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La ricerca find articoli where authors phrase all words 'Bromidge, SM' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 20 riferimenti
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    1. Bromidge, SM; Griffith, K; Heightman, TD; Jennings, A; King, FD; Moss, SF; Newman, H; Riley, G; Routledge, C; Serafinowska, HT; Thomas, DR
      Novel (4-piperazin-1-ylquinolin-6-yl) arylsulfonamides with high affinity and selectivity for the 5-HT6 receptor

      BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
    2. Bromidge, SM; Clarke, SE; Gager, T; Griffith, K; Jeffrey, P; Jennings, AJ; Joiner, GF; King, FD; Lovell, PJ; Moss, SF; Newman, H; Riley, G; Rogers, D; Routledge, C; Serafinowska, H; Smith, DR
      Phenyl benzenesulfonamides are novel and selective 5-HT6 antagonists: Identification of N-(2,5-dibromo-3-fluorophenyl)-4-methoxy-3-piperazin-1-ylbenzenesulfonamide (SB-357134)

      BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
    3. Wood, MD; Reavill, C; Trail, B; Wilson, A; Stean, T; Kennett, GA; Lightowler, S; Blackburn, TP; Thomas, D; Gager, TL; Riley, G; Holland, V; Bromidge, SM; Forbes, IT; Middlemiss, DN
      SB-243213; a selective 5-HT2C receptor inverse agonist with improved anxiolytic profile: lack of tolerance and withdrawal anxiety

      NEUROPHARMACOLOGY
    4. Bromidge, SM; Dabbs, S; Davies, S; Duckworth, DM; Forbes, IT; Jones, GE; Jones, J; King, FD; Saunders, DV; Blackburn, TP; Holland, V; Kennett, GA; Lightowler, S; Middlemiss, DN; Riley, GJ; Trail, B; Wood, MD
      1-[2-[(heteroaryloxy)heteroaryl]carbamoyl]indolines: Novel and selective 5-HT2C receptor inverse agonists with potential as antidepressant/anxiolyticagents

      BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
    5. Bromidge, SM; Davies, S; Duckworth, DM; Forbes, IT; Jones, GE; Jones, J; King, FD; Blackburn, TP; Holland, V; Kennett, GA; Lightowler, S; Middlemiss, DN; Riley, GJ; Trail, B; Wood, MD
      1-[2-[(heteroarylmethoxy)aryl]carbamoyl]indolines are selective and orallyactive 5-HT2C receptor inverse agonists

      BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
    6. Bromidge, SM; Dabbs, S; Davies, DT; Davies, S; Duckworth, DM; Forbes, IT; Gaster, LM; Ham, P; Jones, GE; King, FD; Mulholland, KR; Saunders, DV; Wyman, PA; Blaney, FE; Clarke, SE; Blackburn, TP; Holland, V; Kennett, GA; Lightowler, S; Middlemiss, DN; Trail, B; Riley, GJ; Wood, MD
      Biarylcarbamoylindolines are novel and selective 5-HT2C receptor inverse agonists: Identification of 5-methyl-1-[[2-[(2-methyl-3-pyridyl)oxy]-5-pyridyl]carbamoyl]-6-trifluoromethylindoline (SB-243213) as a potential antidepressant/anxiolytic agent

      JOURNAL OF MEDICINAL CHEMISTRY
    7. Lovell, PJ; Bromidge, SM; Dabbs, S; Duckworth, DM; Forbes, IT; Jennings, AJ; King, FD; Middlemiss, DN; Rahman, SK; Saunders, DV; Collin, LL; Hagan, JJ; Riley, GJ; Thomas, DR
      A novel, potent, and selective 5-HT7 antagonist: (R)-3-(2-(2-(4-methylpiperidin-1-yl)-ethyl)pyrrolidine-1-sulfonyl)phenol (SB-269970)

      JOURNAL OF MEDICINAL CHEMISTRY
    8. Hirst, WD; Minton, JAL; Bromidge, SM; Moss, SF; Latter, AJ; Riley, G; Routledge, C; Middlemiss, DN; Price, GW
      Characterization of [I-125]-SB-258585 binding to human recombinant and native 5-HT6 receptors in rat, pig and human brain tissue

      BRITISH JOURNAL OF PHARMACOLOGY
    9. Routledge, C; Bromidge, SM; Moss, SF; Price, GW; Hirst, W; Newman, H; Riley, G; Gager, T; Stean, T; Upton, N; Clarke, SE; Brown, AM; Middlemiss, DN
      Characterization of SB-271046: A potent, selective and orally active 5-HT6receptor antagonist

      BRITISH JOURNAL OF PHARMACOLOGY
    10. Hagan, JJ; Price, GW; Jeffrey, P; Deeks, NJ; Stean, T; Piper, D; Smith, MI; Upton, N; Medhurst, AD; Middlemiss, DN; Riley, GJ; Lovell, PJ; Bromidge, SM; Thomas, DR
      Characterization of SB-269970-A, a selective 5-HT7 receptor antagonist

      BRITISH JOURNAL OF PHARMACOLOGY
    11. Thomas, DR; Atkinson, PJ; Ho, M; Bromidge, SM; Lovell, PJ; Villani, AJ; Hagan, JJ; Middlemiss, DN; Price, GW
      [H-3]-SB-269970 - A selective antagonist radioligand for 5-HT7 receptors

      BRITISH JOURNAL OF PHARMACOLOGY
    12. Bromidge, SM; Dabbs, S; Davies, DT; Davies, S; Duckworth, DM; Forbes, IT; Gadre, A; Ham, P; Jones, GE; King, FD; Saunders, DV; Thewlis, KM; Vyas, D; Blackburn, TP; Holland, V; Kennett, GA; Riley, GJ; Wood, MD
      Model studies on a synthetically facile series of N-substituted phenyl-N '-pyridin-3-yl ureas leading to 1-(3-pyridylcarbamoyl) indolines that are potent and selective 5-HT2C/2B receptor antagonists

      BIOORGANIC & MEDICINAL CHEMISTRY
    13. Bromidge, SM; Brown, AM; Clarke, SE; Dodgson, K; Gager, T; Grassam, HL; Jeffrey, PM; Joiner, GF; King, FD; Middlemiss, DN; Moss, SF; Newman, H; Riley, G; Routledge, C; Wyman, P
      5-chloro-N-(4-methoxy-3-piperazin-1-yl-phenyl)-3-methyl-2-benzothiophenesulfonamide (SB-271046): A potent, selective, and orally bioavailable 5-HT6 receptor antagonist

      JOURNAL OF MEDICINAL CHEMISTRY
    14. BROMIDGE SM; DABBS S; DAVIES DT; DUCKWORTH DM; FORBES IT; HAM P; JONES GE; KING FD; SAUNDERS DV; STARR S; THEWLIS KM; WYMAN PA; BLANEY FE; NAYLOR CB; BAILEY F; BLACKBURN TP; HOLLAND V; KENNETT GA; RILEY GJ; WOOD MD
      NOVEL AND SELECTIVE 5-HT2C 2B RECEPTOR ANTAGONISTS AS POTENTIAL ANXIOLYTIC AGENTS - SYNTHESIS, QUANTITATIVE STRUCTURE-ACTIVITY-RELATIONSHIPS, AND MOLECULAR MODELING OF SUBSTITUTED 1-(3-PYRIDYLCARBAMOYL)INDOLINES/

      Journal of medicinal chemistry
    15. LOUDON JM; BROMIDGE SM; BROWN F; CLARK MSG; HATCHER JP; HAWKINS J; RILEY GJ; NOY G; ORLEK BS
      SE-202026 - A NOVEL MUSCARINIC PARTIAL AGONIST WITH FUNCTIONAL SELECTIVITY FOR M-1 RECEPTORS

      The Journal of pharmacology and experimental therapeutics
    16. BROMIDGE SM; BROWN F; CASSIDY F; CLARK MSG; DABBS S; HADLEY MS; HAWKINS J; LOUDON JM; NAYLOR CB; ORLEK BS; RILEY GJ
      DESIGN OF OXYIMINO)-1-AZABICYCLO[2.2.2]OCTANE-3-ACETONITRILE (SB-202026), A FUNCTIONALLY SELECTIVE AZABICYCLIC MUSCARINIC M1 AGONIST INCORPORATING THE N-METHOXY IMIDOYL NITRILE GROUP AS A NOVEL ESTER BIOISOSTERE())

      Journal of medicinal chemistry
    17. BROMIDGE SM; DUCKWORTH M; FORBES IT; HAM P; KING FD; THEWLIS KM; BLANEY FE; NAYLOR CB; BLACKBURN TP; KENNETT GA; WOOD MD; CLARKE SE
      ETHYL-3-PYRIDYL)OXY]-5-PYRIDYL]CARBAMOYL]-INDOLINE (SB-242084) - THE FIRST SELECTIVE AND BRAIN PENETRANT 5-HT2C RECEPTOR ANTAGONIST

      Journal of medicinal chemistry
    18. BROMIDGE SM; BROWN F; CASSIDY F; CLARK MSG; COLLINGS EJ; DABBS S; FAULKNER RE; LOUDON JM; ORLEK BS; RILEY GJ
      1,2,5,6-TETRAHYDROPYRIDINE OXIME ETHERS INCORPORATING ELECTRON-WITHDRAWING GROUPS ARE POTENT AND SELECTIVE MUSCARINIC AGONISTS

      Bioorganic & medicinal chemistry letters
    19. BROMIDGE SM; CASSIDY F; CLARK MSG; FAULKNER RE; HADLEY MS; ORLEK BS; RILEY GJ; STEMP G
      BRIDGED 1,2,5,6-TETRAHYDROPYRIDINE ESTERS AND OXIME ETHERS RELATED TOARECOLINE ARE NOVEL AND POTENT MUSCARINIC AGONISTS

      Bioorganic & medicinal chemistry letters
    20. BROMIDGE SM; CASSIDY F; CLARK MSG; EGGLESTON DS; ORIEK BS
      SYNTHESIS AND PROPERTIES OF (1-AZABICYCLO[2.2.2]OCT-3-YL)-ALPHA-(METHOXYIMINO) ACETONITRILE, A NOVEL FUNCTIONALLY SELECTIVE MUSCARINIC PARTIAL AGONIST())

      Journal of the Chemical Society, Chemical Communications


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 11/08/20 alle ore 19:20:21