enantioselective inhibition of apomorphine-induced emesis in the ferret by the neurokinin-1 receptor antagonist CP 99,994. Neuropharmacology 33, 259-260.
-
(1994)
Neuropharmacology
, vol.33
, pp. 259-260
-
-
Tattersall, F.D.1
Rycroft, W.2
Hill, R.G.3
Hargreaves, R.J.4
|