Results
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101.
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Functional effects of the muscarinic receptor agonist, xanomeline, at 5-HT1 and 5-HT2 receptors. [electronic resource] by
- Watson, J
- Brough, S
- Coldwell, M C
- Gager, T
- Ho, M
- Hunter, A J
- Jerman, J
- Middlemiss, D N
- Riley, G J
- Brown, A M
Producer: 19990401
In:
British journal of pharmacology vol. 125
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102.
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103.
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SB-224289--a novel selective (human) 5-HT1B receptor antagonist with negative intrinsic activity. [electronic resource] by
- Selkirk, J V
- Scott, C
- Ho, M
- Burton, M J
- Watson, J
- Gaster, L M
- Collin, L
- Jones, B J
- Middlemiss, D N
- Price, G W
Producer: 19981218
In:
British journal of pharmacology vol. 125
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104.
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SB-216641 and BRL-15572--compounds to pharmacologically discriminate h5-HT1B and h5-HT1D receptors. [electronic resource] by
- Price, G W
- Burton, M J
- Collin, L J
- Duckworth, M
- Gaster, L
- Göthert, M
- Jones, B J
- Roberts, C
- Watson, J M
- Middlemiss, D N
Producer: 19971027
In:
Naunyn-Schmiedeberg's archives of pharmacology vol. 356
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105.
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Characterization of recombinant human orexin receptor pharmacology in a Chinese hamster ovary cell-line using FLIPR. [electronic resource] by
- Smart, D
- Jerman, J C
- Brough, S J
- Rushton, S L
- Murdock, P R
- Jewitt, F
- Elshourbagy, N A
- Ellis, C E
- Middlemiss, D N
- Brown, F
Producer: 19991122
In:
British journal of pharmacology vol. 128
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106.
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Functional characterisation of the human cloned 5-HT7 receptor (long form); antagonist profile of SB-258719. [electronic resource] by
- Thomas, D R
- Gittins, S A
- Collin, L L
- Middlemiss, D N
- Riley, G
- Hagan, J
- Gloger, I
- Ellis, C E
- Forbes, I T
- Brown, A M
Producer: 19981026
In:
British journal of pharmacology vol. 124
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107.
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Cloning and characterization of human NTT5 and v7-3: two orphan transporters of the Na+/Cl- -dependent neurotransmitter transporter gene family. [electronic resource] by
- Farmer, M K
- Robbins, M J
- Medhurst, A D
- Campbell, D A
- Ellington, K
- Duckworth, M
- Brown, A M
- Middlemiss, D N
- Price, G W
- Pangalos, M N
Producer: 20010208
In:
Genomics vol. 70
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108.
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Synthesis and serotonergic activity of 5-(oxadiazolyl)tryptamines: potent agonists for 5-HT1D receptors. [electronic resource] by
- Street, L J
- Baker, R
- Castro, J L
- Chambers, M S
- Guiblin, A R
- Hobbs, S C
- Matassa, V G
- Reeve, A J
- Beer, M S
- Middlemiss, D N
Producer: 19930621
In:
Journal of medicinal chemistry vol. 36
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109.
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Structure and activity of hydrogenated derivatives of (+)-5-methyl-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5,10-imine (MK-801). [electronic resource] by
- Lyle, T A
- Magill, C A
- Britcher, S F
- Denny, G H
- Thompson, W J
- Murphy, J S
- Knight, A R
- Kemp, J A
- Marshall, G R
- Middlemiss, D N
Producer: 19900406
In:
Journal of medicinal chemistry vol. 33
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110.
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Characterization of SB-271046: a potent, selective and orally active 5-HT(6) receptor antagonist. [electronic resource] by
- Routledge, C
- Bromidge, S M
- Moss, S F
- Price, G W
- Hirst, W
- Newman, H
- Riley, G
- Gager, T
- Stean, T
- Upton, N
- Clarke, S E
- Brown, A M
- Middlemiss, D N
Producer: 20010125
In:
British journal of pharmacology vol. 130
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111.
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The selective 5-HT1B receptor inverse agonist SB-224289, potently blocks terminal 5-HT autoreceptor function both in vitro and in vivo. [electronic resource] by
- Gaster, L M
- Ham, P
- Joiner, G F
- King, F D
- Mulholland, K R
- Wyman, P A
- Hagan, J J
- Price, G W
- Roberts, C
- Routledge, C
- Selkirk, J
- Slade, P D
- Middlemiss, D N
Producer: 19990225
In:
Annals of the New York Academy of Sciences vol. 861
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112.
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SB 242084, a selective and brain penetrant 5-HT2C receptor antagonist. [electronic resource] by
- Kennett, G A
- Wood, M D
- Bright, F
- Trail, B
- Riley, G
- Holland, V
- Avenell, K Y
- Stean, T
- Upton, N
- Bromidge, S
- Forbes, I T
- Brown, A M
- Middlemiss, D N
- Blackburn, T P
Producer: 19970915
In:
Neuropharmacology vol. 36
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113.
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(R)-3,N-dimethyl-N-[1-methyl-3-(4-methyl-piperidin-1-yl) propyl]benzenesulfonamide: the first selective 5-HT7 receptor antagonist. [electronic resource] by
- Forbes, I T
- Dabbs, S
- Duckworth, D M
- Jennings, A J
- King, F D
- Lovell, P J
- Brown, A M
- Collin, L
- Hagan, J J
- Middlemiss, D N
- Riley, G J
- Thomas, D R
- Upton, N
Producer: 19980414
In:
Journal of medicinal chemistry vol. 41
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114.
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The expression of GABA(B1) and GABA(B2) receptor subunits in the cNS differs from that in peripheral tissues. [electronic resource] by
- Calver, A R
- Medhurst, A D
- Robbins, M J
- Charles, K J
- Evans, M L
- Harrison, D C
- Stammers, M
- Hughes, S A
- Hervieu, G
- Couve, A
- Moss, S J
- Middlemiss, D N
- Pangalos, M N
Producer: 20001106
In:
Neuroscience vol. 100
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115.
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SB-243213; a selective 5-HT2C receptor inverse agonist with improved anxiolytic profile: lack of tolerance and withdrawal anxiety. [electronic resource] by
- Wood, M D
- Reavill, C
- Trail, B
- Wilson, A
- Stean, T
- Kennett, G A
- Lightowler, S
- Blackburn, T P
- Thomas, D
- Gager, T L
- Riley, G
- Holland, V
- Bromidge, S M
- Forbes, I T
- Middlemiss, D N
Producer: 20011011
In:
Neuropharmacology vol. 41
Availability: No items available.
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116.
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Characterization of SB-269970-A, a selective 5-HT(7) receptor antagonist. [electronic resource] by
- Hagan, J J
- Price, G W
- Jeffrey, P
- Deeks, N J
- Stean, T
- Piper, D
- Smith, M I
- Upton, N
- Medhurst, A D
- Middlemiss, D N
- Riley, G J
- Lovell, P J
- Bromidge, S M
- Thomas, D R
Producer: 20000801
In:
British journal of pharmacology vol. 130
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117.
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SB-272183, a selective 5-HT(1A), 5-HT(1B) and 5-HT(1D) receptor antagonist in native tissue. [electronic resource] by
- Watson, J
- Roberts, C
- Scott, C
- Kendall, I
- Collin, L
- Day, N C
- Harries, M H
- Soffin, E
- Davies, C H
- Randall, A D
- Heightman, T
- Gaster, L
- Wyman, P
- Parker, C
- Price, G W
- Middlemiss, D N
Producer: 20010906
In:
British journal of pharmacology vol. 133
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118.
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5-Chloro-N-(4-methoxy-3-piperazin-1-yl- phenyl)-3-methyl-2-benzothiophenesulfon- amide (SB-271046): a potent, selective, and orally bioavailable 5-HT6 receptor antagonist. [electronic resource] by
- Bromidge, S M
- Brown, A M
- Clarke, S E
- Dodgson, K
- Gager, T
- Grassam, H L
- Jeffrey, P M
- Joiner, G F
- King, F D
- Middlemiss, D N
- Moss, S F
- Newman, H
- Riley, G
- Routledge, C
- Wyman, P
Producer: 19990304
In:
Journal of medicinal chemistry vol. 42
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119.
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A novel, potent, and selective 5-HT(7) antagonist: (R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolidine-1-sulfonyl) phen ol (SB-269970). [electronic resource] by
- Lovell, P J
- Bromidge, S M
- Dabbs, S
- Duckworth, D M
- Forbes, I T
- Jennings, A J
- King, F D
- Middlemiss, D N
- Rahman, S K
- Saunders, D V
- Collin, L L
- Hagan, J J
- Riley, G J
- Thomas, D R
Producer: 20000313
In:
Journal of medicinal chemistry vol. 43
Availability: No items available.
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120.
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1-[2-[(Heteroarylmethoxy)aryl]carbamoyl]indolines are selective and orally active 5-HT2C receptor inverse agonists. [electronic resource] by
- Bromidge, S M
- Davies, S
- Duckworth, D M
- Forbes, I T
- Jones, G E
- Jones, J
- King, F D
- Blackburn, T P
- Holland, V
- Kennett, G A
- Lightowler, S
- Middlemiss, D N
- Riley, G J
- Trail, B
- Wood, M D
Producer: 20010118
In:
Bioorganic & medicinal chemistry letters vol. 10
Availability: No items available.
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