-
2
-
-
0032134722
-
5-HT1-like receptors: A time to bid goodbye
-
references therein
-
Saxena, P. R.; de Vries, P.; Villalon, C. M. 5-HT1-like Receptors: a Time to Bid Goodbye. Trends Pharmacol Sci. 1998, 19, 311-316 and references therein.
-
(1998)
Trends Pharmacol Sci.
, vol.19
, pp. 311-316
-
-
Saxena, P.R.1
De Vries, P.2
Villalon, C.M.3
-
3
-
-
0031014883
-
Physiology of chemotherapy-induced emesis and antiemetic therapy. Predictive models for evaluation of new compounds
-
Veyrat-Follet, C.; Farinotti, R.; Palmer, J. L. Physiology of Chemotherapy-Induced Emesis and Antiemetic Therapy. Predictive Models for Evaluation of New Compounds. Drugs 1997, 53, 206-234.
-
(1997)
Drugs
, vol.53
, pp. 206-234
-
-
Veyrat-Follet, C.1
Farinotti, R.2
Palmer, J.L.3
-
6
-
-
9844234810
-
3 receptor agonists based on a pyrroloquinoxaline structure
-
3 Receptor Agonists Based on a Pyrroloquinoxaline Structure. J. Med. Chem. 1997, 40, 3670-3678.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 3670-3678
-
-
Cappelli, A.1
Nacci, V.2
Anzini, M.3
Vomero, S.4
Hamon, M.5
Cagnotto, A.6
Fracasso, C.7
Uboldi, C.8
Caccia, S.9
Consolo, S.10
Mennini, T.11
-
7
-
-
0030937244
-
Organic fluorine hardly ever accepts hydrogen bonds
-
(b) Dunitz, J. D.; Tylor, R. Organic Fluorine Hardly Ever Accepts Hydrogen Bonds. Chemistry-A Eur. J. 1997, 3, 89-98.
-
(1997)
Chemistry-A Eur. J.
, vol.3
, pp. 89-98
-
-
J, D.1
Tylor, R.2
-
10
-
-
15844421030
-
3 receptors. Part 1. Synthesis and biological evaluation of piperazinopyrrolothienopyrazines
-
3 Receptors. Part 1. Synthesis and Biological Evaluation of Piperazinopyrrolothienopyrazines. J. Med. Chem. 1996, 39, 2068-2080.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 2068-2080
-
-
Rault, S.1
Lancelot, G.2
Prunier, H.3
Robba, M.4
Renard, P.5
Delagrange, P.6
Pfeiffer, B.7
Caignard, D.8
Guardiola-Lemaitre, B.9
Hamon, M.10
-
11
-
-
15644378822
-
3 receptors. 2. Synthesis and biological evaluation of piperazinopyridopyrrolopyrazines, piperazinopyrroloquinoxalines, and piperazinopyridopyrroloquinoxalines
-
3 Receptors. 2. Synthesis and Biological Evaluation of Piperazinopyridopyrrolopyrazines, Piperazinopyrroloquinoxalines, and Piperazinopyridopyrroloquinoxalines. J. Med. Chem. 1997, 40, 1808-1819.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 1808-1819
-
-
Prunier, H.1
Rault, S.2
Lancelot, J.-C.3
Robba, M.4
Renard, P.5
Delagrange, P.6
Pfeiffer, B.7
Caignard, D.-H.8
Misslin, R.9
Guardiola-Lemaitre, B.10
Hamon, M.11
-
12
-
-
0025947401
-
Novel compounds possessing potent cAMP and cGMP phosphodiesterase inhibitory activity. Synthesis and cardiovascular effects of a series of imidazo[1,2-a]quinoxalinones and imidazo[1,5-a]quinoxalinones, and their aza analogues
-
(a) Davey, D. D.; Erhardt, P. W.; Cantoe, E. H.; Greenberg, S. S.; Ingebretsen, W. R.; Wiggins, J. Novel Compounds Possessing potent cAMP and cGMP Phosphodiesterase Inhibitory Activity. Synthesis and Cardiovascular Effects of a Series of Imidazo[1,2-a]quinoxalinones and Imidazo[1,5-a]quinoxalinones, and Their Aza Analogues. J. Med. Chem. 1991, 34, 2671-2677.
-
(1991)
J. Med. Chem.
, vol.34
, pp. 2671-2677
-
-
Davey, D.D.1
Erhardt, P.W.2
Cantoe, E.H.3
Greenberg, S.S.4
Ingebretsen, W.R.5
Wiggins, J.6
-
13
-
-
0344099697
-
-
U.S. Patent 4,112,098, Sept 5, 1978, Appl. 842,718, Oct 17
-
(b) Vogt, B. R. U.S. Patent 4,112,098, Sept 5, 1978, Appl. 842,718, Oct 17, 1977; Chem. Abstr. 1979, 90, 137848k.
-
(1977)
-
-
Vogt, B.R.1
-
14
-
-
24844481223
-
-
(b) Vogt, B. R. U.S. Patent 4,112,098, Sept 5, 1978, Appl. 842,718, Oct 17, 1977; Chem. Abstr. 1979, 90, 137848k.
-
(1979)
Chem. Abstr.
, vol.90
-
-
-
15
-
-
0344961987
-
-
Japanese Patent 74 27,877, July 22, 1974, Appl. 70 129,461, Dec 30
-
Akira, M.; Watanabe, T. Japanese Patent 74 27,877, July 22, 1974, Appl. 70 129,461, Dec 30, 1970; Chem. Abstr. 1975, 82, 156398q.
-
(1970)
-
-
Akira, M.1
Watanabe, T.2
-
16
-
-
85023549687
-
-
Akira, M.; Watanabe, T. Japanese Patent 74 27,877, July 22, 1974, Appl. 70 129,461, Dec 30, 1970; Chem. Abstr. 1975, 82, 156398q.
-
(1975)
Chem. Abstr.
, vol.82
-
-
-
17
-
-
0025861997
-
Polycondensed heterocycles. VII. A convenient synthesis of pyrrolo[1,2-a]-quinoxaline derivatives by intramolecular aromatic nucleophilic displacement
-
(a) Campiani, G.; Nacci, V.; Corelli, F.; Anzini, M. Polycondensed Heterocycles. VII. A Convenient Synthesis of Pyrrolo[1,2-a]-quinoxaline Derivatives by Intramolecular Aromatic Nucleophilic Displacement. Synth. Commun. 1991, 21, 1567-1576.
-
(1991)
Synth. Commun.
, vol.21
, pp. 1567-1576
-
-
Campiani, G.1
Nacci, V.2
Corelli, F.3
Anzini, M.4
-
18
-
-
0001826836
-
Alkylthiophenes as versatile synthetic precursor. Part I. A new route to 3-thienyl aldehydes and ketones
-
(b) 2-(Bromomethyl)thiophene, 2-(bromomethyl)furan, 2-bromo-5-(bromomethyl)thiophene, and 2-bromo-5-(bromomethyl)furan were prepared according to the following reference: Clarke, J. A.; Meth-Cohn, O. Alkylthiophenes as Versatile Synthetic Precursor. Part I. A New Route to 3-Thienyl Aldehydes and Ketones. Tetrahedron Lett. 1975, 52, 4705-4708.
-
(1975)
Tetrahedron Lett.
, vol.52
, pp. 4705-4708
-
-
Clarke, J.A.1
Meth-Cohn, O.2
-
19
-
-
0020661061
-
Piperazinylimidazo[1,2-a]pyrazines with selective affinity for in vitro α-adrenergic receptor subtypes
-
(a) Lumma, W. C.; Randall, W. C.; Cresson, E. L.; Huff, G. R.; Hartman, R. D.; Lyon, T. F. Piperazinylimidazo[1,2-a]pyrazines with Selective Affinity for In Vitro α-Adrenergic Receptor Subtypes. J. Med. Chem. 1983, 26, 357-363.
-
(1983)
J. Med. Chem.
, vol.26
, pp. 357-363
-
-
Lumma, W.C.1
Randall, W.C.2
Cresson, E.L.3
Huff, G.R.4
Hartman, R.D.5
Lyon, T.F.6
-
20
-
-
0024321953
-
An unexpected aminolysis in the synthesis of 5-substituted 3-(1H-Tetrazol-5-yl)pyrazolo[1,5-a]quinazolines
-
(b) Norton, P. P. An Unexpected Aminolysis in the Synthesis of 5-Substituted 3-(1H-Tetrazol-5-yl)pyrazolo[1,5-a]quinazolines. J. Heterocycl. Chem. 1989, 26, 713-716.
-
(1989)
J. Heterocycl. Chem.
, vol.26
, pp. 713-716
-
-
Norton, P.P.1
-
21
-
-
0018001339
-
Simultaneous analysis of families of sigmoidal curves: Application to bioassay, radioligand assay, and physiological dose-response curves
-
(a) De Lean, K. W.; Munson, P. J.; Rodbard, D. Simultaneous Analysis of Families of Sigmoidal Curves: Application to Bioassay, Radioligand Assay, and Physiological Dose-Response Curves. Am. J. Physiol. 1978, 235, E97-E102.
-
(1978)
Am. J. Physiol.
, vol.235
-
-
De Lean, K.W.1
Munson, P.J.2
Rodbard, D.3
-
22
-
-
0033559918
-
Hydrogen bonding, hydrophobic interactions, and failure of the rigid receptor hypothesis
-
(b) Davis, A. M.; Teague, S. J. Hydrogen Bonding, Hydrophobic Interactions, and Failure of the Rigid Receptor Hypothesis. Angew. Chem., Int. Ed. 1999, 38, 736-749.
-
(1999)
Angew. Chem., Int. Ed.
, vol.38
, pp. 736-749
-
-
Davis, A.M.1
Teague, S.J.2
-
23
-
-
0025194186
-
3 binding sites in the rat cerebral cortex and NG108-15 clonal cells
-
3 Binding Sites in the Rat Cerebral Cortex and NG108-15 Clonal Cells. Biochem. Pharmacol. 1990, 40, 1541-1550.
-
(1990)
Biochem. Pharmacol.
, vol.40
, pp. 1541-1550
-
-
Bolanos, F.J.1
Schechter, L.E.2
Miquel, M.C.3
Emerit, M.B.4
Rumigny, J.F.5
Hamon, M.6
Gozlan, H.7
-
24
-
-
0019199013
-
Preliminary report of a simple animal behavior model for the anxiolytic effects of benzodiazepines
-
Crawley, J. N.; Goodwin, F. K. Preliminary Report of a Simple Animal Behavior Model for the Anxiolytic Effects of Benzodiazepines. Pharmacol. Biochem. Behav. 1980,13, 167-170.
-
(1980)
Pharmacol. Biochem. Behav.
, vol.13
, pp. 167-170
-
-
Crawley, J.N.1
Goodwin, F.K.2
-
25
-
-
0019823545
-
Neuropharmacology specificity of a simple animal model for the behavioral actions of benzodiazepines
-
Crawley, J. N. Neuropharmacology Specificity of a Simple Animal Model for the Behavioral Actions of Benzodiazepines. Pharmacol. Biochem. Behav. 1981, 15, 695-699.
-
(1981)
Pharmacol. Biochem. Behav.
, vol.15
, pp. 695-699
-
-
Crawley, J.N.1
-
26
-
-
0023875045
-
3 receptor antagonist
-
3 Receptor Antagonist. Br. J. Pharmacol. 1988, 93, 985-993.
-
(1988)
Br. J. Pharmacol.
, vol.93
, pp. 985-993
-
-
Jones, B.J.1
Costall, B.2
Domeney, A.M.3
Kelly, M.E.4
Naylor, R.J.5
Oakley, N.R.6
Tyers, M.B.7
-
27
-
-
0024324557
-
Exploration of mice in a black and white test box: Validation as a model of anxiety
-
Costall, B.; Jones, B. J.; Kelly, M. E.; Naylor, R. J.; Tomkins, D. M. Exploration of Mice in a Black and White Test Box: Validation as a Model of Anxiety. Pharmacol. Biochem. Behav. 1989, 32, 777-785.
-
(1989)
Pharmacol. Biochem. Behav.
, vol.32
, pp. 777-785
-
-
Costall, B.1
Jones, B.J.2
Kelly, M.E.3
Naylor, R.J.4
Tomkins, D.M.5
-
30
-
-
0025925108
-
3 receptor-mediated antinociception: Possible release of GABA
-
3 Receptor-mediated Antinociception: Possible Release of GABA. J. Neurosci. 1991, 11, 1881-1888.
-
(1991)
J. Neurosci.
, vol.11
, pp. 1881-1888
-
-
Alhaider, A.A.1
Lei, S.Z.2
Wilcox, G.L.3
-
31
-
-
0025225393
-
1-Arylpiperazines as active metabolites of (4-Substituted Aryl-1-piperazinyl)alkyl heterocyclic drugs
-
(a) Caccia, S.; Garattini, S. 1-Arylpiperazines as Active Metabolites of (4-Substituted Aryl-1-piperazinyl)alkyl Heterocyclic Drugs. Acta Pharmacol. Yugosl. 1990, 40, 441-460.
-
(1990)
Acta Pharmacol. Yugosl.
, vol.40
, pp. 441-460
-
-
Caccia, S.1
Garattini, S.2
-
32
-
-
0344531115
-
-
note
-
(b) The n-octanol/ water log P values of compounds 20b,l,u,v,ee were calculated using the ClogP program, version 2.0, Biobyte Corp. (Claremont, CA).
-
-
-
-
33
-
-
0029052166
-
3 receptor antagonists based on the arylpiperazine skeleton: Synthesis, structure, biological activity, and comparative molecular field analysis studies
-
3 Receptor Antagonists Based on the Arylpiperazine Skeleton: Synthesis, Structure, Biological Activity, and Comparative Molecular Field Analysis Studies. J. Med. Chem. 1995, 38, 2692-2704.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 2692-2704
-
-
Anzini, M.1
Cappelli, A.2
Vomero, S.3
Giorgi, G.4
Langer, T.5
Hamon, M.6
Merahi, N.7
Emerit, B.M.8
Cagnotte, A.9
Skorupska, M.10
Mennini, T.11
Pinto, J.C.12
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