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PUBMED FOR HANDHELDS

Journal Abstract Search


166 related items for PubMed ID: 23141912

  • 21. The multiobjective based design, synthesis and evaluation of the arylsulfonamide/amide derivatives of aryloxyethyl- and arylthioethyl- piperidines and pyrrolidines as a novel class of potent 5-HT₇ receptor antagonists.
    Zajdel P, Kurczab R, Grychowska K, Satała G, Pawłowski M, Bojarski AJ.
    Eur J Med Chem; 2012 Oct; 56():348-60. PubMed ID: 22926225
    [Abstract] [Full Text] [Related]

  • 22. Isoindol-1-one analogues of 4-(2'-methoxyphenyl)-1-[2'-[N-(2"-pyridyl)-p-iodobenzamido]ethyl]pipera zine (p-MPPI) as 5-HT1A receptor ligands.
    Zhuang ZP, Kung MP, Mu M, Kung HF.
    J Med Chem; 1998 Jan 15; 41(2):157-66. PubMed ID: 9457239
    [Abstract] [Full Text] [Related]

  • 23. Synthesis of new serotonin 5-HT7 receptor ligands. Determinants of 5-HT7/5-HT1A receptor selectivity.
    Medina RA, Sallander J, Benhamú B, Porras E, Campillo M, Pardo L, López-Rodríguez ML.
    J Med Chem; 2009 Apr 23; 52(8):2384-92. PubMed ID: 19326916
    [Abstract] [Full Text] [Related]

  • 24. Synthesis and in vitro Evaluation of Novel Indole-Based Sigma Receptors Ligands.
    Yarim M, Koksal M, Schepmann D, Wünsch B.
    Chem Biol Drug Des; 2011 Nov 23; 78(5):869-75. PubMed ID: 21848665
    [Abstract] [Full Text] [Related]

  • 25. Design, synthesis and preliminary screening of novel 3-(2-N,N-dimethylaminoethylthio) indole derivatives as potential 5-HT(6) receptor ligands.
    Kambhampati R, Konda J, Reballi V, Shinde AK, Dubey PK, Nirogi RV.
    J Enzyme Inhib Med Chem; 2008 Jun 23; 23(3):302-12. PubMed ID: 18569332
    [Abstract] [Full Text] [Related]

  • 26. Epiminocyclohepta[b]indole analogs as 5-HT6 antagonists.
    Henderson AJ, Guzzo PR, Ghosh A, Kaur J, Koo JM, Nacro K, Panduga S, Pathak R, Shimpukade B, Tan V, Xiang K, Wierschke JD, Isherwood ML.
    Bioorg Med Chem Lett; 2012 Feb 15; 22(4):1494-8. PubMed ID: 22290076
    [Abstract] [Full Text] [Related]

  • 27. Synthesis, docking and pharmacological evaluation of novel homo- and hetero-bis 3-piperazinylpropylindole derivatives at SERT and 5-HT1A receptor.
    Pessoa-Mahana H, González-Lira C, Fierro A, Zapata-Torres G, Pessoa-Mahana CD, Ortiz-Severin J, Iturriaga-Vásquez P, Reyes-Parada M, Silva-Matus P, Saitz-Barría C, Araya-Maturana R.
    Bioorg Med Chem; 2013 Dec 15; 21(24):7604-11. PubMed ID: 24262884
    [Abstract] [Full Text] [Related]

  • 28. Design and synthesis of novel series of 5-HT6 receptor ligands having indole, a central aromatic core and 1-amino-4 methyl piperazine as a positive ionizable group.
    Hayat F, Cho S, Rhim H, Indu Viswanath AN, Pae AN, Lee JY, Choo DJ, Choo HY.
    Bioorg Med Chem; 2013 Sep 01; 21(17):5573-82. PubMed ID: 23810425
    [Abstract] [Full Text] [Related]

  • 29. Synthesis and serotonergic activity of substituted 2, N-benzylcarboxamido-5-(2-ethyl-1-dioxoimidazolidinyl)-N, N-dimethyltryptamine derivatives: novel antagonists for the vascular 5-HT(1B)-like receptor.
    Moloney GP, Martin GR, Mathews N, Milne A, Hobbs H, Dodsworth S, Sang PY, Knight C, Williams M, Maxwell M, Glen RC.
    J Med Chem; 1999 Jul 15; 42(14):2504-26. PubMed ID: 10411472
    [Abstract] [Full Text] [Related]

  • 30. (Phenylpiperazinyl-butyl)oxindoles as selective 5-HT7 receptor antagonists.
    Volk B, Barkóczy J, Hegedus E, Udvari S, Gacsályi I, Mezei T, Pallagi K, Kompagne H, Lévay G, Egyed A, Hársing LG, Spedding M, Simig G.
    J Med Chem; 2008 Apr 24; 51(8):2522-32. PubMed ID: 18361484
    [Abstract] [Full Text] [Related]

  • 31. Novel 1-(azacyclyl)-3-arylsulfonyl-1H-pyrrolo[2,3-b]pyridines as 5-HT6 agonists and antagonists.
    Elokdah H, Li D, McFarlane G, Bernotas RC, Robichaud AJ, Magolda RL, Zhang GM, Smith D, Schechter LE.
    Bioorg Med Chem; 2007 Sep 15; 15(18):6208-26. PubMed ID: 17624788
    [Abstract] [Full Text] [Related]

  • 32. Designing selective, high affinity ligands of 5-HT1D receptor by covalent dimerization of 5-HT1F ligands derived from 4-fluoro-N-[3-(1-methyl-4-piperidinyl)-1H-indol-5-yl]benzamide.
    Choi SK, Green D, Ho A, Klein U, Marquess D, Taylor R, Turner SD.
    J Med Chem; 2008 Jun 26; 51(12):3609-16. PubMed ID: 18507369
    [Abstract] [Full Text] [Related]

  • 33. Extended N-Arylsulfonylindoles as 5-HT₆ Receptor Antagonists: Design, Synthesis & Biological Evaluation.
    Vera G, Lagos CF, Almendras S, Hebel D, Flores F, Valle-Corvalán G, Pessoa-Mahana CD, Mella-Raipán J, Montecinos R, Recabarren-Gajardo G.
    Molecules; 2016 Aug 16; 21(8):. PubMed ID: 27537868
    [Abstract] [Full Text] [Related]

  • 34. Synthesis and the 5-HT6 receptor antagonistic effect of 3-arylsulfonylamino-5,6-dihydro-6-substituted pyrazolo[3,4]pyridinones for neuropathic pain treatment.
    Devegowda VN, Hong JR, Cho S, Lim EJ, Choo H, Keum G, Rhim H, Nam G.
    Bioorg Med Chem Lett; 2013 Aug 15; 23(16):4696-700. PubMed ID: 23820387
    [Abstract] [Full Text] [Related]

  • 35. Design, synthesis and antifungal activity of isosteric analogues of benzoheterocyclic N-myristoyltransferase inhibitors.
    Sheng C, Xu H, Wang W, Cao Y, Dong G, Wang S, Che X, Ji H, Miao Z, Yao J, Zhang W.
    Eur J Med Chem; 2010 Sep 15; 45(9):3531-40. PubMed ID: 20615585
    [Abstract] [Full Text] [Related]

  • 36.
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    [No Abstract] [Full Text] [Related]

  • 37. Stereoselective synthesis of bioactive isosteviol derivatives as alpha-glucosidase inhibitors.
    Wu Y, Yang JH, Dai GF, Liu CJ, Tian GQ, Ma WY, Tao JC.
    Bioorg Med Chem; 2009 Feb 15; 17(4):1464-73. PubMed ID: 19167896
    [Abstract] [Full Text] [Related]

  • 38. Synthesis of 3-(2-N,N-diethylaminoethoxy)indoles as potential 5-HT6 receptor ligands.
    Alex K, Schwarz N, Khedkar V, Sayyed IA, Tillack A, Michalik D, Holenz J, Díaz JL, Beller M.
    Org Biomol Chem; 2008 May 21; 6(10):1802-7. PubMed ID: 18452016
    [Abstract] [Full Text] [Related]

  • 39. N-Arylsulfonylindole derivatives as serotonin 5-HT(6) receptor ligands.
    Russell MG, Baker RJ, Barden L, Beer MS, Bristow L, Broughton HB, Knowles M, McAllister G, Patel S, Castro JL.
    J Med Chem; 2001 Nov 08; 44(23):3881-95. PubMed ID: 11689074
    [Abstract] [Full Text] [Related]

  • 40. Synthesis and structure-affinity relationships of novel N-(1-ethyl-4-methylhexahydro-1,4-diazepin-6-yl)pyridine-3-carboxamides with potent serotonin 5-HT3 and dopamine D2 receptor antagonistic activity.
    Hirokawa Y, Fujiwara I, Suzuki K, Harada H, Yoshikawa T, Yoshida N, Kato S.
    J Med Chem; 2003 Feb 27; 46(5):702-15. PubMed ID: 12593651
    [Abstract] [Full Text] [Related]


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