Search Results - "BOURRAIN, Sylvie"

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    Synthesis of pyrido[2,3- d]pyridazines and pyrazino[2,3- d]-pyridazines—novel classes of GABA A receptor benzodiazepine binding site ligands by Mitchinson, Andrew, Blackaby, Wesley P., Bourrain, Sylvie, Carling, Robert W., Lewis, Richard T.

    Published in Tetrahedron letters (27-03-2006)
    “…Novel syntheses of 2,3,8-trisubstituted pyrido[2,3- d]pyridazines and 2,3,5-trisubstituted pyrazino[2,3- d]pyridazines are described. Two complementary routes…”
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    3-(4-Piperidinyl)- and 3-(8-aza-bicyclo[3.2.1]oct-3-yl)-2-phenyl-1h-indoles as bioavailable h5-HT2A antagonists by CRAWFORTH, James, GOODACRE, Simon, MAXEY, Robert, BOURRAIN, Sylvie, PATEL, Smita, MARWOOD, Rosemarie, O'CONNOR, Desmond, HERBERT, Richard, HUTSON, Peter, ROWLEY, Michael

    Published in Bioorganic & medicinal chemistry letters (18-12-2000)
    “…A series of 3-(4-piperidinyl)- and 3-(8-aza-bicyclo[3.2.1]oct-3-yl)-2-phenyl-1H-indoles have been prepared and evaluated as ligands for the h5-HT2A receptor…”
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    3-(4-Piperidinyl)- and 3-(8-aza-bicyclo[3.2.1]oct-3-yl)-2-phenyl-1 H-indoles as bioavailable h5-HT 2A antagonists by Crawforth, James, Goodacre, Simon, Maxey, Robert, Bourrain, Sylvie, Patel, Smita, Marwood, Rosemarie, O'Connor, Desmond, Herbert, Richard, Hutson, Peter, Rowley, Michael

    “…A series of 3-(4-piperidinyl)- and 3-(8-aza-bicyclo[3.2.l]oct-3-yl)-2-phenyl-1 H-indoles have been prepared and evaluated as ligands for the h5-HT 2A receptor…”
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    Substituted pyrazoles as novel selective ligands for the human dopamine D4 receptor by Bourrain, S, Collins, I, Neduvelil, J G, Rowley, M, Leeson, P D, Patel, S, Emms, F, Marwood, R, Chapman, K L, Fletcher, A E, Showell, G A

    Published in Bioorganic & medicinal chemistry (01-10-1998)
    “…Two novel series of 3-(heterocyclylmethyl)pyrazoles have been synthesised and evaluated as ligands for the human dopamine D4 receptor. Compounds in series I…”
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    4-Hydroxy-1-[3-(5-(1,2,4-triazol-4-yl)-1 H-indol-3-yl)propyl]piperidines: Selective h5-HT 1D agonists for the treatment of migraine by Bourrain, Sylvie, Neduvelil, Joseph G., Beer, Margaret S., Stanton, Josephine A., Showell, Graham A., MacLeod, Angus M.

    “…A series of 4-hydroxy-1-[3-(5-(1,2,4-triazol-4-yl)-1 H-indol-3-yl)propyl] piperidines was investigated as potential selective h5-HT 1D agonists for the…”
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    4-Hydroxy-1-[3-(5-(1,2,4-triazol-4-yl)-1H-indol-3-yl)propyl]piperidines : Selective h5-HT1D agonists for the treatment of migraine by BOURRAIN, S, NEDUVELIL, J. G, BEER, M. S, STANTON, J. A, SHOWELL, G. A, MACLEOD, A. M

    Published in Bioorganic & medicinal chemistry letters (06-12-1999)
    “…A series of 4-hydroxy-1-[3-(5-(1,2,4-triazol-4-yl)-1H-indol-3-yl)propyl] piperidines was investigated as potential selective h5-HT1D agonists for the treatment…”
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    Biological properties of the benzodiazepine amidine derivative L-740,093, a cholecystokinin-B/gastrin receptor antagonist with high affinity in vitro and high potency in vivo by Patel, S, Smith, A J, Chapman, K L, Fletcher, A E, Kemp, J A, Marshall, G R, Hargreaves, R J, Ryecroft, W, Iversen, L L, Iversen, S D

    Published in Molecular pharmacology (01-11-1994)
    “…A novel series of 5-amino-1,4-benzodiazepin-2-one derivatives (amidines), which contain a cationic solubilizing group and which are antagonists for the…”
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