-
2
-
-
0027397351
-
Tachykinin receptors and tachykinin receptors antagonists
-
Maggi, C.A., Patacchini, R., Rovero, P., Giachetti, A. Tachykinin receptors and tachykinin receptors antagonists. J Auton Pharmacol 1993, 13: 23-93.
-
(1993)
J Auton Pharmacol
, vol.13
, pp. 23-93
-
-
Maggi, C.A.1
Patacchini, R.2
Rovero, P.3
Giachetti, A.4
-
3
-
-
0023898089
-
Local effector functions of capsaicin-sensitive sensory nerve endings: Involvement of tachykinins, calcitonin gene-related peptide and other neuropeptides
-
Holzer, P. Local effector functions of capsaicin-sensitive sensory nerve endings: Involvement of tachykinins, calcitonin gene-related peptide and other neuropeptides. Neuroscience 1988, 24: 739-68.
-
(1988)
Neuroscience
, vol.24
, pp. 739-768
-
-
Holzer, P.1
-
4
-
-
0027523466
-
Neurotransmitter functions of mammalian tachykinins
-
Otsuka, M., Yoshioka, K. Neurotransmitter functions of mammalian tachykinins. Physiol Rev 1993, 73: 229-308.
-
(1993)
Physiol Rev
, vol.73
, pp. 229-308
-
-
Otsuka, M.1
Yoshioka, K.2
-
5
-
-
0028905302
-
Neuropeptides as regulators of airway function: Vasoactive intestinal peptide and the tachykinins
-
Maggi, C.A., Giachetti, A., Dey, R.D., Said, S.I. Neuropeptides as regulators of airway function: Vasoactive intestinal peptide and the tachykinins. Physiol Rev 1995, 75: 277-322.
-
(1995)
Physiol Rev
, vol.75
, pp. 277-322
-
-
Maggi, C.A.1
Giachetti, A.2
Dey, R.D.3
Said, S.I.4
-
6
-
-
0030106240
-
Tachykinins in the autonomic nervous system
-
Maggi, C.A. Tachykinins in the autonomic nervous system. Pharm Res 1996, 33: 161-70.
-
(1996)
Pharm Res
, vol.33
, pp. 161-170
-
-
Maggi, C.A.1
-
7
-
-
0003155094
-
Historical perspectives of tachykinins
-
Buch, S.H. (Ed.). Humana Press: Totowa, NJ
-
Maggio, J.E., Mantyh, P.W., Iversen, L.L. Historical perspectives of tachykinins. In: The Tachykinin Receptors. Buch, S.H. (Ed.). Humana Press: Totowa, NJ 1994, 1-38.
-
(1994)
The Tachykinin Receptors
, pp. 1-38
-
-
Maggio, J.E.1
Mantyh, P.W.2
Iversen, L.L.3
-
8
-
-
0026099914
-
A potent non-peptide antagonist of the substance P (NK-1) receptor
-
Snider, R.M., Constantine, S.J.W., Lowe, J.A. et al. A potent non-peptide antagonist of the substance P (NK-1) receptor. Science 1991, 251: 435-7.
-
(1991)
Science
, vol.251
, pp. 435-437
-
-
Snider, R.M.1
Constantine, S.J.W.2
Lowe, J.A.3
-
9
-
-
0026559255
-
Synthesis of RP-67580, a new potent nonpeptide substance P antagonist
-
Peyronel, J.F., Truchon, A., Moutonnier, C., Garret, C. Synthesis of RP-67580, a new potent nonpeptide substance P antagonist. Bioorg & Med Chem Lett 1992, 2: 37-40.
-
(1992)
Bioorg & Med Chem Lett
, vol.2
, pp. 37-40
-
-
Peyronel, J.F.1
Truchon, A.2
Moutonnier, C.3
Garret, C.4
-
10
-
-
0026508416
-
A potent and selective non-peptide antagonist of the neurokinin a (NK-2) receptor
-
Edmonds-Alt, X., Vilain, P., Goulaouic, P. et al. A potent and selective non-peptide antagonist of the neurokinin A (NK-2) receptor. Life Sci 1992, 50: PL-101-6.
-
(1992)
Life Sci
, vol.50
-
-
Edmonds-Alt, X.1
Vilain, P.2
Goulaouic, P.3
-
12
-
-
0027175837
-
Tachykinin receptors: A radioligand binding perspective
-
Mussap, C.J., Geraghty, D.P., Burcher, E. Tachykinin receptors: A radioligand binding perspective. J Neurochem 1993, 60: 1987-2009.
-
(1993)
J Neurochem
, vol.60
, pp. 1987-2009
-
-
Mussap, C.J.1
Geraghty, D.P.2
Burcher, E.3
-
13
-
-
0027296875
-
Neurokinin receptor antagonists
-
McElroy, A.B. Neurokinin receptor antagonists. Curr Opin Ther Patents 1993, 3: 1157-72.
-
(1993)
Curr Opin Ther Patents
, vol.3
, pp. 1157-1172
-
-
McElroy, A.B.1
-
14
-
-
0028273239
-
Recent advances in the discovery and characterization of substance P antagonists
-
Desai, M.C. Recent advances in the discovery and characterization of substance P antagonists. Exp Opin Ther Patents 1994, 4: 315-21.
-
(1994)
Exp Opin Ther Patents
, vol.4
, pp. 315-321
-
-
Desai, M.C.1
-
15
-
-
0029613855
-
Tachykinin NK-3 receptors: Biology and development of selective peptide and nonpeptide ligands
-
Pritchard, M.C., Boden, P. Tachykinin NK-3 receptors: Biology and development of selective peptide and nonpeptide ligands. Drugs Fut 1995, 20: 1163-73.
-
(1995)
Drugs Fut
, vol.20
, pp. 1163-1173
-
-
Pritchard, M.C.1
Boden, P.2
-
16
-
-
0029965325
-
Neurokinin receptor antagonists
-
Swain, C. Neurokinin receptor antagonists. Exp Opin Ther Patents 1996, 6: 367-78.
-
(1996)
Exp Opin Ther Patents
, vol.6
, pp. 367-378
-
-
Swain, C.1
-
17
-
-
0029658344
-
Nonpeptide tachykinin antagonists: Medicinal chemistry and molecular biology
-
Lowe, J.A. III. Nonpeptide tachykinin antagonists: Medicinal chemistry and molecular biology. Med Res Rev 1996, 16: 527-45.
-
(1996)
Med Res Rev
, vol.16
, pp. 527-545
-
-
Lowe III, J.A.1
-
18
-
-
0001224776
-
Neurokinin receptor antagonists
-
Bristol, J.A. (Ed.). Academic Press: San Diego
-
Swain, C.J., Hargreaves, R.J. Neurokinin receptor antagonists. In: Annual Reports in Medicinal Chemistry, Vol. 31. Bristol, J.A. (Ed.). Academic Press: San Diego 1996, 111-20.
-
(1996)
Annual Reports in Medicinal Chemistry
, vol.31
, pp. 111-120
-
-
Swain, C.J.1
Hargreaves, R.J.2
-
21
-
-
0011177063
-
Structure and function of G-protein coupled receptors
-
Allen, R.C. (Ed.). Academic Press: San Diego
-
Dixon, R.A.F., Strader, C.D., Sigal, I.S. Structure and function of G-protein coupled receptors. In: Annual Reports in Medicinal Chemistry, Vol. 23. Allen, R.C. (Ed.). Academic Press: San Diego 1988, 221-33.
-
(1988)
Annual Reports in Medicinal Chemistry
, vol.23
, pp. 221-233
-
-
Dixon, R.A.F.1
Strader, C.D.2
Sigal, I.S.3
-
22
-
-
0024549304
-
Structure of adrenergic and related receptors
-
O'Dowd, B.F., Lefkowitz, R.J., Caron, M.G. Structure of adrenergic and related receptors. Annu Rev Neurosci 1989, 12: 67-83.
-
(1989)
Annu Rev Neurosci
, vol.12
, pp. 67-83
-
-
O'Dowd, B.F.1
Lefkowitz, R.J.2
Caron, M.G.3
-
23
-
-
0024560588
-
The molecular basis of muscarinic receptor diversity
-
Bonner, T.I. The molecular basis of muscarinic receptor diversity. Trends Neurosci 1989, 12: 148-51.
-
(1989)
Trends Neurosci
, vol.12
, pp. 148-151
-
-
Bonner, T.I.1
-
24
-
-
0025997478
-
Molecular cloning, structure characterization and functional expression of the human substance P receptor
-
Takeda, Y., Chou, K.B., Takeda, J., Sachais, B.S., Krause, J.E. Molecular cloning, structure characterization and functional expression of the human substance P receptor. Biochem Biophys Res Commun 1991, 179: 1232-40.
-
(1991)
Biochem Biophys Res Commun
, vol.179
, pp. 1232-1240
-
-
Takeda, Y.1
Chou, K.B.2
Takeda, J.3
Sachais, B.S.4
Krause, J.E.5
-
25
-
-
0024443851
-
Molecular characterization of a functional cDNa for rat substance P receptor
-
Yokota, Y., Sasai, Y., Tanaka, K. et al. Molecular characterization of a functional cDNA for rat substance P receptor. J Biol Chem 1989, 254: 17649-52.
-
(1989)
J Biol Chem
, vol.254
, pp. 17649-17652
-
-
Yokota, Y.1
Sasai, Y.2
Tanaka, K.3
-
26
-
-
0025091957
-
Molecular characterization of a functional cDNA encoding the rat substance P receptor and expression of its mRNA
-
Hershey, A.D., Krause, J.E. Molecular characterization of a functional cDNA encoding the rat substance P receptor and expression of its mRNA. Science 1990, 247: 958-61.
-
(1990)
Science
, vol.247
, pp. 958-961
-
-
Hershey, A.D.1
Krause, J.E.2
-
27
-
-
0023636772
-
CDNA cloning of bovine substance K receptor through oocyte expression system
-
Masu, Y., Nakayama, K., Tamaki, H., Harada, Y. Kuno, M., Nakanishi, S. cDNA cloning of bovine substance K receptor through oocyte expression system. Nature 1987, 329: 836-8.
-
(1987)
Nature
, vol.329
, pp. 836-838
-
-
Masu, Y.1
Nakayama, K.2
Tamaki, H.3
Harada, Y.4
Kuno, M.5
Nakanishi, S.6
-
28
-
-
0025242345
-
The human neurokinin a (substance K) receptor
-
Gerard, N.P., Eddy, R.L. Jr., Shows, T.B., Gerard, C. The human neurokinin A (substance K) receptor. J Biol Chem 1990, 265: 20455-62.
-
(1990)
J Biol Chem
, vol.265
, pp. 20455-20462
-
-
Gerard, N.P.1
Eddy Jr., R.L.2
Shows, T.B.3
Gerard, C.4
-
29
-
-
0024786847
-
Molecular characterization of rat substance K receptor and its mRNAs
-
Sasai, Y., Nakanishi, S. Molecular characterization of rat substance K receptor and its mRNAs. Biochem Biophys Res Commun 1989, 165: 695-702.
-
(1989)
Biochem Biophys Res Commun
, vol.165
, pp. 695-702
-
-
Sasai, Y.1
Nakanishi, S.2
-
30
-
-
0025128781
-
Cloning and expression of rat neuromedin K receptor cDNA
-
Shigemoto, R., Yokota, Y., Tsuchida, K., Nakanishi, S. Cloning and expression of rat neuromedin K receptor cDNA. J Biol Chem 1990, 265: 623-8.
-
(1990)
J Biol Chem
, vol.265
, pp. 623-628
-
-
Shigemoto, R.1
Yokota, Y.2
Tsuchida, K.3
Nakanishi, S.4
-
31
-
-
0026546277
-
Molecular characterization, expression and localization of human NK-3 receptor
-
Buell, G., Schulz, M.F., Arkinstall, S.J. et al. Molecular characterization, expression and localization of human NK-3 receptor. FEBS Lett 1992, 299: 90-5.
-
(1992)
FEBS Lett
, vol.299
, pp. 90-95
-
-
Buell, G.1
Schulz, M.F.2
Arkinstall, S.J.3
-
32
-
-
0026710633
-
CDNA sequence and heterologous expression of the human neurokinin-3 receptor
-
Huang, R.-R.C., Cheung, A.M., Mazina, K.E., Strader, C.D., Fong, T.M. cDNA sequence and heterologous expression of the human neurokinin-3 receptor. Biochem Biophys Res Commun 1992, 184: 966-72.
-
(1992)
Biochem Biophys Res Commun
, vol.184
, pp. 966-972
-
-
Huang, R.-R.C.1
Cheung, A.M.2
Mazina, K.E.3
Strader, C.D.4
Fong, T.M.5
-
33
-
-
0026535813
-
The primary structure and gene organization of human substance P and neuromedin K receptors
-
Takahashi, K., Tanaka, A., Hara, M., Nakanishi, S. The primary structure and gene organization of human substance P and neuromedin K receptors. Eur J Biochem 1992, 204: 1025-33.
-
(1992)
Eur J Biochem
, vol.204
, pp. 1025-1033
-
-
Takahashi, K.1
Tanaka, A.2
Hara, M.3
Nakanishi, S.4
-
34
-
-
0028903624
-
Tachykinin receptors and receptor subtypes
-
Patacchini, R., Maggi, C.A. Tachykinin receptors and receptor subtypes. Arch Int Pharmacodyn 1995, 329: 161-84.
-
(1995)
Arch Int Pharmacodyn
, vol.329
, pp. 161-184
-
-
Patacchini, R.1
Maggi, C.A.2
-
35
-
-
0028058897
-
Two NK-3 receptor subtypes: Demonstration by biological and binding assays
-
Nguyen, Q.T., Jukic, D., Chetien, L., Gobeil, F., Boussougou, M., Regoli, D. Two NK-3 receptor subtypes: Demonstration by biological and binding assays. Neuropeptides 1994, 27: 157-61.
-
(1994)
Neuropeptides
, vol.27
, pp. 157-161
-
-
Nguyen, Q.T.1
Jukic, D.2
Chetien, L.3
Gobeil, F.4
Boussougou, M.5
Regoli, D.6
-
36
-
-
0345650663
-
Evidence for NK-3 receptor subtypes in rabbit isolated iris sphincter muscle using the NK-3 receptor antagonists SR-142801 and SR-48968
-
Medhurst, A.D., Hay D.W.P., Parsons, A.A. Evidence for NK-3 receptor subtypes in rabbit isolated iris sphincter muscle using the NK-3 receptor antagonists SR-142801 and SR-48968. Br J Pharmacol 1996, 117: 203P.
-
(1996)
Br J Pharmacol
, vol.117
-
-
Medhurst, A.D.1
Hay, D.W.P.2
Parsons, A.A.3
-
37
-
-
0029837622
-
Functional characterization by heterologous expression of a novel cloned tachykinin peptide receptor
-
Donaldson, L.F., Haskell, C.A., Hanley, M.R. Functional characterization by heterologous expression of a novel cloned tachykinin peptide receptor. Biochem J 1996, 320: 1-5.
-
(1996)
Biochem J
, vol.320
, pp. 1-5
-
-
Donaldson, L.F.1
Haskell, C.A.2
Hanley, M.R.3
-
38
-
-
0025175645
-
Tissue distribution and quantification of the mRNA for three rat tachykinin receptors
-
Tsuchida, K., Shigemoto, R., Yokota, Y., Nakanishi, S. Tissue distribution and quantification of the mRNA for three rat tachykinin receptors. Eur J Biochem 1990, 193: 751-7.
-
(1990)
Eur J Biochem
, vol.193
, pp. 751-757
-
-
Tsuchida, K.1
Shigemoto, R.2
Yokota, Y.3
Nakanishi, S.4
-
39
-
-
0025674486
-
Localization of neuropeptide receptor mRNA in rat brain: Initial observations using probes for neurotensine and substance P receptors
-
Elde, R., Schalling, M., Ceccatelli, S., Nakanishi, S., Hokfelt, T. Localization of neuropeptide receptor mRNA in rat brain: Initial observations using probes for neurotensine and substance P receptors. Neurosci Lett 1990, 120: 134-8.
-
(1990)
Neurosci Lett
, vol.120
, pp. 134-138
-
-
Elde, R.1
Schalling, M.2
Ceccatelli, S.3
Nakanishi, S.4
Hokfelt, T.5
-
40
-
-
0026100201
-
Mammalian tachykinin receptors
-
Nakanishi, S. Mammalian tachykinin receptors. Annu Rev Neurosci 1991, 14: 123-36.
-
(1991)
Annu Rev Neurosci
, vol.14
, pp. 123-136
-
-
Nakanishi, S.1
-
41
-
-
0026060703
-
Phylogeny of tachykinin receptor localization in the vertebrate central nervous system
-
Dietl, M.M., Palacios, J.M. Phylogeny of tachykinin receptor localization in the vertebrate central nervous system. Brain Res 1991, 539: 211-22.
-
(1991)
Brain Res
, vol.539
, pp. 211-222
-
-
Dietl, M.M.1
Palacios, J.M.2
-
42
-
-
0027337632
-
Characterisation, CNS distribution and function of NK-2 receptors studied using potent NK-2 receptor antagonists
-
Hagan, R.M., Beresford, I.J.M., Stables, J. et al. Characterisation, CNS distribution and function of NK-2 receptors studied using potent NK-2 receptor antagonists. Regul Peptides 1993, 46: 9-19.
-
(1993)
Regul Peptides
, vol.46
, pp. 9-19
-
-
Hagan, R.M.1
Beresford, I.J.M.2
Stables, J.3
-
43
-
-
0001772001
-
GR-159897, a potent non-peptide tachykinin NK-2 receptor antagonist, releases suppressed behaviours in a novel aversive environment
-
Stratton, S.C., Beresford, I.J.M., Hagan, R.M. GR-159897, a potent non-peptide tachykinin NK-2 receptor antagonist, releases suppressed behaviours in a novel aversive environment. Br J Pharmacol 1994, 112: 49P.
-
(1994)
Br J Pharmacol
, vol.112
-
-
Stratton, S.C.1
Beresford, I.J.M.2
Hagan, R.M.3
-
44
-
-
0022856128
-
Characterization of a neurokinin B receptor site in rat brain using a highly selective radioligand
-
Laufer, R., Gilon, C., Chorevi, M., Selinger, Z. Characterization of a neurokinin B receptor site in rat brain using a highly selective radioligand. J Biol Chem 1986, 261: 10257-63.
-
(1986)
J Biol Chem
, vol.261
, pp. 10257-10263
-
-
Laufer, R.1
Gilon, C.2
Chorevi, M.3
Selinger, Z.4
-
45
-
-
0024157575
-
Localization of tachykinin binding sites (NK-1, NK-2, NK-3 ligands) in the rat brain
-
Saffroy, M., Beaujouan, J.-C., Torrens, Y., Besseyre, J., Bergström, L., Glowinski, J. Localization of tachykinin binding sites (NK-1, NK-2, NK-3 ligands) in the rat brain. Peptides 1988, 9: 227-41.
-
(1988)
Peptides
, vol.9
, pp. 227-241
-
-
Saffroy, M.1
Beaujouan, J.-C.2
Torrens, Y.3
Besseyre, J.4
Bergström, L.5
Glowinski, J.6
-
47
-
-
0026025836
-
Tachykinin receptor types: Classification and membrane signalling mechanisms
-
Guard, S., Watson, S.P. Tachykinin receptor types: Classification and membrane signalling mechanisms. Neurochem Int 1991, 18: 149-65.
-
(1991)
Neurochem Int
, vol.18
, pp. 149-165
-
-
Guard, S.1
Watson, S.P.2
-
48
-
-
0027293132
-
Inhibition of neurogenic inflammation in the meninges by a non-peptide tachykinin antagonist
-
Moussaoui, S.M. et al. Inhibition of neurogenic inflammation in the meninges by a non-peptide tachykinin antagonist. Eur J Pharmacol 1993, 238: 421-4.
-
(1993)
Eur J Pharmacol
, vol.238
, pp. 421-424
-
-
Moussaoui, S.M.1
-
49
-
-
0028869867
-
The non-peptide neurokinin-1 antagonist, RPR-100,893, decreases c-fos expression in trigeminal nucleus caudalis following noxious chemical meningeal stimulation
-
Cutrer, F.M. et al. The non-peptide neurokinin-1 antagonist, RPR-100,893, decreases c-fos expression in trigeminal nucleus caudalis following noxious chemical meningeal stimulation. Neuroscience 1995, 64: 741-50.
-
(1995)
Neuroscience
, vol.64
, pp. 741-750
-
-
Cutrer, F.M.1
-
50
-
-
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. Enantioselective inhibition of apomorphine-induced emesis in the ferret by the neurokinin-1 receptor antagonist CP-99,994. Neuropharmacology 1994, 33: 259-60.
-
(1994)
Neuropharmacology
, vol.33
, pp. 259-260
-
-
Tattersall, F.D.1
Rycroft, W.2
Hill, R.G.3
Hargreaves, R.J.4
-
51
-
-
0029065938
-
The antiemetic effects of CP-99,994 in the ferret and the dog - Role of the NK-1 receptor
-
Watson, J.W., Gonsalves, S.F., Fossa, A.A. et al. The antiemetic effects of CP-99,994 in the ferret and the dog - Role of the NK-1 receptor. Br J Pharmacol 1995, 115: 84-94.
-
(1995)
Br J Pharmacol
, vol.115
, pp. 84-94
-
-
Watson, J.W.1
Gonsalves, S.F.2
Fossa, A.A.3
-
52
-
-
2642664418
-
Tachykinin antagonists in the treatment of asthma
-
Lowe, J.A. III. Tachykinin antagonists in the treatment of asthma. Emerging Drugs 1996, 1-18.
-
(1996)
Emerging Drugs
, pp. 1-18
-
-
Lowe III, J.A.1
-
53
-
-
0027425533
-
Increased tachykinin receptor gene expression in asthmatic lung and its modulation by steroids
-
Adcock, I.M., Peters, M., Gelder, C., Shirasaki, H., Brown, C.R., Barnes, P.J. Increased tachykinin receptor gene expression in asthmatic lung and its modulation by steroids. J Mol Endocrinol 1993, 11: 1-7.
-
(1993)
J Mol Endocrinol
, vol.11
, pp. 1-7
-
-
Adcock, I.M.1
Peters, M.2
Gelder, C.3
Shirasaki, H.4
Brown, C.R.5
Barnes, P.J.6
-
54
-
-
0029360587
-
Substance P (NK-1)- and neurokinin a (NK-2) receptor gene expression in inflammatory airway diseases
-
Bai, T.R., Zhou, D., Weit, T. et al. Substance P (NK-1)- and neurokinin A (NK-2) receptor gene expression in inflammatory airway diseases. Am J Physiol 1995, 269: PL309-17.
-
(1995)
Am J Physiol
, vol.269
-
-
Bai, T.R.1
Zhou, D.2
Weit, T.3
-
55
-
-
0026628389
-
Effects of FK-224, a novel compound NK-1 and NK-2 receptor antagonist, on airway constriction and airway edema induced by neurokinins and sensory nerve stimulation in guinea-pigs
-
Murai, M., Morimoto, H., Maeda, Y., Kiyotoh, S., Nishikawa, M., Fujii, T. Effects of FK-224, a novel compound NK-1 and NK-2 receptor antagonist, on airway constriction and airway edema induced by neurokinins and sensory nerve stimulation in guinea-pigs. J Pharmacol Exp Ther 1992, 262: 403-8.
-
(1992)
J Pharmacol Exp Ther
, vol.262
, pp. 403-408
-
-
Murai, M.1
Morimoto, H.2
Maeda, Y.3
Kiyotoh, S.4
Nishikawa, M.5
Fujii, T.6
-
56
-
-
0029951892
-
The effect of inhaled FK-224, a tachykinin NK-1 and NK-2 receptor antagonist on neurokinin A-induced bronchoconstriction in asthmatics
-
Joos, G.F., Van Schoor, J., Kips, J.C., Pauwels, R.A. The effect of inhaled FK-224, a tachykinin NK-1 and NK-2 receptor antagonist on neurokinin A-induced bronchoconstriction in asthmatics. Am J Respir Crit Care Med 1996, 153: 1781-4.
-
(1996)
Am J Respir Crit Care Med
, vol.153
, pp. 1781-1784
-
-
Joos, G.F.1
Van Schoor, J.2
Kips, J.C.3
Pauwels, R.A.4
-
57
-
-
0026570879
-
The non-peptide tachykinin antagonist, CP-96,345, is a potent inhibitor of neurogenic inflammation
-
Lembeck, F., Donnerer, J., Tsuchiya, M., Nagahisa, A. The non-peptide tachykinin antagonist, CP-96,345, is a potent inhibitor of neurogenic inflammation. Br J Pharmacol 1992, 105: 527-30.
-
(1992)
Br J Pharmacol
, vol.105
, pp. 527-530
-
-
Lembeck, F.1
Donnerer, J.2
Tsuchiya, M.3
Nagahisa, A.4
-
58
-
-
0027339655
-
A non-peptide NK-1 receptor antagonist, RP-67580, inhibits neurogenic inflammation postsynaptically
-
Moussaoui, S.M., Montier, F., Carruette, A., Blanchard, J.C., Laduron, P.M., Garret, C. A non-peptide NK-1 receptor antagonist, RP-67580, inhibits neurogenic inflammation postsynaptically. Br J Pharmacol 1993, 109: 259-64.
-
(1993)
Br J Pharmacol
, vol.109
, pp. 259-264
-
-
Moussaoui, S.M.1
Montier, F.2
Carruette, A.3
Blanchard, J.C.4
Laduron, P.M.5
Garret, C.6
-
59
-
-
0027440588
-
Spinal cord amino acid release and content in an arthritis model: The effects of pretreatment with non-NMDA, NMDA, and NK-1 receptor antagonists
-
Sluka, K.A., Westlund, K.N. Spinal cord amino acid release and content in an arthritis model: The effects of pretreatment with non-NMDA, NMDA, and NK-1 receptor antagonists. Brain Res 1993, 627: 89-103.
-
(1993)
Brain Res
, vol.627
, pp. 89-103
-
-
Sluka, K.A.1
Westlund, K.N.2
-
60
-
-
0026801445
-
Broad spectrum neuropeptide antagonists inhibit the growth of small cell lung cancer in vivo
-
Langdon, S., Sethi, T., Ritchie, A. et al. Broad spectrum neuropeptide antagonists inhibit the growth of small cell lung cancer in vivo. Cancer Res 1992, 52: 4554-7.
-
(1992)
Cancer Res
, vol.52
, pp. 4554-4557
-
-
Langdon, S.1
Sethi, T.2
Ritchie, A.3
-
61
-
-
0027932625
-
Substance P binding sites on intestinal lymphoid aggregates and blood vessels in inflammatory bowel disease correspond to authentic NK-1 receptors
-
Mantyh, C.R., Vigna, S.R., Maggio, J.E., Mantyh, P.W., Bollinger, R.R., Pappas, T.N. Substance P binding sites on intestinal lymphoid aggregates and blood vessels in inflammatory bowel disease correspond to authentic NK-1 receptors. Neurosci Lett 1994, 178: 255-9.
-
(1994)
Neurosci Lett
, vol.178
, pp. 255-259
-
-
Mantyh, C.R.1
Vigna, S.R.2
Maggio, J.E.3
Mantyh, P.W.4
Bollinger, R.R.5
Pappas, T.N.6
-
62
-
-
0027926749
-
Blockade of tachykinin NK-1 receptors by CP-96,345 enhances dopamine release and the striatal dopamine effects of methamphetamine in rats
-
Gygi, S.P., Gibb, J.W., Johnson, M., Hanson, G.R. Blockade of tachykinin NK-1 receptors by CP-96,345 enhances dopamine release and the striatal dopamine effects of methamphetamine in rats. Eur J Pharmacol 1993, 250: 177-80.
-
(1993)
Eur J Pharmacol
, vol.250
, pp. 177-180
-
-
Gygi, S.P.1
Gibb, J.W.2
Johnson, M.3
Hanson, G.R.4
-
63
-
-
0028978250
-
2 receptor antagonist raclopride: Correlation with extracellular acethylcholine levels in striatum
-
2 receptor antagonist raclopride: Correlation with extracellular acethylcholine levels in striatum. J Pharmacol Exp Ther 1995, 274: 928-36.
-
(1995)
J Pharmacol Exp Ther
, vol.274
, pp. 928-936
-
-
Anderson, J.J.1
Randall, S.2
Chase, T.N.3
-
64
-
-
0027739666
-
Anxiolytic activity of tachykinin NK-2 receptor antagonists in the mouse light-dark box
-
Stratton, S.C., Beresford, I.J.M., Harvey, F.J., Turpin, M.P., Hagan, R.M., Tyers, M.B. Anxiolytic activity of tachykinin NK-2 receptor antagonists in the mouse light-dark box. Eur J Pharmacol 1993, 250: R11-2.
-
(1993)
Eur J Pharmacol
, vol.250
-
-
Stratton, S.C.1
Beresford, I.J.M.2
Harvey, F.J.3
Turpin, M.P.4
Hagan, R.M.5
Tyers, M.B.6
-
65
-
-
0025281419
-
Receptors for neurokinins in human bronchus and urinary bladder are of the NK-2 type
-
Dion, S., Rouissi, N., Nantel, F. et al. Receptors for neurokinins in human bronchus and urinary bladder are of the NK-2 type. Eur J Pharmacol 1990, 178: 215-9.
-
(1990)
Eur J Pharmacol
, vol.178
, pp. 215-219
-
-
Dion, S.1
Rouissi, N.2
Nantel, F.3
-
66
-
-
0025917690
-
NK-2 tachykinin receptors and contractions of circular muscle in the human colon: Characterization of the NK-2 receptor subtype
-
Giuliani, S., Barbanti, G., Turini, D. et al. NK-2 tachykinin receptors and contractions of circular muscle in the human colon: Characterization of the NK-2 receptor subtype. Eur J Pharmacol 1991, 203: 365-70.
-
(1991)
Eur J Pharmacol
, vol.203
, pp. 365-370
-
-
Giuliani, S.1
Barbanti, G.2
Turini, D.3
-
67
-
-
0027494856
-
Electrophysiological effects of tachykinins and capsaicin on guinea-pig bronchial parasympathetic neurons
-
Myers, A.C., Undem, B.J. Electrophysiological effects of tachykinins and capsaicin on guinea-pig bronchial parasympathetic neurons. J Physiol 1993, 470: 665-79.
-
(1993)
J Physiol
, vol.470
, pp. 665-679
-
-
Myers, A.C.1
Undem, B.J.2
-
68
-
-
0023607492
-
Sensory neuropeptide effects in human skin
-
Fuller, R.W., Conradson, T.-B., Dixon, C.M.S., Crossman, D.C., Barnes, P.J. Sensory neuropeptide effects in human skin. Br J Pharmacol 1987, 92: 781-8.
-
(1987)
Br J Pharmacol
, vol.92
, pp. 781-788
-
-
Fuller, R.W.1
Conradson, T.-B.2
Dixon, C.M.S.3
Crossman, D.C.4
Barnes, P.J.5
-
69
-
-
0023186979
-
Plasma protein extravasation induced by mammalian tachykinins in rat skin: Influence of anaesthetic agents and an acetylcholine antagonist
-
Couture, R., Kerouac, R. Plasma protein extravasation induced by mammalian tachykinins in rat skin: Influence of anaesthetic agents and an acetylcholine antagonist. Br J Pharmacol 1987, 91: 265-73.
-
(1987)
Br J Pharmacol
, vol.91
, pp. 265-273
-
-
Couture, R.1
Kerouac, R.2
-
70
-
-
0027976556
-
NK-1 and NK-3 type tachykinin receptor mRNA expression in the rat spinal cord dorsal horn is incresed during adjuvant or formalin-induced nociception
-
McCarson, K.E., Krause, J. NK-1 and NK-3 type tachykinin receptor mRNA expression in the rat spinal cord dorsal horn is incresed during adjuvant or formalin-induced nociception. J Neurosci 1994, 14: 712-20.
-
(1994)
J Neurosci
, vol.14
, pp. 712-720
-
-
McCarson, K.E.1
Krause, J.2
-
71
-
-
0026046314
-
Neurokinin receptors differentially mediate endogenous acetylcholine release evoked by tachykinins in the neostriatum
-
Arenas, E., Alberch, J., Perez-Navarro, E., Solsona, C., Marsal, J. Neurokinin receptors differentially mediate endogenous acetylcholine release evoked by tachykinins in the neostriatum. J Neurosci 1991, 11: 2332-8.
-
(1991)
J Neurosci
, vol.11
, pp. 2332-2338
-
-
Arenas, E.1
Alberch, J.2
Perez-Navarro, E.3
Solsona, C.4
Marsal, J.5
-
72
-
-
0029880569
-
Evidence for modulation of dopamine-neuronal function by tachykinin NK-3 receptor stimulation in gerbil mesencephalic cell cultures
-
Alonso, R., Fournier, M., Carayon, P., Petitpretre, G., Le Fur, G., Soubrié P. Evidence for modulation of dopamine-neuronal function by tachykinin NK-3 receptor stimulation in gerbil mesencephalic cell cultures. Eur J Neurosci 1996, 8: 801-8.
-
(1996)
Eur J Neurosci
, vol.8
, pp. 801-808
-
-
Alonso, R.1
Fournier, M.2
Carayon, P.3
Petitpretre, G.4
Le Fur, G.5
Soubrié, P.6
-
73
-
-
0023807704
-
The NK-3 tachykinin receptor agonist senktide elicits 5-HT-mediated behaviour following central or peripheral administration in mice and rats
-
Stoessl, A.J., Dourish, C.T., Iversen, S.D. The NK-3 tachykinin receptor agonist senktide elicits 5-HT-mediated behaviour following central or peripheral administration in mice and rats. Br J Pharmacol 1988, 94: 285-7.
-
(1988)
Br J Pharmacol
, vol.94
, pp. 285-287
-
-
Stoessl, A.J.1
Dourish, C.T.2
Iversen, S.D.3
-
74
-
-
0025309254
-
Pharmacological characterization of the behavioural syndrome induced by the NK-3 tachykinin agonist senktide in rodents: Evidence for mediation by endogenous 5-HT
-
Stoessl, A.J., Dourish, C.T., Iversen, S.D. Pharmacological characterization of the behavioural syndrome induced by the NK-3 tachykinin agonist senktide in rodents: Evidence for mediation by endogenous 5-HT. Brain Res 1990, 517: 111-6.
-
(1990)
Brain Res
, vol.517
, pp. 111-116
-
-
Stoessl, A.J.1
Dourish, C.T.2
Iversen, S.D.3
-
75
-
-
0027272974
-
Block of voltage-operated sodium currents by the substance P receptor antagonist (±)-CP-96,345 in neurones cultured from rat cortex
-
Caeser, M., Seabrook, G.R., Kemp, J.A. Block of voltage-operated sodium currents by the substance P receptor antagonist (±)-CP-96,345 in neurones cultured from rat cortex. Br J Pharmacol 1993, 109: 918-24.
-
(1993)
Br J Pharmacol
, vol.109
, pp. 918-924
-
-
Caeser, M.1
Seabrook, G.R.2
Kemp, J.A.3
-
76
-
-
0027215638
-
Nuclear variations of quinuclidine substance P antagonists: 2-Diphenylmethyl-1-azabicyclo[3.2.2]nonan-3-amines
-
Lowe, J.A., Drozda, S.E., Snider, R.M., Longo, K.P., Rizzi, J.P. Nuclear variations of quinuclidine substance P antagonists: 2-Diphenylmethyl-1-azabicyclo[3.2.2]nonan-3-amines. Bioorg & Med Chem Lett 1993, 3: 921-4.
-
(1993)
Bioorg & Med Chem Lett
, vol.3
, pp. 921-924
-
-
Lowe, J.A.1
Drozda, S.E.2
Snider, R.M.3
Longo, K.P.4
Rizzi, J.P.5
-
77
-
-
2642686535
-
-
Pfizer Inc. WO 9300330
-
O'Neill, B.T. Pfizer Inc. WO 9300330.
-
-
-
O'Neill, B.T.1
-
78
-
-
0027937012
-
Aza-tricyclic substance P antagonists
-
Lowe, J.A., Drozda, S.E., McLean, S. et al. Aza-tricyclic substance P antagonists. J Med Chem 1994, 37: 2831-40.
-
(1994)
J Med Chem
, vol.37
, pp. 2831-2840
-
-
Lowe, J.A.1
Drozda, S.E.2
McLean, S.3
-
79
-
-
0027157571
-
Quinuclidine-based NK-1 antagonists 1: 3-Benzyloxy-1-azabicyclo[2.2.2]-octanes
-
Seward, E.M., Swain, C.J., Merchant, K.J. et al. Quinuclidine-based NK-1 antagonists 1: 3-Benzyloxy-1-azabicyclo[2.2.2]-octanes. Bioorg & Med Chem Lett 1993, 3: 1361-6.
-
(1993)
Bioorg & Med Chem Lett
, vol.3
, pp. 1361-1366
-
-
Seward, E.M.1
Swain, C.J.2
Merchant, K.J.3
-
80
-
-
0027202121
-
Quinuclidine-based NK-1 antagonists 2: Determination of the absolute stereochemical requirements
-
Swain, C.J., Seward, E.M., Sabin, V. et al. Quinuclidine-based NK-1 antagonists 2: Determination of the absolute stereochemical requirements. Bioorg & Med Chem Lett 1993, 3: 1703-6.
-
(1993)
Bioorg & Med Chem Lett
, vol.3
, pp. 1703-1706
-
-
Swain, C.J.1
Seward, E.M.2
Sabin, V.3
-
81
-
-
0028219679
-
2-Aryl-1-azabicyclo[2.2.2]octanes as novel nonpeptide substance P antagonists
-
Lowe, J.A., Ewing, F.E., Snider, R.M. et al. 2-Aryl-1-azabicyclo[2.2.2]octanes as novel nonpeptide substance P antagonists. Bioorg & Med Chem Lett 1994, 6: 839-42.
-
(1994)
Bioorg & Med Chem Lett
, vol.6
, pp. 839-842
-
-
Lowe, J.A.1
Ewing, F.E.2
Snider, R.M.3
-
82
-
-
0029045099
-
Quinuclidine-based NK-1 antagonists, the role of the benzhydryl
-
Swain, C.J., Fong, T.M., Haworth, S.N., Owen, S.N., Seward, E.M., Strader, C.D. Quinuclidine-based NK-1 antagonists, the role of the benzhydryl. Bioorg & Med Chem Lett 1995, 5: 1261-4.
-
(1995)
Bioorg & Med Chem Lett
, vol.5
, pp. 1261-1264
-
-
Swain, C.J.1
Fong, T.M.2
Haworth, S.N.3
Owen, S.N.4
Seward, E.M.5
Strader, C.D.6
-
83
-
-
0028867427
-
Identification of a series of 3-(benzyloxy)-1-azabiciclo[2.2.2]octane human NK-1 antagonists
-
Swain, C.J., Seward, E.M., Cascieri, M.A. et al. Identification of a series of 3-(benzyloxy)-1-azabiciclo[2.2.2]octane human NK-1 antagonists. J Med Chem 1995, 38: 4793-805.
-
(1995)
J Med Chem
, vol.38
, pp. 4793-4805
-
-
Swain, C.J.1
Seward, E.M.2
Cascieri, M.A.3
-
84
-
-
0027048485
-
Discovery of a potent substance P antagonist: Recognition of key molecular determinant
-
Desai, M.C., Lefkowitz, S.L., Thadeio, P.F., Longo, K.P., Snider, R.M. Discovery of a potent substance P antagonist: Recognition of key molecular determinant. J Med Chem 1992, 35: 4911-3.
-
(1992)
J Med Chem
, vol.35
, pp. 4911-4913
-
-
Desai, M.C.1
Lefkowitz, S.L.2
Thadeio, P.F.3
Longo, K.P.4
Snider, R.M.5
-
85
-
-
0027186206
-
Synthesis of (±)-CP-99,994: A highly potent substance P antagonist
-
Desai, M.C., Thadeio, P.F., Lefkowitz, S.L. Synthesis of (±)-CP-99,994: A highly potent substance P antagonist. Tetrahedron Lett 1993, 34: 5831-4.
-
(1993)
Tetrahedron Lett
, vol.34
, pp. 5831-5834
-
-
Desai, M.C.1
Thadeio, P.F.2
Lefkowitz, S.L.3
-
86
-
-
0027437887
-
3H]-cis-3-[(2-methoxy)benzylamino]-2-phenylpiperidine, a highly potent and selective substance P receptor antagonist radioligand
-
3H]-cis-3-[(2-methoxy)benzylamino]-2-phenylpiperidine, a highly potent and selective substance P receptor antagonist radioligand. J Med Chem 1993, 36: 3197-201.
-
(1993)
J Med Chem
, vol.36
, pp. 3197-3201
-
-
Rosen, T.1
Seegar, T.F.2
McLean, S.3
-
87
-
-
0028990953
-
Effect of an NK-1 receptor antagonist (CP-99,994) on hypertonic saline-induced bronchoconstriction and cough in male asthmatic subjects
-
Fahy, J.V., Wong, H.F., Geppetti, P. et al. Effect of an NK-1 receptor antagonist (CP-99,994) on hypertonic saline-induced bronchoconstriction and cough in male asthmatic subjects. Am J Respir Crit Care Med 1995, 152: 879-84.
-
(1995)
Am J Respir Crit Care Med
, vol.152
, pp. 879-884
-
-
Fahy, J.V.1
Wong, H.F.2
Geppetti, P.3
-
88
-
-
0027381126
-
The antiemetic profile of a non peptide neurokinin NK-1 receptor antagonist CP-99,994 in ferrets
-
Bountra, C., Bunce, K.T., Dale, T. et al. The antiemetic profile of a non peptide neurokinin NK-1 receptor antagonist CP-99,994 in ferrets. Eur J Pharmacol 1993, 249: R3-4.
-
(1993)
Eur J Pharmacol
, vol.249
-
-
Bountra, C.1
Bunce, K.T.2
Dale, T.3
-
89
-
-
0027926751
-
The tachykinin NK-1 receptor antagonist CP-99,994 attenuates cisplatin induced emesis in the ferret
-
Tattersall, F.D., Rycroft, W., Hargreaves, R.J., Hill, R.G. The tachykinin NK-1 receptor antagonist CP-99,994 attenuates cisplatin induced emesis in the ferret. Eur J Pharmacol 1993, 250: R5-6.
-
(1993)
Eur J Pharmacol
, vol.250
-
-
Tattersall, F.D.1
Rycroft, W.2
Hargreaves, R.J.3
Hill, R.G.4
-
90
-
-
0010372672
-
Evaluation of a neurokinin 1 antagonist. CP-99,994, in comparison to ibuprofen and placebo in the oral surgery model
-
Dionne, R.A., Max, M.B., Parada, S., Gordon, S.M., Maclean, D.B. Evaluation of a neurokinin 1 antagonist. CP-99,994, in comparison to ibuprofen and placebo in the oral surgery model. Clin Pharmacol Ther 1996, 59: 216.
-
(1996)
Clin Pharmacol Ther
, vol.59
, pp. 216
-
-
Dionne, R.A.1
Max, M.B.2
Parada, S.3
Gordon, S.M.4
Maclean, D.B.5
-
91
-
-
2642637823
-
Characterization of the interaction of the novel antagonist CP-122,721 with the NK-1 tachykinin receptor
-
Oct 16-18, Florence
-
Mclean, S., Fossa, A., Zorn, S., Rosen, T. Characterization of the interaction of the novel antagonist CP-122,721 with the NK-1 tachykinin receptor. Tachykinins '95 (Oct 16-18, Florence) 1995, 19.
-
(1995)
Tachykinins '95
, pp. 19
-
-
Mclean, S.1
Fossa, A.2
Zorn, S.3
Rosen, T.4
-
92
-
-
0029893106
-
Broad spectrum antiemetic effects of CP-122,721, a tachykinin NK-1 receptor antagonist in ferrets
-
Gonsalves, S., Watson, J., Ashton, C. Broad spectrum antiemetic effects of CP-122,721, a tachykinin NK-1 receptor antagonist in ferrets. Eur J Pharmacol 1996, 305: 181-5.
-
(1996)
Eur J Pharmacol
, vol.305
, pp. 181-185
-
-
Gonsalves, S.1
Watson, J.2
Ashton, C.3
-
93
-
-
0342862584
-
Dose-ranging anti-emetic trial of the NK-1 receptor antagonist CP-122,721: A new approach for acute and delayed emesis following cisplatin
-
Kris, M.G., Radford, J., Pizzo, B. et al. Dose-ranging anti-emetic trial of the NK-1 receptor antagonist CP-122,721: A new approach for acute and delayed emesis following cisplatin. Proc Am Clin Oncol 1996, 15: A1780.
-
(1996)
Proc Am Clin Oncol
, vol.15
-
-
Kris, M.G.1
Radford, J.2
Pizzo, B.3
-
94
-
-
0029585287
-
1 receptor antagonist, (2S,3S)-(2-methoxy-5-tetrazol-1-ylbenzyl)(2-phenylpiperidin-3-yl)amine (GR-203040), with potent antiemetic activity
-
1 receptor antagonist, (2S,3S)-(2-methoxy-5-tetrazol-1-ylbenzyl)(2-phenylpiperidin-3-yl)amine (GR-203040), with potent antiemetic activity. J Med Chem 1995, 38: 4985-92.
-
(1995)
J Med Chem
, vol.38
, pp. 4985-4992
-
-
Ward, P.1
Armour, D.R.2
Bays, D.E.3
-
95
-
-
17044461438
-
Tetrazole NK-1 receptor antagonists: The identification of an exceptionally potent orally active antiemetic compound
-
Armour, D.R., Chung, K.M., Congreve, M. et al. Tetrazole NK-1 receptor antagonists: The identification of an exceptionally potent orally active antiemetic compound. Bioorg & Med Chem Lett 1996, 6: 1015-20.
-
(1996)
Bioorg & Med Chem Lett
, vol.6
, pp. 1015-1020
-
-
Armour, D.R.1
Chung, K.M.2
Congreve, M.3
-
96
-
-
2642692595
-
Tachykinin NK-1 antagonists: A new approach for the control of emesis. Peptide Receptors
-
Montreal, Canada, VII.O.2
-
Ward, P., Gardner, C.J., Twissel, D.J. et al. Tachykinin NK-1 antagonists: A new approach for the control of emesis. Peptide Receptors. An International Multidisciplinary Symposium. Montreal, Canada 1996, VII.O.2.
-
(1996)
An International Multidisciplinary Symposium
-
-
Ward, P.1
Gardner, C.J.2
Twissel, D.J.3
-
97
-
-
0027997928
-
Piperidine ether based hNK-1 antagonists 1: Determination of the relative and absolute stereochemical requirements
-
Harrison, T., Williams, B.J., Swain, C.J., Ball, R.G. Piperidine ether based hNK-1 antagonists 1: Determination of the relative and absolute stereochemical requirements. Bioorg & Med Chem Lett 1994, 4: 2545-50.
-
(1994)
Bioorg & Med Chem Lett
, vol.4
, pp. 2545-2550
-
-
Harrison, T.1
Williams, B.J.2
Swain, C.J.3
Ball, R.G.4
-
98
-
-
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 neurokinin-1 receptor antagonist
-
Hale, J.J., Mills, S.G., MacCoss, M. et al. 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 neurokinin-1 receptor antagonist. J Med Chem 1996, 39: 1760-2.
-
(1996)
J Med Chem
, vol.39
, pp. 1760-1762
-
-
Hale, J.J.1
Mills, S.G.2
MacCoss, M.3
-
99
-
-
0028922834
-
4,4-Disubstituted piperidines. A new class of NK-1 antagonist
-
Stevenson, G.I., MacLeod, A., Huscroft, I., Cascieri, M.A., Sadowski, S., Baker, R. 4,4-Disubstituted piperidines. A new class of NK-1 antagonist. J Med Chem 1995, 38: 1264-6.
-
(1995)
J Med Chem
, vol.38
, pp. 1264-1266
-
-
Stevenson, G.I.1
MacLeod, A.2
Huscroft, I.3
Cascieri, M.A.4
Sadowski, S.5
Baker, R.6
-
100
-
-
8944260413
-
N-Heteroaryl-2-phenyl-3-(benzyloxy)piperidines: A novel class of potent orally active human NK-1 antagonists
-
Ladduwahetty, T., Baker, R., Cascieri, M.A. et al. N-Heteroaryl-2-phenyl-3-(benzyloxy)piperidines: A novel class of potent orally active human NK-1 antagonists. J Med Chem 1996, 39: 2907-14.
-
(1996)
J Med Chem
, vol.39
, pp. 2907-2914
-
-
Ladduwahetty, T.1
Baker, R.2
Cascieri, M.A.3
-
101
-
-
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. et al. 1,2,3-Trisubstituted cyclohexyl substance-P antagonists: Significance of the ring nitrogen in piperidine-based NK-1 receptor antagonists. Bioorg & Med Chem Lett 1995, 5: 1345-50.
-
(1995)
Bioorg & Med Chem Lett
, vol.5
, pp. 1345-1350
-
-
Mills, S.G.1
MacCoss, M.2
Underwood, D.3
-
102
-
-
0027722031
-
1,4-Diacylpiperazine-2-(S)-[(N-aminoalkyl)carboxamides] as novel, potent substance P receptor antagonists
-
Mills, S.G., Wu, M.T., MacCoss, M. et al. 1,4-Diacylpiperazine-2-(S)-[(N-aminoalkyl)carboxamides] as novel, potent substance P receptor antagonists. Bioorg & Med Chem Lett 1993, 3: 2707-12.
-
(1993)
Bioorg & Med Chem Lett
, vol.3
, pp. 2707-2712
-
-
Mills, S.G.1
Wu, M.T.2
MacCoss, M.3
-
103
-
-
0028964676
-
1,2,4-Triacylpiperidine substance P antagonists: Separation of affinities for the NK-1 receptor and the L-type calcium channel
-
Mills, S.G., MacCoss, M., Cascieri, M.A. et al. 1,2,4-Triacylpiperidine substance P antagonists: Separation of affinities for the NK-1 receptor and the L-type calcium channel. Bioorg & Med Chem Lett 1995, 5: 599-604.
-
(1995)
Bioorg & Med Chem Lett
, vol.5
, pp. 599-604
-
-
Mills, S.G.1
MacCoss, M.2
Cascieri, M.A.3
-
104
-
-
0030598679
-
SAR of 2-benzyl-4-aminopiperidines: CGP-49823, an orally and centrally active non-peptide NK-1 antagonist
-
Ofner, S., Hauser, K., Schilling, W., Vassout, A., Veenstra, S.J. SAR of 2-benzyl-4-aminopiperidines: CGP-49823, an orally and centrally active non-peptide NK-1 antagonist. Bioorg & Med Chem Lett 1996, 6: 1623-8.
-
(1996)
Bioorg & Med Chem Lett
, vol.6
, pp. 1623-1628
-
-
Ofner, S.1
Hauser, K.2
Schilling, W.3
Vassout, A.4
Veenstra, S.J.5
-
105
-
-
0027715202
-
In vitro and in vivo biological activities of SR-140,333, a novel potent non-peptide tachykinin NK-1 receptor antagonist
-
Edmonds-Alt, X., Doutremepuich, J.D., Healulme, M. et al. In vitro and in vivo biological activities of SR-140,333, a novel potent non-peptide tachykinin NK-1 receptor antagonist. Eur J Pharmacol 1993, 250: 403-13.
-
(1993)
Eur J Pharmacol
, vol.250
, pp. 403-413
-
-
Edmonds-Alt, X.1
Doutremepuich, J.D.2
Healulme, M.3
-
106
-
-
24544452698
-
Influence of the tachykinin NK-1 receptor antagonist, SR-140,333, and of colchicine on functions mediated by afferent C-fibres in the rat
-
Juranek, I., Lembeck, F. Influence of the tachykinin NK-1 receptor antagonist, SR-140,333, and of colchicine on functions mediated by afferent C-fibres in the rat. Proc Br Pharmacol 1994, P189.
-
(1994)
Proc Br Pharmacol
-
-
Juranek, I.1
Lembeck, F.2
-
107
-
-
0029143173
-
4,4-Diphenyl-7-perhydrothiapyrano[3,4-c]pyrrolone, a new series of substance P receptor antagonists
-
Grisoni, S., Huon, C., Peyronel, J-F. 4,4-Diphenyl-7-perhydrothiapyrano[3,4-c]pyrrolone, a new series of substance P receptor antagonists. Bioorg & Med Chem Lett 1995, 5: 1591-4.
-
(1995)
Bioorg & Med Chem Lett
, vol.5
, pp. 1591-1594
-
-
Grisoni, S.1
Huon, C.2
Peyronel, J.-F.3
-
111
-
-
0013688528
-
In vivo pharmacological properties of RPR-100893, a novel non-peptide antagonist of the human NK-1 receptor
-
Moussaoui, S.M., Monttier, F., Carruette, A., Fardin, V., Floch, A., Garret, C. In vivo pharmacological properties of RPR-100893, a novel non-peptide antagonist of the human NK-1 receptor. Neuropeptides 1994, 26: 35 (C7/7).
-
(1994)
Neuropeptides
, vol.26
, pp. 35
-
-
Moussaoui, S.M.1
Monttier, F.2
Carruette, A.3
Fardin, V.4
Floch, A.5
Garret, C.6
-
112
-
-
0028017410
-
Acyclic NK-1 antagonists: 2-Benzhydryl-2-aminoethyl ethers
-
Williams, B.J., Teall, M., McKenna, J. et al. Acyclic NK-1 antagonists: 2-Benzhydryl-2-aminoethyl ethers. Bioorg & Med Chem Lett 1994, 4: 1903-8.
-
(1994)
Bioorg & Med Chem Lett
, vol.4
, pp. 1903-1908
-
-
Williams, B.J.1
Teall, M.2
McKenna, J.3
-
113
-
-
0030576287
-
Linear amides as substance P antagonists
-
Teall, M., Harrison, T., Moseley, J.D., Owens, A.P., Sadowski, S., Cascieri, M.A. Linear amides as substance P antagonists. Bioorg & Med Chem Lett 1996, 6: 1585-8.
-
(1996)
Bioorg & Med Chem Lett
, vol.6
, pp. 1585-1588
-
-
Teall, M.1
Harrison, T.2
Moseley, J.D.3
Owens, A.P.4
Sadowski, S.5
Cascieri, M.A.6
-
114
-
-
13344283413
-
3-Aryl-1,2-diacetamidopropane derivatives as novel and potent NK-1 receptor antagonists
-
Hipskind, P.A., Howbert, J.J., Bruns, R.F. et al. 3-Aryl-1,2-diacetamidopropane derivatives as novel and potent NK-1 receptor antagonists. J Med Chem 1996, 39: 736-48.
-
(1996)
J Med Chem
, vol.39
, pp. 736-748
-
-
Hipskind, P.A.1
Howbert, J.J.2
Bruns, R.F.3
-
115
-
-
0028933748
-
Synthesis and biological evaluation of NK-1 antagonists derived from L-tryptophan
-
MacLeod, A.M., Cascieri, M.A., Merchant, K.J. et al. Synthesis and biological evaluation of NK-1 antagonists derived from L-tryptophan. J Med Chem 1995, 38: 934-41.
-
(1995)
J Med Chem
, vol.38
, pp. 934-941
-
-
MacLeod, A.M.1
Cascieri, M.A.2
Merchant, K.J.3
-
116
-
-
0029098964
-
Novel potent, and orally active substance P antagonists: Synthesis and antagonist activity of N-benzylcarboxamide derivatives of pyrido[3,4-b]pyridine
-
Natsugari, H., Ikeura, Y., Kiyota, Y. et al. Novel potent, and orally active substance P antagonists: Synthesis and antagonist activity of N-benzylcarboxamide derivatives of pyrido[3,4-b]pyridine. J Med Chem 1995, 38: 3106-20.
-
(1995)
J Med Chem
, vol.38
, pp. 3106-3120
-
-
Natsugari, H.1
Ikeura, Y.2
Kiyota, Y.3
-
117
-
-
0026808484
-
Pharmacological profile of a high affinity dipeptide NK-1 receptor antagonist. FK-888
-
Fujii, T., Murai, M., Morimoto, H. et al. Pharmacological profile of a high affinity dipeptide NK-1 receptor antagonist. FK-888. Br J Pharmacol 1992, 107: 785-9.
-
(1992)
Br J Pharmacol
, vol.107
, pp. 785-789
-
-
Fujii, T.1
Murai, M.2
Morimoto, H.3
-
118
-
-
9044235778
-
A neurokinin 1 receptor antagonist improves exercise-induced airway narrowing in asthmatic patients
-
Ichinose, M., Motohiko, M., Yamauchi, H. et al. A neurokinin 1 receptor antagonist improves exercise-induced airway narrowing in asthmatic patients. Am J Respir Crit Care Med 1996, 153: 936-41.
-
(1996)
Am J Respir Crit Care Med
, vol.153
, pp. 936-941
-
-
Ichinose, M.1
Motohiko, M.2
Yamauchi, H.3
-
119
-
-
0028434993
-
Rational design of high affinity tachykinin NK-1 receptor antagonists
-
Boyle, S., Guard, S., Higginbottom, M. et al. Rational design of high affinity tachykinin NK-1 receptor antagonists. Bioorg & Med Chem Lett 1994, 2: 357-70.
-
(1994)
Bioorg & Med Chem Lett
, vol.2
, pp. 357-370
-
-
Boyle, S.1
Guard, S.2
Higginbottom, M.3
-
120
-
-
0030273630
-
Use of the chemical structure of peptides as the starting point to design non-peptide agonists and antagonists at peptide receptors: Examples with cholecystokinin and tachykinins
-
Horwell, D.C. Use of the chemical structure of peptides as the starting point to design non-peptide agonists and antagonists at peptide receptors: Examples with cholecystokinin and tachykinins. Bioorg & Med Chem 1996, 4: 1573-6.
-
(1996)
Bioorg & Med Chem
, vol.4
, pp. 1573-1576
-
-
Horwell, D.C.1
-
121
-
-
0008924831
-
SR-48,968, a potent and selective non-peptide antagonist of the neurokinin a (NK-2) receptor
-
Advenier, C., Emonds-Alt, X., Vilain, P. et al. SR-48,968, a potent and selective non-peptide antagonist of the neurokinin A (NK-2) receptor. Br J Pharmacol 1992, 105: 77P.
-
(1992)
Br J Pharmacol
, vol.105
-
-
Advenier, C.1
Emonds-Alt, X.2
Vilain, P.3
-
122
-
-
0027282693
-
The nonpeptide NK-2 antagonist SR-48,968 is also a NK-3 antagonist in the guinea pig but not in the rat
-
Petitet, F., Beaujouan, J.-C., Saffroy, M., Torrens, Y., Glowinski, J. The nonpeptide NK-2 antagonist SR-48,968 is also a NK-3 antagonist in the guinea pig but not in the rat. Biochem Biophys Res Commun 1993, 191: 180-7.
-
(1993)
Biochem Biophys Res Commun
, vol.191
, pp. 180-187
-
-
Petitet, F.1
Beaujouan, J.-C.2
Saffroy, M.3
Torrens, Y.4
Glowinski, J.5
-
123
-
-
0027270172
-
Pharmacological profile and chemical synthesis of SR-48,968, a non-peptide antagonist of the neurokinin a (NK-2) receptor
-
Emonds-Alt, X., Proietto, V., Van Broeck, D. et al. Pharmacological profile and chemical synthesis of SR-48,968, a non-peptide antagonist of the neurokinin A (NK-2) receptor. Bioorg & Med Chem Lett 1993, 3: 925-30.
-
(1993)
Bioorg & Med Chem Lett
, vol.3
, pp. 925-930
-
-
Emonds-Alt, X.1
Proietto, V.2
Van Broeck, D.3
-
124
-
-
0029904314
-
Parallell-compound synthesis: Methodology for accelerating drug discovery
-
Selway, C.N., Terrett, N.K. Parallell-compound synthesis: Methodology for accelerating drug discovery. Bioorg & Med Chem 1996, 4: 645-54.
-
(1996)
Bioorg & Med Chem
, vol.4
, pp. 645-654
-
-
Selway, C.N.1
Terrett, N.K.2
-
125
-
-
0029942633
-
A non-peptidic photoactivable antagonist for mapping the antagonist binding site of the tachykinin NK-2 receptor
-
Kersey, I.D., Bhogal, N., Donnelly, D., Fishwick, C.W.G., Findlay, J.B.C., Ward, C. A non-peptidic photoactivable antagonist for mapping the antagonist binding site of the tachykinin NK-2 receptor. Bioorg & Med Chem Lett 1996, 6: 605-8.
-
(1996)
Bioorg & Med Chem Lett
, vol.6
, pp. 605-608
-
-
Kersey, I.D.1
Bhogal, N.2
Donnelly, D.3
Fishwick, C.W.G.4
Findlay, J.B.C.5
Ward, C.6
-
126
-
-
0027512532
-
A facile synthesis of the novel neurokinin a antagonist SR-48,968
-
Hale, J.J., Finke, P.E., MacCoss, M. A facile synthesis of the novel neurokinin A antagonist SR-48,968. Bioorg & Med Chem Lett 1993, 3: 319-22.
-
(1993)
Bioorg & Med Chem Lett
, vol.3
, pp. 319-322
-
-
Hale, J.J.1
Finke, P.E.2
MacCoss, M.3
-
127
-
-
0026683346
-
Highly potent and selective heptapeptide antagonists of the neurokinin NK-2 receptor
-
McElroy, A.B., Clegg, S.P., Deal, M.J. et al. Highly potent and selective heptapeptide antagonists of the neurokinin NK-2 receptor. J Med Chem 1992, 35: 2582-91.
-
(1992)
J Med Chem
, vol.35
, pp. 2582-2591
-
-
McElroy, A.B.1
Clegg, S.P.2
Deal, M.J.3
-
128
-
-
0026592137
-
Conformationally constrained tachykinin analogues: Potent and highly selective neurokinin NK-2 receptor agonists
-
Deal, M.J., Hagan, R.M., Ireland, S.J. et al. Conformationally constrained tachykinin analogues: Potent and highly selective neurokinin NK-2 receptor agonists. J Med Chem 1992, 35: 4195-204.
-
(1992)
J Med Chem
, vol.35
, pp. 4195-4204
-
-
Deal, M.J.1
Hagan, R.M.2
Ireland, S.J.3
-
129
-
-
0027173587
-
Low-molecular-weight neurokinin NK-2 antagonists
-
Smith, P.W., McElroy, A.B., Pritchard, J.M. et al. Low-molecular-weight neurokinin NK-2 antagonists. Bioorg & Med Chem Lett 1993, 3: 931-6.
-
(1993)
Bioorg & Med Chem Lett
, vol.3
, pp. 931-936
-
-
Smith, P.W.1
McElroy, A.B.2
Pritchard, J.M.3
-
130
-
-
0028065313
-
GR159897 and related analogues as highly potent, orally active non-peptide neurokinin NK-2 receptor antagonists
-
Cooper, W.J., Adams, H.S., Bell, R. et al. GR159897 and related analogues as highly potent, orally active non-peptide neurokinin NK-2 receptor antagonists. Bioorg & Med Chem Lett 1994, 4: 1951-6.
-
(1994)
Bioorg & Med Chem Lett
, vol.4
, pp. 1951-1956
-
-
Cooper, W.J.1
Adams, H.S.2
Bell, R.3
-
131
-
-
0029146065
-
New spiropiperidines as potent and selective non-peptide tachykinin NK-2 receptor antagonists
-
Smith, P.W., Cooper, A.W., Bell, R. et al. New spiropiperidines as potent and selective non-peptide tachykinin NK-2 receptor antagonists. J Med Chem 1995, 38: 3772-9.
-
(1995)
J Med Chem
, vol.38
, pp. 3772-3779
-
-
Smith, P.W.1
Cooper, A.W.2
Bell, R.3
-
132
-
-
0028867134
-
Substituted 2,4-diaminoquinazolines and 2,4-diamino-8-alkylpurines as antagonists of the neurokinin-2 (NK-2) receptor
-
Jacobs, R.T., Mauger, R.C., Ulatowski, T.G., Aharony, D., Buckner, C.K. Substituted 2,4-diaminoquinazolines and 2,4-diamino-8-alkylpurines as antagonists of the neurokinin-2 (NK-2) receptor. Bioorg & Med Chem Lett 1995, 5: 2879-84.
-
(1995)
Bioorg & Med Chem Lett
, vol.5
, pp. 2879-2884
-
-
Jacobs, R.T.1
Mauger, R.C.2
Ulatowski, T.G.3
Aharony, D.4
Buckner, C.K.5
-
133
-
-
0029037956
-
Pharmacological characterization of a new class of nonpeptide neurokinin a antagonists that demonstrate species selectivity
-
Aharony, D., Buckner, C.K., Ellis, J.L. et al. Pharmacological characterization of a new class of nonpeptide neurokinin A antagonists that demonstrate species selectivity. J Pharmacol Exp Ther 1995, 274: 1216-21.
-
(1995)
J Pharmacol Exp Ther
, vol.274
, pp. 1216-1221
-
-
Aharony, D.1
Buckner, C.K.2
Ellis, J.L.3
-
134
-
-
0028373006
-
Rational design of high affinity tachykinin NK-2 receptor antagonists
-
Boyle, S., Guard, S., Hodgson, J. et al. Rational design of high affinity tachykinin NK-2 receptor antagonists. Bioorg & Med Chem 1994, 2: 101-13.
-
(1994)
Bioorg & Med Chem
, vol.2
, pp. 101-113
-
-
Boyle, S.1
Guard, S.2
Hodgson, J.3
-
135
-
-
0028101191
-
The rational development of small molecule tachykinin NK-3 receptor selective antagonists - The utilisation of a dipeptide chemical library in drug design
-
Boden, P., Eden, J.M., Hodgson, J. et al. The rational development of small molecule tachykinin NK-3 receptor selective antagonists - The utilisation of a dipeptide chemical library in drug design. Bioorg & Med Chem Lett 1994, 4: 1679-84.
-
(1994)
Bioorg & Med Chem Lett
, vol.4
, pp. 1679-1684
-
-
Boden, P.1
Eden, J.M.2
Hodgson, J.3
-
136
-
-
0029100579
-
The development of a novel series of non-peptide tachykinin NK-3 receptor selective antagonists
-
Boden, P., Eden, J.M., Hodgson, J. et al. The development of a novel series of non-peptide tachykinin NK-3 receptor selective antagonists. Bioorg & Med Chem Lett 1995, 5: 1773-8.
-
(1995)
Bioorg & Med Chem Lett
, vol.5
, pp. 1773-1778
-
-
Boden, P.1
Eden, J.M.2
Hodgson, J.3
-
137
-
-
15844384484
-
Use of a dipeptide chemical library in the development of non-peptide tachykinin NK-3 receptor selective antagonists
-
Boden, P., Eden, J.M., Hodgson, J. et al. Use of a dipeptide chemical library in the development of non-peptide tachykinin NK-3 receptor selective antagonists. J Med Chem 1996, 39: 1664-75.
-
(1996)
J Med Chem
, vol.39
, pp. 1664-1675
-
-
Boden, P.1
Eden, J.M.2
Hodgson, J.3
-
138
-
-
0028924764
-
SR-142,801, the first potent non-peptide antagonist of the tachykinin NK-3 receptor
-
Emonds-Alt, X., Bichon, D., Ducoux J.P. et al. SR-142,801, the first potent non-peptide antagonist of the tachykinin NK-3 receptor. Life Sci 1995, 56: PL 27-32.
-
(1995)
Life Sci
, vol.56
-
-
Emonds-Alt, X.1
Bichon, D.2
Ducoux, J.P.3
-
139
-
-
0029943956
-
Pharmacological characterization of SR-142801: A new non-peptide antagonist of the neurokinin NK-3 receptor
-
Nguyen-Le, X.K., Nguyen, Q.T., Gobeil, F. et al. Pharmacological characterization of SR-142801: A new non-peptide antagonist of the neurokinin NK-3 receptor. Pharmacology 1996, 52: 283-91.
-
(1996)
Pharmacology
, vol.52
, pp. 283-291
-
-
Nguyen-Le, X.K.1
Nguyen, Q.T.2
Gobeil, F.3
-
140
-
-
0030575607
-
A reliable and efficient synthesis of SR-142801
-
Giardina, G.A.M., Grugni, M., Rigolio, R., Vassallo, M., Erhard, K., Farina, C. A reliable and efficient synthesis of SR-142801. Bioorg & Med Chem Lett 1996, 6: 2307-10.
-
(1996)
Bioorg & Med Chem Lett
, vol.6
, pp. 2307-2310
-
-
Giardina, G.A.M.1
Grugni, M.2
Rigolio, R.3
Vassallo, M.4
Erhard, K.5
Farina, C.6
-
141
-
-
0031552139
-
A practical and scalable synthesis of SR-142801, a tachykinin NK-3 antagonist
-
Chen, H.G., Chung, F.-Z., Goel, O.P. et al. A practical and scalable synthesis of SR-142801, a tachykinin NK-3 antagonist. Bioorg & Med Chem Lett 1997, 7: 555-60.
-
(1997)
Bioorg & Med Chem Lett
, vol.7
, pp. 555-560
-
-
Chen, H.G.1
Chung, F.-Z.2
Goel, O.P.3
-
142
-
-
2642693613
-
-
Shah, S.K. (Merck & Co. Inc.). US 5434158
-
Shah, S.K. (Merck & Co. Inc.). US 5434158.
-
-
-
-
143
-
-
5244332801
-
2-Phenyl-4-quinoline carboxamides: A novel class of potent and selective non-peptide competitive antagonists for the human neurokinin-3 receptor
-
Giardina, G.A.M., Sarau, H.M., Farina, C. et al. 2-Phenyl-4-quinoline carboxamides: A novel class of potent and selective non-peptide competitive antagonists for the human neurokinin-3 receptor. J Med Chem 1996, 39: 2281-4.
-
(1996)
J Med Chem
, vol.39
, pp. 2281-2284
-
-
Giardina, G.A.M.1
Sarau, H.M.2
Farina, C.3
-
144
-
-
0345218872
-
Potent and selective non-peptide NK-3 receptor antagonists based on the quinoline framework
-
Sept 8-12, Maastricht, Abst P-2.15
-
Grugni, M., Farina, C., Giardina, G.A.M. et al. Potent and selective non-peptide NK-3 receptor antagonists based on the quinoline framework. XIVth Int Symp Med Chem (Sept 8-12, Maastricht) 1996, Abst P-2.15.
-
(1996)
XIVth Int Symp Med Chem
-
-
Grugni, M.1
Farina, C.2
Giardina, G.A.M.3
-
145
-
-
14444269664
-
Discovery of a novel class of selective nonpeptide antagonists for the human neurokinin-3 receptor. I. Identification of the 4-quinolinecarboxamide framework
-
Giardina, G.A.M., Sarau, H.M., Farina, C. et al. Discovery of a novel class of selective nonpeptide antagonists for the human neurokinin-3 receptor. I. Identification of the 4-quinolinecarboxamide framework. J Med Chem 1997, 40: 1794-807.
-
(1997)
J Med Chem
, vol.40
, pp. 1794-1807
-
-
Giardina, G.A.M.1
Sarau, H.M.2
Farina, C.3
-
146
-
-
2642589904
-
SB-223412, a novel quinoline NK-3 receptor antagonist with high potency, selectivity and oral activity
-
Sept 8-12, Maastricht, Abst OC-2/P-2.44
-
Giardina, G.A.M., Farina, C., Foley, J.J. et al. SB-223412, a novel quinoline NK-3 receptor antagonist with high potency, selectivity and oral activity. XIVth Int Symp Med Chem (Sept 8-12, Maastricht) 1996, Abst OC-2/P-2.44.
-
(1996)
XIVth Int Symp Med Chem
-
-
Giardina, G.A.M.1
Farina, C.2
Foley, J.J.3
-
147
-
-
15144349599
-
Nonpeptide tachykinin receptor antagonists. I. Pharmacological and pharmacokinetic characterization of SB-223412, a novel, potent and selective NK-3 receptor antagonist
-
Sarau, H.M., Griswold, D.E., Potts, W. et al. Nonpeptide tachykinin receptor antagonists. I. Pharmacological and pharmacokinetic characterization of SB-223412, a novel, potent and selective NK-3 receptor antagonist. J Pharmacol Exp Ther 1997, 281: 1303-11.
-
(1997)
J Pharmacol Exp Ther
, vol.281
, pp. 1303-1311
-
-
Sarau, H.M.1
Griswold, D.E.2
Potts, W.3
-
148
-
-
2642626541
-
Discovery of neurokinin antagonists
-
Takaya, T. Discovery of neurokinin antagonists. Pure Appl Chem 1996, 68: 875-80.
-
(1996)
Pure Appl Chem
, vol.68
, pp. 875-880
-
-
Takaya, T.1
-
149
-
-
0026444911
-
Protection against bradykinin-induced bronchoconstriction in asthmatic patients by neurokinin receptor antagonist
-
Ichinose, M., Nakajima, N., Takahashi, T. et al. Protection against bradykinin-induced bronchoconstriction in asthmatic patients by neurokinin receptor antagonist. Lancet 1992, 340: 1248-51.
-
(1992)
Lancet
, vol.340
, pp. 1248-1251
-
-
Ichinose, M.1
Nakajima, N.2
Takahashi, T.3
-
150
-
-
0029951892
-
The effect of inhaled FK-224, a tachykinin NK-1 and NK-2 receptor antagonist on neurokinin A-induced bronchoconstriction in asthmatics
-
Joos, G.F., Van Schoor, J., Kips, J.C., Pauwels, R.A. The effect of inhaled FK-224, a tachykinin NK-1 and NK-2 receptor antagonist on neurokinin A-induced bronchoconstriction in asthmatics. Am J Respir Crit Care Med 1996, 153: 1781-4.
-
(1996)
Am J Respir Crit Care Med
, vol.153
, pp. 1781-1784
-
-
Joos, G.F.1
Van Schoor, J.2
Kips, J.C.3
Pauwels, R.A.4
-
151
-
-
2642629597
-
Identification and chemical synthesis of MDL-105,212, a non-selective, non-peptide tachykinin receptor antagonist
-
Oct 16-18, Florence
-
Burkholder, T.P., Le, T.-B., Maynard, G.D., Shatzer, S.A., Knippenberg, R.W., Kudlacz, E.M. Identification and chemical synthesis of MDL-105,212, a non-selective, non-peptide tachykinin receptor antagonist. Tachykinins '95 Symposium (Oct 16-18, Florence) 1995, 21.
-
(1995)
Tachykinins '95 Symposium
, pp. 21
-
-
Burkholder, T.P.1
Le, T.-B.2
Maynard, G.D.3
Shatzer, S.A.4
Knippenberg, R.W.5
Kudlacz, E.M.6
-
152
-
-
0029873748
-
Identification and chemical synthesis of MDL-105,212, a non-peptide tachykinin antagonist with high affinity for NK-1 and NK-2 receptors
-
Burkholder, T.P., Kudlacz, E.M., Le, T.-B. et al. Identification and chemical synthesis of MDL-105,212, a non-peptide tachykinin antagonist with high affinity for NK-1 and NK-2 receptors. Bioorg & Med Chem Lett 1996, 6: 951-6.
-
(1996)
Bioorg & Med Chem Lett
, vol.6
, pp. 951-956
-
-
Burkholder, T.P.1
Kudlacz, E.M.2
Le, T.-B.3
-
153
-
-
2642657217
-
-
(Merck & Co., Inc.). WO 9417045
-
Hale, J.J., MacCoss, M., Mills, S.G., Qi, H., Shah, S.K. (Merck & Co., Inc.). WO 9417045.
-
-
-
Hale, J.J.1
MacCoss, M.2
Mills, S.G.3
Qi, H.4
Shah, S.K.5
-
154
-
-
2642667362
-
-
(Merck & Co., Inc.). WO 9429309
-
MacCoss, M., Mills, S.G., Shah, S.K. et al. (Merck & Co., Inc.). WO 9429309.
-
-
-
MacCoss, M.1
Mills, S.G.2
Shah, S.K.3
-
155
-
-
2642700886
-
-
(Merck & Co., Inc.). WO 9610568
-
Chiang, Y.-C.P., Finke, P.E., MacCoss, M. et al. (Merck & Co., Inc.). WO 9610568.
-
-
-
Chiang, Y.-C.P.1
Finke, P.E.2
MacCoss, M.3
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