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186 related items for PubMed ID: 9336327
1. The pharmacological characterization of a novel selective 5-hydroxytryptamine1A receptor antagonist, NAD-299. Johansson L, Sohn D, Thorberg SO, Jackson DM, Kelder D, Larsson LG, Rényi L, Ross SB, Wallsten C, Eriksson H, Hu PS, Jerning E, Mohell N, Westlind-Danielsson A. J Pharmacol Exp Ther; 1997 Oct; 283(1):216-25. PubMed ID: 9336327 [Abstract] [Full Text] [Related]
2. Characterization of the aminomethylchroman derivative BAY x 3702 as a highly potent 5-hydroxytryptamine1A receptor agonist. De Vry J, Schohe-Loop R, Heine HG, Greuel JM, Mauler F, Schmidt B, Sommermeyer H, Glaser T. J Pharmacol Exp Ther; 1998 Mar; 284(3):1082-94. PubMed ID: 9495870 [Abstract] [Full Text] [Related]
3. Electrophysiological comparison of 5-Hydroxytryptamine1A receptor antagonists on dorsal raphe cell firing. Martin LP, Jackson DM, Wallsten C, Waszczak BL. J Pharmacol Exp Ther; 1999 Feb; 288(2):820-6. PubMed ID: 9918594 [Abstract] [Full Text] [Related]
4. Facilitation and inhibition of male rat ejaculatory behaviour by the respective 5-HT1A and 5-HT1B receptor agonists 8-OH-DPAT and anpirtoline, as evidenced by use of the corresponding new and selective receptor antagonists NAD-299 and NAS-181. Hillegaart V, Ahlenius S. Br J Pharmacol; 1998 Dec; 125(8):1733-43. PubMed ID: 9886765 [Abstract] [Full Text] [Related]
5. The pharmacological profile of (R)-3,4-dihydro-N-isopropyl-3-(N-isopropyl-N-propylamino)-2H-1-benzopyran-5-carboxamide, a selective 5-hydroxytryptamine(1A) receptor agonist. Rënyi L, Evenden JL, Fowler CJ, Jerning E, Kelder D, Lake-Bakaar D, Larsson LG, Mohell N, Sällemark M, Ross SB. J Pharmacol Exp Ther; 2001 Dec; 299(3):883-93. PubMed ID: 11714872 [Abstract] [Full Text] [Related]
6. MP-3022, a new putative antagonist at pre- and postsynaptic 5-HT1A receptors. Przegaliński E, Filip M, Bijak M, Wedzony K, Budziszewska B, Tokarski K, Maćkowiak M, Fijał K. Pol J Pharmacol; 1996 Dec; 48(1):13-22. PubMed ID: 9112623 [Abstract] [Full Text] [Related]
7. S 14671: a naphtylpiperazine 5-hydroxytryptamine1A agonist of exceptional potency and high efficacy possessing antagonist activity at 5-hydroxytryptamine1C/2 receptors. Millan MJ, Rivet JM, Canton H, Lejeune F, Bervoets K, Brocco M, Gobert A, Lefebvre de Ladonchamps B, Le Marouille-Girardon S, Verriele L. J Pharmacol Exp Ther; 1992 Aug; 262(2):451-63. PubMed ID: 1323650 [Abstract] [Full Text] [Related]
8. Some pharmacological properties of new analogs of MP 3022, the 5-HT1A receptor antagonist. Chojnacka-Wójcik E, Kłodzińska A, Tatarczyńska E, Paluchowska MH. Pol J Pharmacol; 1999 Aug; 51(5):405-13. PubMed ID: 10817541 [Abstract] [Full Text] [Related]
9. Selective antiaggressive effects of alnespirone in resident-intruder test are mediated via 5-hydroxytryptamine1A receptors: A comparative pharmacological study with 8-hydroxy-2-dipropylaminotetralin, ipsapirone, buspirone, eltoprazine, and WAY-100635. de Boer SF, Lesourd M, Mocaer E, Koolhaas JM. J Pharmacol Exp Ther; 1999 Mar; 288(3):1125-33. PubMed ID: 10027850 [Abstract] [Full Text] [Related]
10. Novel benzodioxopiperazines acting as antagonists at postsynaptic 5-HT1A receptors and as agonists at 5-HT1A autoreceptors: a comparative pharmacological characterization with proposed 5-HT1A antagonists. Millan MJ, Canton H, Gobert A, Lejeune F, Rivet JM, Bervoets K, Brocco M, Widdowson P, Mennini T, Audinot V. J Pharmacol Exp Ther; 1994 Jan; 268(1):337-52. PubMed ID: 8301575 [Abstract] [Full Text] [Related]
11. Antagonist properties of (-)-pindolol and WAY 100635 at somatodendritic and postsynaptic 5-HT1A receptors in the rat brain. Corradetti R, Laaris N, Hanoun N, Laporte AM, Le Poul E, Hamon M, Lanfumey L. Br J Pharmacol; 1998 Feb; 123(3):449-62. PubMed ID: 9504386 [Abstract] [Full Text] [Related]
12. A comparative in vitro and in vivo pharmacological characterization of the novel dopamine D3 receptor antagonists (+)-S 14297, nafadotride, GR 103,691 and U 99194. Audinot V, Newman-Tancredi A, Gobert A, Rivet JM, Brocco M, Lejeune F, Gluck L, Desposte I, Bervoets K, Dekeyne A, Millan MJ. J Pharmacol Exp Ther; 1998 Oct; 287(1):187-97. PubMed ID: 9765337 [Abstract] [Full Text] [Related]
13. WAY-100635, a potent and selective 5-hydroxytryptamine1A antagonist, increases serotonergic neuronal activity in behaving cats: comparison with (S)-WAY-100135. Fornal CA, Metzler CW, Gallegos RA, Veasey SC, McCreary AC, Jacobs BL. J Pharmacol Exp Ther; 1996 Aug; 278(2):752-62. PubMed ID: 8768728 [Abstract] [Full Text] [Related]
14. The selective 5-hydroxytryptamine 1A antagonist, AZD7371 [3(R)-(N,N-dicyclobutylamino)-8-fluoro-3,4-dihydro-2H-1-benzopyran-5-carboxamide (R,R)-tartrate monohydrate] (robalzotan tartrate monohydrate), inhibits visceral pain-related visceromotor, but not autonomic cardiovascular, responses to colorectal distension in rats. Lindström E, Ravnefjord A, Brusberg M, Hjorth S, Larsson H, Martinez V. J Pharmacol Exp Ther; 2009 Jun; 329(3):1048-55. PubMed ID: 19325032 [Abstract] [Full Text] [Related]
15. Two selective 5-HT1A receptor antagonists, WAY-100 635 and NDL-249, stimulate locomotion in rats acclimatised to their environment and alter their behaviour: a behavioural analysis. Jackson DM, Wallsten CE, Jerning E, Hu PS, Deveney AM. Psychopharmacology (Berl); 1998 Oct; 139(4):300-10. PubMed ID: 9809851 [Abstract] [Full Text] [Related]
16. Pharmacology of the novel 5-hydroxytryptamine1A receptor antagonist (S)-5-fluoro-8-hydroxy-2-(dipropylamino)tetralin: inhibition of (R)-8-hydroxy-2-(dipropylamino)tetralin-induced effects. Björk L, Cornfield LJ, Nelson DL, Hillver SE, Andén NE, Lewander T, Hacksell U. J Pharmacol Exp Ther; 1991 Jul 01; 258(1):58-65. PubMed ID: 1830099 [Abstract] [Full Text] [Related]
17. Nad-299 antagonises 5-HT-stimulated and spiperone-inhibited [35S]GTPgammaS binding in cloned 5-HT1A receptors. Jerning E, Rosqvist S, Mohell N. J Recept Signal Transduct Res; 2002 Jul 01; 22(1-4):483-95. PubMed ID: 12503636 [Abstract] [Full Text] [Related]
18. Induction of hypothermia as a model of 5-hydroxytryptamine1A receptor-mediated activity in the rat: a pharmacological characterization of the actions of novel agonists and antagonists. Millan MJ, Rivet JM, Canton H, Le Marouille-Girardon S, Gobert A. J Pharmacol Exp Ther; 1993 Mar 01; 264(3):1364-76. PubMed ID: 8450471 [Abstract] [Full Text] [Related]
19. Receptor binding characteristics of [3H]NAD-299, a new selective 5-HT1A receptor antagonist. Jerning E, Svantesson GT, Mohell N. Eur J Pharmacol; 1998 Nov 06; 360(2-3):219-25. PubMed ID: 9851589 [Abstract] [Full Text] [Related]
20. Synthesis and structure-activity relationships of a new model of arylpiperazines. 1. 2-[[4-(o-methoxyphenyl)piperazin-1-yl]methyl]-1, 3-dioxoperhydroimidazo[1,5-alpha]pyridine: a selective 5-HT1A receptor agonist. López-Rodríguez ML, Rosado ML, Benhamú B, Morcillo MJ, Sanz AM, Orensanz L, Beneitez ME, Fuentes JA, Manzanares J. J Med Chem; 1996 Oct 25; 39(22):4439-50. PubMed ID: 8893838 [Abstract] [Full Text] [Related] Page: [Next] [New Search]