-
1
-
-
0004360488
-
-
K. Bláha and P. Malon, Eds., de Gruyter, Berlin
-
Y. Ovchinikov, G. Chipens and V. Ivanov, in: Peptides 1982, K. Bláha and P. Malon, Eds., p. 1-18, de Gruyter, Berlin 1983.
-
(1983)
Peptides 1982
, pp. 1-18
-
-
Ovchinikov, Y.1
Chipens, G.2
Ivanov, V.3
-
2
-
-
0026155124
-
Backbone cyclizatlon: A new method for conferring conformational constraint on peptides
-
C. Gilon, D. Halle, M. Chorev, Z. Selinger and G. Byk (1991). Backbone cyclizatlon: A new method for conferring conformational constraint on peptides. Biopolymers 31, 745-750.
-
(1991)
Biopolymers
, vol.31
, pp. 745-750
-
-
Gilon, C.1
Halle, D.2
Chorev, M.3
Selinger, Z.4
Byk, G.5
-
3
-
-
2042462148
-
-
N. Yanaihara, Ed., ESCOM Science Publishers B.V., Leiden
-
C. Gilon, I. Zeltser, V. Rashti-Behar, D. Muller, G. Bitan, D. Halle, G. Bar-Akiva, Z. Selinger and G. Byk, in: Peptide Chemistry 1992, N. Yanaihara, Ed., p. 482-485, ESCOM Science Publishers B.V., Leiden 1993.
-
(1993)
Peptide Chemistry 1992
, pp. 482-485
-
-
Gilon, C.1
Zeltser, I.2
Rashti-Behar, V.3
Muller, D.4
Bitan, G.5
Halle, D.6
Bar-Akiva, G.7
Selinger, Z.8
Byk, G.9
-
4
-
-
33751391520
-
Building units for N-backbone cyclic peptides. 1. Synthesis of protected N-(ω-aminoalkyl) amino acids and their incorporation into dipeptide units
-
G. Byk and C. Gilon (1992). Building units for N-backbone cyclic peptides. 1. Synthesis of protected N-(ω-aminoalkyl) amino acids and their incorporation into dipeptide units. J. Org. Chem. 57, 5687-5691.
-
(1992)
J. Org. Chem.
, vol.57
, pp. 5687-5691
-
-
Byk, G.1
Gilon, C.2
-
5
-
-
0029025947
-
α-(ω-thioalkyl)amino acids and their incorporation into dipeptide units
-
α-(ω-thioalkyl)amino acids and their incorporation into dipeptide units. Tetrahedron 51, 10513-10522.
-
(1995)
Tetrahedron
, vol.51
, pp. 10513-10522
-
-
Bitan, G.1
Gilon, C.2
-
7
-
-
85033824338
-
-
(1994). Israeli Patent Application no. 109943; International Patent Application no. PCT/IB95/00453
-
C. Gilon, I. Zeltser, D. Muller, G. Bitan, D. Eren and A. Seri-Levi (1994). Israeli Patent Application no. 109943; International Patent Application no. PCT/IB95/00453.
-
-
-
Gilon, C.1
Zeltser, I.2
Muller, D.3
Bitan, G.4
Eren, D.5
Seri-Levi, A.6
-
8
-
-
0028589913
-
Receptors and antagonists for substance P and related peptides
-
D. Regoli, A. Boudon and J.-L. Fouchere (1994). Receptors and antagonists for substance P and related peptides. Pharmacol. Rev. 46, 551-559.
-
(1994)
Pharmacol. Rev.
, vol.46
, pp. 551-559
-
-
Regoli, D.1
Boudon, A.2
Fouchere, J.-L.3
-
9
-
-
0013511786
-
Neurokinin B is a preferred agonist for neuronal substance P receptor and its action is antagonized by enkephalin
-
R. Laufer, U. Wormser, Z. Y. Friedman, C. Gilon, M. Chorev and Z. Selinger (1985). Neurokinin B is a preferred agonist for neuronal substance P receptor and its action is antagonized by enkephalin. Proc. Natl Acad. Sci. USA 83, 7444-7448.
-
(1985)
Proc. Natl Acad. Sci. USA
, vol.83
, pp. 7444-7448
-
-
Laufer, R.1
Wormser, U.2
Friedman, Z.Y.3
Gilon, C.4
Chorev, M.5
Selinger, Z.6
-
10
-
-
0022816531
-
Highly selective agonists for substance P receptor subtypes
-
U. Wormser, R. Laufer, Y. Hart, M. Chorev, C. Gilon and Z. Selinger (1986). Highly selective agonists for substance P receptor subtypes. EMBO J. 5, 2805-2808.
-
(1986)
EMBO J.
, vol.5
, pp. 2805-2808
-
-
Wormser, U.1
Laufer, R.2
Hart, Y.3
Chorev, M.4
Gilon, C.5
Selinger, Z.6
-
11
-
-
0022856128
-
Characterization of a neurokinin B receptor site in rat brain using a highly selective radioligand
-
R. Laufer, C. Gilon, M. Chorev and Z. Selinger (1986). Characterization of a neurokinin B receptor site in rat brain using a highly selective radioligand. J. Biol. Chem. 261, 10257-10263.
-
(1986)
J. Biol. Chem.
, vol.261
, pp. 10257-10263
-
-
Laufer, R.1
Gilon, C.2
Chorev, M.3
Selinger, Z.4
-
12
-
-
0023878616
-
Desensitization with a selective agonist discriminates between multiple tachykinin receptors
-
R. Laufer, C. Gilon, M. Chorev and Z. Selinger (1986). Desensitization with a selective agonist discriminates between multiple tachykinin receptors. Pharmacol. Exp. Ther. 245, 639-643.
-
(1986)
Pharmacol. Exp. Ther.
, vol.245
, pp. 639-643
-
-
Laufer, R.1
Gilon, C.2
Chorev, M.3
Selinger, Z.4
-
14
-
-
0019505301
-
Synthesis and biological properties of enzyme resistant substance P analogues
-
B. E. Sandberg, C. M. Lee, M. R. Hanley and L. L. Iversen (1981). Synthesis and biological properties of enzyme resistant substance P analogues. Eur. J. Biochem. 114, 329-337.
-
(1981)
Eur. J. Biochem.
, vol.114
, pp. 329-337
-
-
Sandberg, B.E.1
Lee, C.M.2
Hanley, M.R.3
Iversen, L.L.4
-
15
-
-
0023243292
-
Specific agonists for neurokinin B receptors
-
G. Dupreau, P. D'Orleans-Juste, S. Dion, N. E. Rhaleb and D. Regoli (1987). Specific agonists for neurokinin B receptors. Eur. J. Pharmacol. 136, 401-403.
-
(1987)
Eur. J. Pharmacol.
, vol.136
, pp. 401-403
-
-
Dupreau, G.1
D'Orleans-Juste, P.2
Dion, S.3
Rhaleb, N.E.4
Regoli, D.5
-
16
-
-
0024311960
-
A potent and selective agonist for the NK-2 tachykinin receptor
-
P. Rovero, V. Pestellini, R. Patacchini, S. Giuliani, P. Santicioli, C. A. Maggi, A. Meli and A. Giachetti (1989). A potent and selective agonist for the NK-2 tachykinin receptor. Peptides 10, 593-595.
-
(1989)
Peptides
, vol.10
, pp. 593-595
-
-
Rovero, P.1
Pestellini, V.2
Patacchini, R.3
Giuliani, S.4
Santicioli, P.5
Maggi, C.A.6
Meli, A.7
Giachetti, A.8
-
17
-
-
0026592137
-
Conformationally constrained tachykinin analogues: Potent and highly selective NK-2 receptor agonists
-
M. J. Deal, R. M. Hagan, S. J. Ireland, C. C. Jordan, A. B. McElroy, B. Porter, B. C. Ross, M. Stephens-Smith and P. Ward (1992). Conformationally constrained tachykinin analogues: Potent and highly selective NK-2 receptor agonists. J. Med. Chem. 35, 4195-4204.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 4195-4204
-
-
Deal, M.J.1
Hagan, R.M.2
Ireland, S.J.3
Jordan, C.C.4
McElroy, A.B.5
Porter, B.6
Ross, B.C.7
Stephens-Smith, M.8
Ward, P.9
-
18
-
-
0023257815
-
Structure-activity studies on the C-terminal hexapeptide of substance P with modifications at the glutaminyl and methionyl residues
-
C. Poulos, G. Stavropoulos, J. R. Brown and C. C. Jordan (1987). Structure-activity studies on the C-terminal hexapeptide of substance P with modifications at the glutaminyl and methionyl residues. J. Med. Chem. 30, 1512-1515.
-
(1987)
J. Med. Chem.
, vol.30
, pp. 1512-1515
-
-
Poulos, C.1
Stavropoulos, G.2
Brown, J.R.3
Jordan, C.C.4
-
20
-
-
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 III, 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
-
21
-
-
0027048485
-
Discovery of a potent substance P antagonist: Recognition of the key molecular determinant
-
M. C. Desai, S. L. Lefkowitz, P. F. Thadeio, K. P. Longo and R. M. Snider (1992). Discovery of a potent substance P antagonist: Recognition of the key molecular determinant. J. Med. Chem. 35, 4911-4913.
-
(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
-
22
-
-
0025889015
-
Pharmacological properties of a potent and selective nonpeptide substance P antagonist
-
C. Garret, A. Carruette, V. Fardin, S. Moussaoui, J. Peyronel, J. Blanchard and P. Laduron (1992). Pharmacological properties of a potent and selective nonpeptide substance P antagonist. Proc. Natl Acad. Sci. USA 88, 10208-10212.
-
(1992)
Proc. Natl Acad. Sci. USA
, vol.88
, pp. 10208-10212
-
-
Garret, C.1
Carruette, A.2
Fardin, V.3
Moussaoui, S.4
Peyronel, J.5
Blanchard, J.6
Laduron, P.7
-
23
-
-
0028933748
-
1 antagonists derived from L-tryptophane
-
1 antagonists derived from L-tryptophane. J. Med. Chem. 38, 934-941.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 934-941
-
-
MacLeod, A.M.1
Cascieri, M.A.2
Merchant, K.J.3
Sadowski, S.4
Hardwicke, S.5
Lewis, R.T.6
MacIntyre, D.E.7
Metzger, J.8
Fong, T.M.9
Shepard, S.10
Tattersall, F.D.11
Hargreaves, R.12
Baker, R.13
-
24
-
-
0344447315
-
SR 140333, a novel and potent antagonist of the NK1 receptor characterization on the U373MG cell line
-
F. Oury-Donat, I. A. Lefevre, T. Gautier, X. Edmonds-Alt, G. Le Fur and P. Soubrie (1994). SR 140333, a novel and potent antagonist of the NK1 receptor characterization on the U373MG cell line. Neuropeptides 24, 233.
-
(1994)
Neuropeptides
, vol.24
, pp. 233
-
-
Oury-Donat, F.1
Lefevre, I.A.2
Gautier, T.3
Edmonds-Alt, X.4
Le Fur, G.5
Soubrie, P.6
-
25
-
-
0026470597
-
Nonpeptide peptidomimetics with a β-D-glucose scaffolding. A partial somatostatin agonist bearing a close structural relationship to a potent, selective substance P antagonist
-
R. Hirschmann, K. C. Nicolaou, S. Pietranico, J. Salvino, E. M. Leahy, P. A. Sprengeler, G. Furst, A. B. Smith III, C. D. Strader, M. A. Cascieri, M. R. Candelore, C. Donaldson, W. Vale and L. Maechler (1992). Nonpeptide peptidomimetics with a β-D-glucose scaffolding. A partial somatostatin agonist bearing a close structural relationship to a potent, selective substance P antagonist. J. Am. Chem. Soc. 114, 9217-9218.
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 9217-9218
-
-
Hirschmann, R.1
Nicolaou, K.C.2
Pietranico, S.3
Salvino, J.4
Leahy, E.M.5
Sprengeler, P.A.6
Furst, G.7
Smith III, A.B.8
Strader, C.D.9
Cascieri, M.A.10
Candelore, M.R.11
Donaldson, C.12
Vale, W.13
Maechler, L.14
-
27
-
-
0027402090
-
Amino-aromatic interaction between histidine 197 of the neurokinin-1 receptor and CP 96345
-
T. M. Fong, M. A. Cascieri, H. Yu, A. Bansal, C. Swain and C. D. Strader (1993). Amino-aromatic interaction between histidine 197 of the neurokinin-1 receptor and CP 96345. 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
-
28
-
-
0020200903
-
Conformational energy calculations on substance P
-
P. Manavalan and F. A. Momany (1982). Conformational energy calculations on substance P. Int. J. Peptide Protein Res. 20, 351-356.
-
(1982)
Int. J. Peptide Protein Res.
, vol.20
, pp. 351-356
-
-
Manavalan, P.1
Momany, F.A.2
-
29
-
-
0022497377
-
Preferential conformation of substance P in solution
-
G. Chassaing, O. Convert and S. Laville (1986). Preferential conformation of substance P in solution. Eur. J. Biochem. 154, 77-85.
-
(1986)
Eur. J. Biochem.
, vol.154
, pp. 77-85
-
-
Chassaing, G.1
Convert, O.2
Laville, S.3
-
30
-
-
0028019634
-
NMR and molecular modeling investigations of the neuropeptide substance P in the presence of 15 mM sodium dodecyl sulfate micelles
-
J. K. Young, C. Anklin and R. P. Hicks (1994). NMR and molecular modeling investigations of the neuropeptide substance P in the presence of 15 mM sodium dodecyl sulfate micelles. Biopolymers 34, 1449-1462.
-
(1994)
Biopolymers
, vol.34
, pp. 1449-1462
-
-
Young, J.K.1
Anklin, C.2
Hicks, R.P.3
-
32
-
-
0022376922
-
6-11 hexapeptide
-
6-11 hexapeptide. Pharmazie 40, 532-535.
-
(1985)
Pharmazie
, vol.40
, pp. 532-535
-
-
Neubert, K.1
Hartrodt, B.2
Mehlis, B.3
Ruger, M.4
Bergman, J.5
Lindau, J.6
Jakubke, H.D.7
Barth, A.8
-
33
-
-
9344271407
-
-
U. Ragnarsson, Ed., Almquist & Wiksell, Stockholm
-
G. Chassaing, S. Lavielle, O. Ploux, S. Julien, O. Convert, A. Marquet, J. C. Beaujouan, Y. Torrens and J. Glowinski in: Peptides 1984, U. Ragnarsson, Ed., p. 345-348, Almquist & Wiksell, Stockholm 1985.
-
(1985)
Peptides 1984
, pp. 345-348
-
-
Chassaing, G.1
Lavielle, S.2
Ploux, O.3
Julien, S.4
Convert, O.5
Marquet, A.6
Beaujouan, J.C.7
Torrens, Y.8
Glowinski, J.9
-
34
-
-
0022392659
-
Conformationally restricted C-terminal peptides of substance P. Synthesis, mass spectral analysis and pharmacological properties
-
D. Theodoropoulos, C. Poulos, D. Gatos, P. Cordopatis, E. Escher, J. Mizrahi, D. Regoli, D. Dalietos, A. Furst and T. D. Lee (1985). Conformationally restricted C-terminal peptides of substance P. Synthesis, mass spectral analysis and pharmacological properties. J. Med. Chem. 28, 1536-1539.
-
(1985)
J. Med. Chem.
, vol.28
, pp. 1536-1539
-
-
Theodoropoulos, D.1
Poulos, C.2
Gatos, D.3
Cordopatis, P.4
Escher, E.5
Mizrahi, J.6
Regoli, D.7
Dalietos, D.8
Furst, A.9
Lee, T.D.10
-
35
-
-
0022368711
-
Conformationally restricted cyclic analogues of substance P: Insight into the receptor binding process
-
P. S. Darman, G. C. Landis, J. R. Smits, L. D. Hirning, K. Gulya, H. I. Yamamura, T. F. Burks and V. J. Hruby (1985). Conformationally restricted cyclic analogues of substance P: Insight into the receptor binding process. Biochem. Biophys. Res. Commun. 127, 656-662.
-
(1985)
Biochem. Biophys. Res. Commun.
, vol.127
, pp. 656-662
-
-
Darman, P.S.1
Landis, G.C.2
Smits, J.R.3
Hirning, L.D.4
Gulya, K.5
Yamamura, H.I.6
Burks, T.F.7
Hruby, V.J.8
-
36
-
-
85033816693
-
Synthesis and biological activity of NK-1 selective, N-backbone cyclic analogues of the C-terminal hexapeptide of substance P
-
in press
-
G. Byk, D. Halle, I. Zeltser, G. Bitan, Z. Selinger and C. Gilon. Synthesis and biological activity of NK-1 selective, N-backbone cyclic analogues of the C-terminal hexapeptide of substance P. J. Med. Chem., in press
-
J. Med. Chem.
-
-
Byk, G.1
Halle, D.2
Zeltser, I.3
Bitan, G.4
Selinger, Z.5
Gilon, C.6
-
37
-
-
0026751476
-
Conformation of cyclic analogues of substance P: NMR and molecular dynamics in dimethyl sulfoxide
-
J. Saulitis, D. F. Mierke, G. Byk, C. Gilon and H. Kessler (1992). Conformation of cyclic analogues of substance P: NMR and molecular dynamics in dimethyl sulfoxide. J. Am. Chem. Soc. 114, 4818-4827.
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 4818-4827
-
-
Saulitis, J.1
Mierke, D.F.2
Byk, G.3
Gilon, C.4
Kessler, H.5
-
38
-
-
0028340334
-
Comparison of the conformation of active and nonactive backbone cyclic analogues of substance P as a tool to elucidate features of the bioactive conformation: NMR and molecular dynamics in DMSO and water
-
S. Golic Grdadolnik, D. Mierke, G. Byk, I. Zeltser, C. Gilon and H. Kessler (1994). Comparison of the conformation of active and nonactive backbone cyclic analogues of substance P as a tool to elucidate features of the bioactive conformation: NMR and molecular dynamics in DMSO and water. J. Med. Chem. 37, 2145-2152.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 2145-2152
-
-
Golic Grdadolnik, S.1
Mierke, D.2
Byk, G.3
Zeltser, I.4
Gilon, C.5
Kessler, H.6
-
39
-
-
0001362806
-
New backbone cyclic substance P analogues
-
G. Bitan, S. Behrens, B. Mathä, Y. Mashriki, M. Hanani, H. Kessler and C. Gilon (1995). New backbone cyclic substance P analogues. Lett. Peptide Sci. 2, 121-124.
-
(1995)
Lett. Peptide Sci.
, vol.2
, pp. 121-124
-
-
Bitan, G.1
Behrens, S.2
Mathä, B.3
Mashriki, Y.4
Hanani, M.5
Kessler, H.6
Gilon, C.7
-
40
-
-
0025938850
-
New reduced peptide bond substance P agonists and antagonists: Effects on smooth muscle contraction
-
S. Zacharia, W. J. Rossowski, N.-Y. Jiang, P. Hibas, A. Ertan and D. H. Coy (1991). New reduced peptide bond substance P agonists and antagonists: Effects on smooth muscle contraction. Eur. J. Pharmacol. 203, 353-357.
-
(1991)
Eur. J. Pharmacol.
, vol.203
, pp. 353-357
-
-
Zacharia, S.1
Rossowski, W.J.2
Jiang, N.-Y.3
Hibas, P.4
Ertan, A.5
Coy, D.H.6
-
41
-
-
0023257815
-
Structure-activity studies on the C-terminal hexapeptide of substance P with modifications at the glutaminyl and methionyl residues
-
C. Poulos, G. Stavropoulos, J. R. Brown and C. C. Jordan (1987). Structure-activity studies on the C-terminal hexapeptide of substance P with modifications at the glutaminyl and methionyl residues. J. Med. Chem. 30, 1512-1515.
-
(1987)
J. Med. Chem.
, vol.30
, pp. 1512-1515
-
-
Poulos, C.1
Stavropoulos, G.2
Brown, J.R.3
Jordan, C.C.4
-
42
-
-
0027092387
-
How do peptides interact with lipid membranes and how does this affect their biological activity?
-
R. Schwyzer (1992). How do peptides interact with lipid membranes and how does this affect their biological activity? Brazilian J. Med. Biol. Res. 25, 1077-1089.
-
(1992)
Brazilian J. Med. Biol. Res.
, vol.25
, pp. 1077-1089
-
-
Schwyzer, R.1
-
43
-
-
0026009253
-
Synthesis of a potent agonist of substance P by modifying the methionyl and glutaminyl residues of the C-terminal hexapeptide of substance P
-
K. Karagiannis, A. Manolopoulou, G. Stavropoulos, C. Poulos, C. C. Jordan and R. M. Hagan (1991). Synthesis of a potent agonist of substance P by modifying the methionyl and glutaminyl residues of the C-terminal hexapeptide of substance P. Int. J. Peptide Protein Res. 38, 350-356.
-
(1991)
Int. J. Peptide Protein Res.
, vol.38
, pp. 350-356
-
-
Karagiannis, K.1
Manolopoulou, A.2
Stavropoulos, G.3
Poulos, C.4
Jordan, C.C.5
Hagan, R.M.6
-
45
-
-
0029103012
-
Synthesis of peptide amides using Fmoc-based solid-phase procedures on 4-methyl-benzhydrylamine resins
-
P. E. Thompson, H. H. Keah, P. T. Gomme, P. G. Stanton and M. T. W. Hearn (1995). Synthesis of peptide amides using Fmoc-based solid-phase procedures on 4-methyl-benzhydrylamine resins. Int. J. Peptide Protein Res. 46, 174-180.
-
(1995)
Int. J. Peptide Protein Res.
, vol.46
, pp. 174-180
-
-
Thompson, P.E.1
Keah, H.H.2
Gomme, P.T.3
Stanton, P.G.4
Hearn, M.T.W.5
-
47
-
-
0000478940
-
General method for the rapid solid-phase synthesis of peptides: Specificity of antigen-antibody interaction at the level of individual amino acids
-
R. A. Houghten (1985). General method for the rapid solid-phase synthesis of peptides: Specificity of antigen-antibody interaction at the level of individual amino acids. Proc. Natl Acad. Sci. USA 82, 5131-5135.
-
(1985)
Proc. Natl Acad. Sci. USA
, vol.82
, pp. 5131-5135
-
-
Houghten, R.A.1
-
48
-
-
3042863884
-
-
C. H. Schneider and A. N. Eberle, Eds., ESCOM Science Publishers BV
-
S. Zimmer, E. Hoffmann, G. Jung and H. Kessler in: Peptides 1992, C. H. Schneider and A. N. Eberle, Eds., p. 393-394, ESCOM Science Publishers BV 1993.
-
(1993)
Peptides 1992
, pp. 393-394
-
-
Zimmer, S.1
Hoffmann, E.2
Jung, G.3
Kessler, H.4
|