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La ricerca find articoli where authors phrase all words 'FORBES IT' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 28 riferimenti
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    1. Witherington, J; Bordas, V; Cooper, DG; Forbes, IT; Gribble, AD; Ife, RJ; Berkhout, T; Gohil, J; Groot, PHE
      Conformationally restricted indolopiperidine derivatives as potent CCR2B receptor antagonists

      BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
    2. Forbes, IT
      A short and efficient synthesis of N-substituted indol-2-ones (oxindoles)

      TETRAHEDRON 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. Forbes, IT; Cooper, DG; Dodds, EK; Hickey, DMB; Ife, RJ; Meeson, M; Stockley, M; Berkhout, TA; Gohil, J; Groot, PHE; Moores, K
      CCR2B receptor antagonists: Conversion of a weak HTS hit to a potent lead compound

      BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
    5. 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
    6. 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
    7. 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
    8. 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
    9. 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
    10. Forbes, IT
      Highly stereoselective synthesis of exo and endo indolotropanes

      TETRAHEDRON LETTERS
    11. FORBES IT; DABBS S; DUCKWORTH DM; JENNINGS AJ; KING FD; LOVELL PJ; BROWN AM; COLLIN L; HAGAN JJ; MIDDLEMISS DN; RILEY GJ; THOMAS DR; UPTON N
      (4-METHYL-PIPERIDIN-1-YL)PROPYL]BENZENESULFONAMIDE - THE FIRST SELECTIVE 5-HT7 RECEPTOR ANTAGONIST

      Journal of medicinal chemistry
    12. 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
    13. THOMAS DR; GITTINS SA; COLLIN LL; MIDDLEMISS DN; RILEY G; HAGAN J; GLOGER I; ELLIS CE; FORBES IT; BROWN AM
      FUNCTIONAL-CHARACTERIZATION OF THE HUMAN CLONED 5-HT7 RECEPTOR (LONG FORM) - ANTAGONIST PROFILE OF SB-258719

      British Journal of Pharmacology
    14. KENNETT GA; WOOD MD; BRIGHT F; TRAIL B; RILEY G; HOLLAND V; AVENELL KY; STEAN T; UPTON N; BROMIDGE S; FORBES IT; BROWN AM; MIDDLEMISS DN; BLACKBURN TP
      SB-242084, A SELECTIVE AND BRAIN PENETRANT 5-HT2C RECEPTOR ANTAGONIST

      Neuropharmacology
    15. 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
    16. DAVISON EC; FORBES IT; HOLMES AB; WARNER JA
      N-ALKENYL NITRONE DIPOLAR CYCLOADDITION ROUTES TO PIPERIDINES AND INDOLIZIDINES .8. THE SCOPE OF TANDEM REACTIONS INVOLVING HYDROXYLAMINE-ALKYNE CYCLIZATIONS

      Tetrahedron
    17. FORBES IT; MORGAN HKA; THOMPSON M
      A SYNTHESIS OF NOVEL IH-IMIDAZO[1,2-ALPHA]INDOLE-3-CARBOXYLATES

      Synthetic communications
    18. FORBES IT; DABBS S; DUCKWORTH DM; HAM P; JONES GE; KING FD; SAUNDERS DV; BLANEY FE; NAYLOR CB; BAXTER GS; BLACKBURN TP; KENNETT GA; WOOD MD
      SYNTHESIS, BIOLOGICAL-ACTIVITY, AND MOLECULAR MODELING STUDIES OF SELECTIVE 5-HT2C 2B RECEPTOR ANTAGONISTS/

      Journal of medicinal chemistry
    19. KENNETT GA; WOOD MD; BRIGHT F; CILIA J; PIPER DC; GAGER T; THOMAS D; BAXTER GS; FORBES IT; HAM P; BLACKBURN TP
      IN-VITRO AND IN-VIVO PROFILE OF SB-206553, A POTENT 5-HT2C 5-HT2B RECEPTOR ANTAGONIST WITH ANXIOLYTIC-LIKE PROPERTIES/

      British Journal of Pharmacology
    20. BLACKBURN TP; DAVIES DT; FORBES IT; HAYWARD CJ; JOHNSON CN; MARTIN RT; PIPER DC; THOMAS DR; THOMPSON M; UPTON N; WARD RW
      ISOSTERIC REPLACEMENT OF THE INDOLE NUCLEUS BY BENZOTHIOPHENE IN A SERIES OF PYRIDO[2,3-B]INDOLES WITH POTENTIAL ANXIOLYTIC ACTIVITY

      Bioorganic & medicinal chemistry letters
    21. DAVISON EC; HOLMES AB; FORBES IT
      A TANDEM SYNTHESIS OF (+ -)-EUPHOCOCCININE AND (+/-)-ADALINE/

      Tetrahedron letters
    22. FORBES IT; JONES GE; MURPHY OE; HOLLAND V; BAXTER GS
      METHYL-5-INDOLYL)-N'-(3-METHYL-5-ISOTHIAZOLYL)UREA - A NOVEL, HIGH-AFFINITY 5-HT2B RECEPTOR ANTAGONIST

      Journal of medicinal chemistry
    23. FORBES IT; HAM P; BOOTH DH; MARTIN RT; THOMPSON M; BAXTER GS; BLACKBURN TP; GLEN A; KENNETT GA; WOOD MD
      LCARBAMOYL)-1,2,3,5-TETRAHYDROPYRROLO[2,3-F]INDOLE - A NOVEL 5-HT2C 5-HT2B RECEPTOR ANTAGONIST WITH IMPROVED AFFINITY, SELECTIVITY, AND ORAL ACTIVITY

      Journal of medicinal chemistry
    24. BAXTER GS; ELLIS ES; FORBES IT; JONES GE; KENNETT GA
      SB-204741 - A POTENT AND SELECTIVE ANTAGONIST AT 5-HT(2B) RECEPTORS

      British Journal of Pharmacology
    25. BLACKBURN TP; BOLTON D; FORBES IT; JOHNSON CN; MARTIN RT; THOMAS DR; THOMPSON M; UPTON N
      -DIMETHYL-1,2,3,4-TETRAHYDRO-6H-QUININDOLIN-1-ONE, A NOVEL GABA(A) MODULATOR WITH POTENTIAL ANXIOLYTIC ACTIVITY

      Bioorganic & medicinal chemistry letters
    26. FOX ME; HOLMES AB; FORBES IT; THOMPSON M
      N-ALKENYL NITRONE DIPOLAR CYCLOADDITION ROUTES TO PIPERIDINES AND INDOLIZIDINES .7. HYDROXYLAMINE ALKYNE CYCLIZATIONS - FORMATION OF CYCLICNITRONES AND APPLICATION TO THE SYNTHESIS OF THE PROPOSED STRUCTURE FOR (+ -)-ACACIALACTAM/

      Journal of the Chemical Society. Perkin transactions. I
    27. BOLTON D; FORBES IT; HAYWARD CJ; PIPER DC; THOMAS DR; THOMPSON M; UPTON N
      SYNTHESIS AND POTENTIAL ANXIOLYTIC ACTIVITY OF 4-AMINO-PYRIDO[2,3-B]INDOLES

      Bioorganic & medicinal chemistry letters
    28. FORBES IT; KENNETT GA; GADRE A; HAM P; HAYWARD CJ; MARTIN RT; THOMPSON M; WOOD MD; BAXTER GS; GLEN A; MURPHY OE; STEWART BA; BLACKBURN TP
      N-(1-METHYL-5-INDOLYL)-N'-(3-PYRIDYL)UREA HYDROCHLORIDE - THE 1ST SELECTIVE 5-HT(1C) RECEPTOR ANTAGONIST

      Journal of medicinal chemistry


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 28/10/20 alle ore 21:51:14