These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

129 related articles for article (PubMed ID: 17579384)

  • 61. Identification, synthesis, and biological evaluation of novel pyrazoles as low molecular weight luteinizing hormone receptor agonists.
    Jorand-Lebrun C; Brondyk B; Lin J; Magar S; Murray R; Reddy A; Shroff H; Wands G; Weiser W; Xu Q; McKenna S; Brugger N
    Bioorg Med Chem Lett; 2007 Apr; 17(7):2080-5. PubMed ID: 17321742
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Structural studies of Drosophila short neuropeptide F: Occurrence and receptor binding activity.
    Garczynski SF; Brown MR; Crim JW
    Peptides; 2006 Mar; 27(3):575-82. PubMed ID: 16330127
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Structure-activity relationships of neuropeptide FF and related peptidic and non-peptidic derivatives.
    Vyas N; Mollereau C; Chevé G; McCurdy CR
    Peptides; 2006 May; 27(5):990-6. PubMed ID: 16490282
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Preparation of human Melanocortin-4 receptor agonist libraries: linear peptides X-Y-DPhe7-Arg8-Trp(or 2-Nal)9-Z-NH2.
    Cheung AW; Qi L; Gore V; Chu XJ; Bartkovitz D; Kurylko G; Swistok J; Danho W; Chen L; Yagaloff K
    Bioorg Med Chem Lett; 2005 Dec; 15(24):5504-8. PubMed ID: 16203134
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Molecular basis of agonist docking in a human GPR103 homology model by site-directed mutagenesis and structure-activity relationship studies.
    Neveu C; Dulin F; Lefranc B; Galas L; Calbrix C; Bureau R; Rault S; Chuquet J; Boutin JA; Guilhaudis L; Ségalas-Milazzo I; Vaudry D; Vaudry H; Santos JS; Leprince J
    Br J Pharmacol; 2014 Oct; 171(19):4425-39. PubMed ID: 24913445
    [TBL] [Abstract][Full Text] [Related]  

  • 66. New acylated bradykinin analogues: effect on rat blood pressure and rat uterus.
    Dawidowska O; Prahl A; Wierzba T; Nowakowski L; Kowalczyk W; Slaninová J; Lammek B
    J Pept Sci; 2005 Jul; 11(7):436-9. PubMed ID: 15742339
    [TBL] [Abstract][Full Text] [Related]  

  • 67. 'Click' D(1) receptor agonists with a 5-HT(1A) receptor pharmacophore producing D(2) receptor activity.
    Zhang J; Zhang H; Cai W; Yu L; Zhen X; Zhang A
    Bioorg Med Chem; 2009 Jul; 17(14):4873-80. PubMed ID: 19559623
    [TBL] [Abstract][Full Text] [Related]  

  • 68. N(G)-acylated aminothiazolylpropylguanidines as potent and selective histamine H(2) receptor agonists.
    Kraus A; Ghorai P; Birnkammer T; Schnell D; Elz S; Seifert R; Dove S; Bernhardt G; Buschauer A
    ChemMedChem; 2009 Feb; 4(2):232-40. PubMed ID: 19072936
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Molecular cloning of the bullfrog kisspeptin receptor GPR54 with high sensitivity to Xenopus kisspeptin.
    Moon JS; Lee YR; Oh DY; Hwang JI; Lee JY; Kim JI; Vaudry H; Kwon HB; Seong JY
    Peptides; 2009 Jan; 30(1):171-9. PubMed ID: 18550222
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Synthesis and biological activity of human neuropeptide S analogues modified in position 2.
    Camarda V; Trapella C; Calo G; Guerrini R; Rizzi A; Ruzza C; Fiorini S; Marzola E; Reinscheid RK; Regoli D; Salvadori S
    J Med Chem; 2008 Feb; 51(3):655-8. PubMed ID: 18181564
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Quantitative structure activity relationship and pharmacophore studies of adenosine receptor A2B inhibitors.
    Joseph TB; Suneel Kumar BV; Santhosh B; Kriti S; Pramod AB; Ravikumar M; Kishore M
    Chem Biol Drug Des; 2008 Nov; 72(5):395-408. PubMed ID: 19012575
    [TBL] [Abstract][Full Text] [Related]  

  • 72. SAR studies of 3-arylpropionic acids as potent and selective agonists of sphingosine-1-phosphate receptor-1 (S1P1) with enhanced pharmacokinetic properties.
    Yan L; Huo P; Hale JJ; Mills SG; Hajdu R; Keohane CA; Rosenbach MJ; Milligan JA; Shei GJ; Chrebet G; Bergstrom J; Card D; Mandala SM
    Bioorg Med Chem Lett; 2007 Feb; 17(3):828-31. PubMed ID: 17092714
    [TBL] [Abstract][Full Text] [Related]  

  • 73. 3D-QSAR Based Pharmacophore Modeling and Virtual Screening for Identification of Novel G Protein-Coupled Receptor40 Agonists.
    Lu P; Wang Y; Ouyang P; She J; He M
    Curr Comput Aided Drug Des; 2015; 11(1):51-6. PubMed ID: 26022066
    [TBL] [Abstract][Full Text] [Related]  

  • 74. A high-throughput small-molecule ligand screen targeted to agonists and antagonists of the G-protein-coupled receptor GPR54.
    Kuohung W; Burnett M; Mukhtyar D; Schuman E; Ni J; Crowley WF; Glicksman MA; Kaiser UB
    J Biomol Screen; 2010 Jun; 15(5):508-17. PubMed ID: 20460252
    [TBL] [Abstract][Full Text] [Related]  

  • 75. 2,5-Disubstituted pyridines as potent GPR119 agonists.
    Wu Y; Kuntz JD; Carpenter AJ; Fang J; Sauls HR; Gomez DJ; Ammala C; Xu Y; Hart S; Tadepalli S
    Bioorg Med Chem Lett; 2010 Apr; 20(8):2577-81. PubMed ID: 20227877
    [TBL] [Abstract][Full Text] [Related]  

  • 76. FMRFamide-like peptides encoded on the flp-18 precursor gene activate two isoforms of the orphan Caenorhabditis elegans G-protein-coupled receptor Y58G8A.4 heterologously expressed in mammalian cells.
    Kubiak TM; Larsen MJ; Bowman JW; Geary TG; Lowery DE
    Biopolymers; 2008; 90(3):339-48. PubMed ID: 17879267
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Discovery and SAR of small molecule PAR1 antagonists.
    Rilatt I; Mirabel E; Le Grand B; Perez M
    Bioorg Med Chem Lett; 2010 Feb; 20(3):903-6. PubMed ID: 20042334
    [TBL] [Abstract][Full Text] [Related]  

  • 78. QSAR study for a novel series of ortho disubstituted phenoxy analogues of alpha1-adrenoceptor antagonist WB4101.
    Pallavicini M; Fumagalli L; Gobbi M; Bolchi C; Colleoni S; Moroni B; Pedretti A; Rusconi C; Vistoli G; Valoti E
    Eur J Med Chem; 2006 Sep; 41(9):1025-40. PubMed ID: 16737760
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Discovery of highly potent and selective biphenylacylsulfonamide-based beta3-adrenergic receptor agonists and evaluation of physical properties as potential overactive bladder therapies: part 5.
    Hattori K; Toda S; Imanishi M; Itou S; Nakajima Y; Washizuka K; Araki T; Hamashima H; Tomishima Y; Sakurai M; Matsui S; Imamura E; Ueshima K; Yamamoto T; Yamamoto N; Ishikawa H; Nakano K; Unami N; Hamada K; Matsumura Y; Takamura F
    J Med Chem; 2009 May; 52(9):3063-72. PubMed ID: 19366244
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Identification of selective and non-selective, biostable beta-amino acid agonists of recombinant insect kinin receptors from the southern cattle tick Boophilus microplus and mosquito Aedes aegypti.
    Taneja-Bageshwar S; Strey A; Zubrzak P; Williams H; Reyes-Rangel G; Juaristi E; Pietrantonio P; Nachman RJ
    Peptides; 2008 Feb; 29(2):302-9. PubMed ID: 18207610
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.