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240 related items for PubMed ID: 14730096
1. Synthesis, in vitro and in vivo 5-HT1A/5-HT2A serotonin receptor activity of new hybrid 1,2,3,4-tetrahydro-gamma-carbolines with 1-(2-methoxyphenyl)piperazine moiety. Boksa J, Charakchieva-Minol S, Duszyńska B, Bugno R, Kłodzińska A, Tatarczyńska E, Chojnacka-Wójcik E, Bojarski AJ. Pol J Pharmacol; 2003; 55(6):1013-9. PubMed ID: 14730096 [Abstract] [Full Text] [Related]
2. 2-H- and 2-acyl-9- [omega-[4-(2-methoxyphenyl)piperazinyl]-alkyl]-1,2,3,4-tetrahydro-beta-carbolines as ligands of 5-HT1A and 5-HT2A receptors. Boksa J, Mokrosz MJ, Charakchieva-Minol S, Tatarczyńska E, Kłodzińska A, Wesołowska A, Misztal S. Pol J Pharmacol; 2001; 53(5):501-8. PubMed ID: 11990069 [Abstract] [Full Text] [Related]
3. Novel 4-alkyl-1-arylpiperazines and 1,2,3,4-tetrahydroisoquinolines containing diphenylmethylamino or diphenylmethoxy fragment with differentiated 5-HT1A/5-HT2A/D2 receptor activity. Paluchowska MH, Mokrosz MJ, Charakchieva-Minol S, Duszyńska B, Kozioł A, Wesołowska A, Stachowicz K, Chojnacka-Wójcik E. Pol J Pharmacol; 2003; 55(4):543-52. PubMed ID: 14581712 [Abstract] [Full Text] [Related]
4. 9-substituted 1,2,3,4-tetrahydro-beta-carbolin-1-ones, new 5-HT1A and 5-HT2A receptor ligands. Mokrosz MJ, Boksa J, Charakchieva-Minol S, Wesołowska A, Borycz J. Pol J Pharmacol; 1999; 51(4):351-6. PubMed ID: 10540967 [Abstract] [Full Text] [Related]
5. New 4-[omega-(diarylmethylamino)alkyl]- and 4-[omega-(diarylmethoxy)alkyl]-1-arylpiperazines as selective 5-HT1A/5-HT2A receptor ligands with differentiated in vivo activity. Paluchowska MH, Charakchieva-Minol S, Tatarczyńska E, Kłodzińska A, Stachowicz K, Chojnacka-Wójcik E. Pol J Pharmacol; 2004; 56(6):743-54. PubMed ID: 15662087 [Abstract] [Full Text] [Related]
6. 1,4-Benzoxazin-3(4H)-one derivatives and related compounds as 5-HT1A and 5-HT2A receptor ligands; the effect of the terminal amide fragment on the 5-HT1A/5-HT2A affinity and functional activity. Mokrosz MJ, Kowalski P, Kowalska T, Majka Z, Duszyńska B, Charakchieva-Minol S, Szaro A, Tatarczyńska E, Kłodzińska A, Chojnacka-Wójcik E. Pol J Pharmacol; 1998; 50(4-5):333-40. PubMed ID: 10091718 [Abstract] [Full Text] [Related]
7. Synthesis, 5-HT1A and 5-HT2A receptor activity of new 1-phenylpiperazinylpropyl derivatives with arylalkyl substituents in position 7 of purine-2,6-dione. Chloń G, Pawłowski M, Duszyńska B, Szaro A, Tatarczńska E, Kłodzińska AL, Chojnacka-Wójcik E. Pol J Pharmacol; 2001; 53(4):359-68. PubMed ID: 11990082 [Abstract] [Full Text] [Related]
8. 1-Aryl-4-(4-succinimidobutyl)piperazines and their conformationally constrained analogues: synthesis, binding to serotonin (5-HT1A, 5-HT2A, 5-HT7), alpha1-adrenergic, and dopaminergic D2 receptors, and in vivo 5-HT1A functional characteristics. Bojarski AJ, Paluchowska MH, Duszyńska B, Kłodzińska A, Tatarczyńska E, Chojnacka-Wójcik E. Bioorg Med Chem; 2005 Mar 15; 13(6):2293-303. PubMed ID: 15727878 [Abstract] [Full Text] [Related]
9. Synthesis of new hexahydro- and octahydropyrido[1,2-c]pyrimidine derivatives with an arylpiperazine moiety as ligands for 5-HT1A and 5-HT2A receptors. Part 4. Herold F, Król M, Kleps J, Nowak G. Eur J Med Chem; 2006 Jan 15; 41(1):125-34. PubMed ID: 16263195 [Abstract] [Full Text] [Related]
10. Substitution mode of the amide fragment in some new N-[omega-[4-(2-methoxyphenyl)piperazin-1-yl]alkyl]pyrid-2(1H)-ones and their 5-HT1A/5-HT2A activity. Paluchowska MH, Bugno R, Charakchieva-Minol S, Bojarski AJ, Wesołowska A. Pol J Pharmacol; 2001 Jan 15; 53(4):369-76. PubMed ID: 11990083 [Abstract] [Full Text] [Related]
11. Effect of the amide fragment on 5-HT1A receptor activity of some analogs of MP 3022. Paluchowska MH, Charakchieva-Minol S, Tatarczyńska E, Kłodzińska A. Pol J Pharmacol; 1999 Jan 15; 51(5):415-21. PubMed ID: 10817542 [Abstract] [Full Text] [Related]
12. New arylpiperazine 5-HT(1A) receptor ligands containing the pyrimido[2,1-f]purine fragment: synthesis, in vitro, and in vivo pharmacological evaluation. Jurczyk S, Kołaczkowski M, Maryniak E, Zajdel P, Pawłowski M, Tatarczyńska E, Kłodzińska A, Chojnacka-Wójcik E, Bojarski AJ, Charakchieva-Minol S, Duszyńska B, Nowak G, Maciag D. J Med Chem; 2004 May 06; 47(10):2659-66. PubMed ID: 15115407 [Abstract] [Full Text] [Related]
13. Structure-activity relationship studies of CNS agents. Part 24: New analogs of N-tert.-butyl-3-[4-(2-methoxyphenyl)-1-piperazinyl]-2-phenylpropanamide (WAY-100135). Boksa J, Klodzińska A, Charakchieva-Minol S, Chojnacka-Wójcik E, Mokrosz JL. Pharmazie; 1996 Feb 06; 51(2):72-6. PubMed ID: 8720802 [Abstract] [Full Text] [Related]
14. Anxiolytic-like effect of a serotonergic ligand with high affinity for 5-HT1A, 5-HT2A and 5-HT3 receptors. Delgado M, Caicoya AG, Greciano V, Benhamú B, López-Rodríguez ML, Fernández-Alfonso MS, Pozo MA, Manzanares J, Fuentes JA. Eur J Pharmacol; 2005 Mar 21; 511(1):9-19. PubMed ID: 15777774 [Abstract] [Full Text] [Related]
15. Structure-affinity relationship study on N-(1,2,3,4-tetrahydronaphthalen-1-yl)-4-aryl-1-piperazinealkylamides, a new class of 5-hydroxytryptamine7 receptor agents. Leopoldo M, Berardi F, Colabufo NA, Contino M, Lacivita E, Niso M, Perrone R, Tortorella V. J Med Chem; 2004 Dec 16; 47(26):6616-24. PubMed ID: 15588097 [Abstract] [Full Text] [Related]
16. Influence of the aliphatic spacer length on the 5-HT1A receptor activity of new arylpiperazines with an indazole system. Paluchowska MH, Duszyńska B, Kłodzińska A, Tatarczyńska E. Pol J Pharmacol; 2000 Dec 16; 52(3):209-16. PubMed ID: 11055578 [Abstract] [Full Text] [Related]
17. Synthesis and 5-HT1A/5-HT2A receptor activity of new N-[3-(4-phenylpiperazin-1-yl)-propyl] derivatives of 3-spiro-cyclohexanepyrrolidine-2,5-dione and 3-spiro-beta-tetralonepyrrolidine-2,5-dione. Obniska J, Pawłowski M, Kołaczkowski M, Czopek A, Duszyńska B, Klodzińska A, Tatarczyńska E, Chojnacka-Wójcik E. Pol J Pharmacol; 2003 Dec 16; 55(4):553-7. PubMed ID: 14581713 [Abstract] [Full Text] [Related]
18. Synthesis and structure-activity relationships of a new model of arylpiperazines. 4. 1-[omega-(4-Arylpiperazin-1-yl)alkyl]-3-(diphenylmethylene) - 2, 5-pyrrolidinediones and -3-(9H-fluoren-9-ylidene)-2, 5-pyrrolidinediones: study of the steric requirements of the terminal amide fragment on 5-HT1A affinity/selectivity. López-Rodríguez ML, Morcillo MJ, Rovat TK, Fernández E, Vicente B, Sanz AM, Hernández M, Orensanz L. J Med Chem; 1999 Jan 14; 42(1):36-49. PubMed ID: 9888831 [Abstract] [Full Text] [Related]
19. Novel N-[omega-[4-(2-methoxyphenyl)piperazin-1-yl]-ethyl]pyrid-2(1H)-ones with diversified 5-HT1A receptor activity. Paluchowska MH, Bugno R, Charakchieva-Minol S, Wesołowska A, Chojnacka-Wójcik E. Pol J Pharmacol; 2002 Jan 14; 54(6):641-6. PubMed ID: 12866719 [Abstract] [Full Text] [Related]
20. New 5-hydroxytryptamine(1A) receptor ligands containing a norbornene nucleus: synthesis and in vitro pharmacological evaluation. Fiorino F, Perissutti E, Severino B, Santagada V, Cirillo D, Terracciano S, Massarelli P, Bruni G, Collavoli E, Renner C, Caliendo G. J Med Chem; 2005 Aug 25; 48(17):5495-503. PubMed ID: 16107148 [Abstract] [Full Text] [Related] Page: [Next] [New Search]