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Volumn 49, Issue 13, 2006, Pages 3938-3947

2-[(4-Phenylpiperazin-1-yl)methyl]imidazo(di)azines as selective D 4-ligands. Induction of penile erection by 2-[4-(2-methoxyphenyl) piperazin-1-ylmethyl]imidazo[1,2-a]pyridine (PIP3EA), a potent and selective D4 partial agonist

Author keywords

[No Author keywords available]

Indexed keywords

2 [(4 PHENYLPIPERAZIL 1 YL)METHYL]IMIDAZO(DI)AZINE DERIVATIVE; 2 [4 (2 METHOXYPHENYL)PIPERAZIN 1 YLMETHYL]IMIDAZO[1,2 A]PYRIDINE; 2 DIPROPYLAMINO 8 HYDROXYTETRALIN; 3 [[4 (4 CHLOROPHENYL) 1 PIPERAZINYL]METHYL] 1H PYRROLO[2,3 B]PYRIDINE; 8 CHLORO 2,3,4,5 TETRAHYDRO 3 METHYL 5 PHENYL 1H 3 BENZAZEPIN 7 OL HYDROGEN MALEATE; A 412997; A 419227; ABT 724; CLOZAPINE; CP 226269; DOPAMINE 4 RECEPTOR; DOPAMINE 4 RECEPTOR ANTAGONIST; DOPAMINE RECEPTOR AFFECTING AGENT; DOPAMINE RECEPTOR BLOCKING AGENT; FAUC 113; FAUC 299; FAUC 319; GUANOSINE 5' O (3 THIOTRIPHOSPHATE); HALOPERIDOL; IMIDAZO[1,2 A]PYRIDINE DERIVATIVE; KETANSERIN; PARTIAL AGONIST; PD 168077; PD 186077; PRAZOSIN; QUINPIROLE; SPIPERONE; UNCLASSIFIED DRUG;

EID: 33745659402     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm060166w     Document Type: Article
Times cited : (68)

References (52)
  • 2
    • 0030969584 scopus 로고    scopus 로고
    • Dopamine receptor diversity: Molecular and pharmacological perspectives
    • Hartman, D. S.; Civelli, O. Dopamine receptor diversity: molecular and pharmacological perspectives. Prog. Drug Res. 1997, 48, 173-194.
    • (1997) Prog. Drug Res. , vol.48 , pp. 173-194
    • Hartman, D.S.1    Civelli, O.2
  • 4
    • 0033915001 scopus 로고    scopus 로고
    • 4 receptor a controversial therapeutic target
    • 4 receptor a controversial therapeutic target. Drugs Future 2000, 25, 587-611.
    • (2000) Drugs Future , vol.25 , pp. 587-611
    • Hrib, N.J.1
  • 9
    • 1842628624 scopus 로고    scopus 로고
    • 4 ligands and models of receptor activation: 2-(4-pyridin-2-ylpiperazin-1-ylmethyl)-1H-benzimidazole and related heteroarylmethylarylpiperazines exhibit a substituent effect responsible for additional efficacy tuning
    • 4 ligands and models of receptor activation: 2-(4-pyridin-2-ylpiperazin-1-ylmethyl)-1H-benzimidazole and related heteroarylmethylarylpiperazines exhibit a substituent effect responsible for additional efficacy tuning. J. Med. Chem. 2004, 47, 2348-2355.
    • (2004) J. Med. Chem. , vol.47 , pp. 2348-2355
    • Stewart, A.O.1    Cowart, M.D.2    Moreland, R.B.3    Latshaw, S.P.4    Matulenko, M.A.5
  • 13
    • 16244369423 scopus 로고    scopus 로고
    • 4 receptor agonist, induces penile erection when injected into the paraventricular nucleus of male rats
    • 4 receptor agonist, induces penile erection when injected into the paraventricular nucleus of male rats. Neurosci. Lett. 2005, 379, 59-62.
    • (2005) Neurosci. Lett. , vol.379 , pp. 59-62
    • Melis, M.R.1    Succu, S.2    Mascia, M.S.3    Argiolas, A.4
  • 14
    • 9144229084 scopus 로고    scopus 로고
    • Central mechanisms regulating penile erection in conscious rats: The dopaminergic systems related to the proerectile effect of apomorphine
    • Hsieh, G. C.; Hollingsworth, P. R.; Martino, B.; Chang, R.; Terranova, M. A.; et al. Central mechanisms regulating penile erection in conscious rats: the dopaminergic systems related to the proerectile effect of apomorphine. J. Pharmacol. Exp. Ther. 2004, 308, 330-338.
    • (2004) J. Pharmacol. Exp. Ther. , vol.308 , pp. 330-338
    • Hsieh, G.C.1    Hollingsworth, P.R.2    Martino, B.3    Chang, R.4    Terranova, M.A.5
  • 16
    • 27744452422 scopus 로고    scopus 로고
    • 2-like receptor agonists accelerate barrier repair and inhibit the epidermal hyperplasia induced by barrier disruption
    • 2-like receptor agonists accelerate barrier repair and inhibit the epidermal hyperplasia induced by barrier disruption. J. Invest. Dermatol. 2005, 125, 783-789.
    • (2005) J. Invest. Dermatol. , vol.125 , pp. 783-789
    • Fuziwara, S.1    Suzuki, A.2    Inoue, K.3    Denda, M.4
  • 19
    • 0032922157 scopus 로고    scopus 로고
    • 4 receptor: Synthesis, ligand binding studies and comparison of molecular electrostatic potential maps
    • 4 receptor: synthesis, ligand binding studies and comparison of molecular electrostatic potential maps. Bioorg. Med. Chem. Lett. 1999, 9, 97-102.
    • (1999) Bioorg. Med. Chem. Lett. , vol.9 , pp. 97-102
    • Lober, S.1    Hubner, H.2    Gmeiner, P.3
  • 20
    • 0034676321 scopus 로고    scopus 로고
    • 4 receptor partial agonists: Solid-phase synthesis, binding assays, and functional experiments
    • 4 receptor partial agonists: solid-phase synthesis, binding assays, and functional experiments. J. Med. Chem. 2000, 43, 4563-4569.
    • (2000) J. Med. Chem. , vol.43 , pp. 4563-4569
    • Hubner, H.1    Kraxner, J.2    Gmeiner, P.3
  • 21
    • 0035899181 scopus 로고    scopus 로고
    • 4 receptor ligands leading to the complete antagonist 2-[4-(4-chlorophenyl) piperazin-1-ylmethyl]pyrazolo[1,5-a]pyridine (FAUC 213)
    • 4 receptor ligands leading to the complete antagonist 2-[4-(4-chlorophenyl)piperazin-1-ylmethyl]pyrazolo[1,5-a] pyridine (FAUC 213). J. Med. Chem. 2001, 44, 2691-2694.
    • (2001) J. Med. Chem. , vol.44 , pp. 2691-2694
    • Lober, S.1    Hubner, H.2    Utz, W.3    Gmeiner, P.4
  • 22
    • 4544276200 scopus 로고    scopus 로고
    • Phenylpiperazinylmethylheterocycle derivatives: Synthesis and dopamine receptor binding profiles
    • Abadi, A. H. Phenylpiperazinylmethylheterocycle derivatives: synthesis and dopamine receptor binding profiles. Arch. Pharm. (Weinheim, Ger.) 2004, 337, 383-390.
    • (2004) Arch. Pharm. (Weinheim, Ger.) , vol.337 , pp. 383-390
    • Abadi, A.H.1
  • 23
    • 0000891746 scopus 로고
    • Synthesis of pyridazine derivatives-VIII: Imidazo[1, 2-b]pyridazines and some tricyclic aza analogs
    • Stanovnik, B.; Tisler, M. Synthesis of pyridazine derivatives-VIII: imidazo[1, 2-b]pyridazines and some tricyclic aza analogs. Tetrahedron 1967, 23, 387-395.
    • (1967) Tetrahedron , vol.23 , pp. 387-395
    • Stanovnik, B.1    Tisler, M.2
  • 24
    • 0008587734 scopus 로고    scopus 로고
    • Imidazo[1,2-b]pyridazines - XXII - Synthesis of some 2-aryl-3-methoxy-6- (pyridinylmethylthio and pyridinylmethylamino)imidazo[1,2-b]pyridazines and their interactions with central and mitochondrial (peripheral-type) benzodiazepine receptors
    • Barlin, G. B.; Davies, L. P.; Ireland, S. J.; Ngu-Schwemlein, M. M. L. Imidazo[1,2-b]pyridazines - XXII - Synthesis of some 2-aryl-3-methoxy-6- (pyridinylmethylthio and pyridinylmethylamino)imidazo[1,2-b]pyridazines and their interactions with central and mitochondrial (peripheral-type) benzodiazepine receptors. Aust. J. Chem. 1997, 50, 91-95.
    • (1997) Aust. J. Chem. , vol.50 , pp. 91-95
    • Barlin, G.B.1    Davies, L.P.2    Ireland, S.J.3    Ngu-Schwemlein, M.M.L.4
  • 25
    • 0035695091 scopus 로고    scopus 로고
    • (Hetero)arylation of 6-halogenoimidazo[1,2-a]pyridines differently substituted at C(2): Influence of the 2-substituent on the Suzuki cross-coupling reaction
    • Enguehard, C.; Hervet, M.; Thery, I.; Renou, J. L.; Fauvelle, F.; et al. (Hetero)arylation of 6-halogenoimidazo[1,2-a]pyridines differently substituted at C(2): Influence of the 2-substituent on the Suzuki cross-coupling reaction. Helv. Chim. Acta 2001, 84, 3610-3614.
    • (2001) Helv. Chim. Acta , vol.84 , pp. 3610-3614
    • Enguehard, C.1    Hervet, M.2    Thery, I.3    Renou, J.L.4    Fauvelle, F.5
  • 26
    • 0242611987 scopus 로고    scopus 로고
    • Comparative study on the reactivity of 6-haloimidazo[1,2-a]pyridine derivatives towards Negishi- and Stille-coupling reactions
    • Hervet, M.; Thery, I.; Gueiffier, A.; Enguehard-Gueiffier, C. Comparative study on the reactivity of 6-haloimidazo[1,2-a]pyridine derivatives towards Negishi- and Stille-coupling reactions. Helv. Chim. Acta 2003, 86, 3461-3469.
    • (2003) Helv. Chim. Acta , vol.86 , pp. 3461-3469
    • Hervet, M.1    Thery, I.2    Gueiffier, A.3    Enguehard-Gueiffier, C.4
  • 27
    • 0037433554 scopus 로고    scopus 로고
    • Copper-catalyzed domino halide exchange-cyanation of aryl bromides
    • Zanon, J.; Klapars, A.; Buchwald, S. L. Copper-catalyzed domino halide exchange-cyanation of aryl bromides. J. Am. Chem. Soc. 2003, 125, 2890-2891.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 2890-2891
    • Zanon, J.1    Klapars, A.2    Buchwald, S.L.3
  • 28
    • 0038701001 scopus 로고    scopus 로고
    • Easy access to novel substituted 6-aminoimidazo[1,2-a]pyridines using palladium- and copper-catalyzed aminations
    • Enguehard, C.; Allouchi, H.; Gueiffier, A.; Buchwald, S. L. Easy access to novel substituted 6-aminoimidazo[1,2-a]pyridines using palladium- and copper-catalyzed aminations. J. Org. Chem. 2003, 68, 4367-4370.
    • (2003) J. Org. Chem. , vol.68 , pp. 4367-4370
    • Enguehard, C.1    Allouchi, H.2    Gueiffier, A.3    Buchwald, S.L.4
  • 29
    • 33745669984 scopus 로고    scopus 로고
    • From the particular reactivity of 8-halogenoimidazo[1,2-a]pyridine towards copper and palladium catalyzed aminations
    • Kazock, J.-Y.; Enguehard-Gueiffier, C.; Thery, I.; Gueiffier, A. From the particular reactivity of 8-halogenoimidazo[1,2-a]pyridine towards copper and palladium catalyzed aminations. Bull. Chem. Soc. Jpn. 2006, 79, 775-779.
    • (2006) Bull. Chem. Soc. Jpn. , vol.79 , pp. 775-779
    • Kazock, J.-Y.1    Enguehard-Gueiffier, C.2    Thery, I.3    Gueiffier, A.4
  • 30
    • 0037009958 scopus 로고    scopus 로고
    • The copper-catalyzed N-arylation of indoles
    • Antilla, J. C.; Klapars, A.; Buchwald, S. L. The copper-catalyzed N-arylation of indoles. J. Am. Chem. Soc. 2002, 124, 11684-11688.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 11684-11688
    • Antilla, J.C.1    Klapars, A.2    Buchwald, S.L.3
  • 31
    • 4143104684 scopus 로고    scopus 로고
    • Copper-diamine-catalyzed N-arylation of pyrroles, pyrazoles, indazoles, imidazoles, and triazoles
    • Antilla, J. C.; Baskin, J. M.; Barder, T. E.; Buchwald, S. L. Copper-diamine-catalyzed N-arylation of pyrroles, pyrazoles, indazoles, imidazoles, and triazoles. J. Org. Chem. 2004, 69, 5578-5587.
    • (2004) J. Org. Chem. , vol.69 , pp. 5578-5587
    • Antilla, J.C.1    Baskin, J.M.2    Barder, T.E.3    Buchwald, S.L.4
  • 32
    • 0038676266 scopus 로고    scopus 로고
    • Ipso- or erne-substitutions of 6-haloimidazo[1,2-a]pyridine derivatives with different azoles depending on the reaction conditions
    • Enguehard, C.; Allouchi, H.; Gueiffier, A.; Buchwald, S. L. Ipso- or erne-substitutions of 6-haloimidazo[1,2-a]pyridine derivatives with different azoles depending on the reaction conditions. J. Org. Chem. 2003, 68, 5614-5617.
    • (2003) J. Org. Chem. , vol.68 , pp. 5614-5617
    • Enguehard, C.1    Allouchi, H.2    Gueiffier, A.3    Buchwald, S.L.4
  • 33
    • 13444310501 scopus 로고    scopus 로고
    • Evaluation of the 2-substituent effect on the reactivity of the 8-haloimidazo[1,2-a]pyridine series towards Suzuki-type cross-coupling reaction
    • Kazock, J.-Y.; Enguehard-Gueiffier, C.; Thery, I.; Gueiffier, A. Evaluation of the 2-substituent effect on the reactivity of the 8-haloimidazo[1,2-a]pyridine series towards Suzuki-type cross-coupling reaction. Bull. Chem. Soc. Jpn. 2005, 78, 154-159.
    • (2005) Bull. Chem. Soc. Jpn. , vol.78 , pp. 154-159
    • Kazock, J.-Y.1    Enguehard-Gueiffier, C.2    Thery, I.3    Gueiffier, A.4
  • 43
    • 22744447482 scopus 로고    scopus 로고
    • Central control of penile erection: Role of the paraventricular nucleus of the hypothalamus
    • Argiolas, A.; Melis, M. R. Central control of penile erection: role of the paraventricular nucleus of the hypothalamus. Prog. Neurobiol. (Oxford) 2005, 76, 1-21.
    • (2005) Prog. Neurobiol. (Oxford) , vol.76 , pp. 1-21
    • Argiolas, A.1    Melis, M.R.2
  • 45
    • 0036184710 scopus 로고    scopus 로고
    • Synthesis of 2-substituted-3-nitroimidazo[1,2-b]pyridazines as potential biologically active agents
    • Terme, T.; Galtier, C.; Maldonado, J.; Crozet, M. P.; Gueiffier, A.; et al. Synthesis of 2-substituted-3-nitroimidazo[1,2-b]pyridazines as potential biologically active agents. J. Heterocycl. Chem. 2002, 39, 173-177.
    • (2002) J. Heterocycl. Chem. , vol.39 , pp. 173-177
    • Terme, T.1    Galtier, C.2    Maldonado, J.3    Crozet, M.P.4    Gueiffier, A.5
  • 46
    • 0021367032 scopus 로고
    • Synthesis of imidazo[1,2-a]pyrazine derivatives with uterine-relaxing, antibronchospastic, and cardiac-stimulating properties
    • Sablayrolles, C.; Cros, G. H.; Milhavet, J. C.; Rechenq, E.; Chapat, J. P.; et al. Synthesis of imidazo[1,2-a]pyrazine derivatives with uterine-relaxing, antibronchospastic, and cardiac-stimulating properties. J. Med. Chem. 1984, 27, 206-212.
    • (1984) J. Med. Chem. , vol.27 , pp. 206-212
    • Sablayrolles, C.1    Cros, G.H.2    Milhavet, J.C.3    Rechenq, E.4    Chapat, J.P.5
  • 50
    • 0023274568 scopus 로고
    • Apomorphine-induced penile erection and yawning: Site of action in brain
    • Melis, M. R.; Argiolas, A.; Gessa, G. L. Apomorphine-induced penile erection and yawning: site of action in brain. Brain Res. 1987, 415, 98-104.
    • (1987) Brain Res. , vol.415 , pp. 98-104
    • Melis, M.R.1    Argiolas, A.2    Gessa, G.L.3


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