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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
Availability: No items available.
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6.
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Synthesis, biological activity, and molecular modeling of selective 5-HT(2C/2B) receptor antagonists. [electronic resource] by
- Forbes, I T
- Dabbs, S
- Duckworth, D M
- Ham, P
- Jones, G E
- King, F D
- Saunders, D V
- Blaney, F E
- Naylor, C B
- Baxter, G S
- Blackburn, T P
- Kennett, G A
- Wood, M D
Producer: 19970123
In:
Journal of medicinal chemistry vol. 39
Availability: No items available.
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7.
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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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8.
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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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9.
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1-[2-[(Heteroaryloxy)heteroaryl]carbamoyl]indolines: novel and selective 5-HT2C receptor inverse agonists with potential as antidepressant/anxiolytic agents. [electronic resource] by
- Bromidge, S M
- Dabbs, S
- Davies, S
- Duckworth, D M
- Forbes, I T
- Jones, G E
- Jones, J
- King, F D
- Saunders, D V
- 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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10.
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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-HT(2C/2B) receptor antagonists. [electronic resource] by
- Bromidge, S M
- Dabbs, S
- Davies, D T
- Davies, S
- Duckworth, D M
- Forbes, I T
- Gadre, A
- Ham, P
- Jones, G E
- King, F D
- Saunders, D V
- Thewlis, K M
- Vyas, D
- Blackburn, T P
- Holland, V
- Kennett, G A
- Riley, G J
- Wood, M D
Producer: 20000323
In:
Bioorganic & medicinal chemistry vol. 7
Availability: No items available.
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11.
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The selective 5-HT1B receptor inverse agonist 1'-methyl-5-[[2'-methyl-4'-(5-methyl-1,2, 4-oxadiazol-3-yl)biphenyl-4-yl]carbonyl]-2,3,6,7-tetrahydro- spiro[furo[2,3-f]indole-3,4'-piperidine] (SB-224289) potently blocks terminal 5-HT autoreceptor function both in vitro and in vivo. [electronic resource] by
- Gaster, L M
- Blaney, F E
- Davies, S
- Duckworth, D M
- Ham, P
- Jenkins, S
- Jennings, A J
- Joiner, G F
- King, F D
- Mulholland, K R
- Wyman, P A
- Hagan, J J
- Hatcher, J
- Jones, B J
- Middlemiss, D N
- Price, G W
- Riley, G
- Roberts, C
- Routledge, C
- Selkirk, J
- Slade, P D
Producer: 19980501
In:
Journal of medicinal chemistry vol. 41
Availability: No items available.
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12.
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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. [electronic resource] by
- Bromidge, S M
- Dabbs, S
- Davies, D T
- Duckworth, D M
- Forbes, I T
- Ham, P
- Jones, G E
- King, F D
- Saunders, D V
- Starr, S
- Thewlis, K M
- Wyman, P A
- Blaney, F E
- Naylor, C B
- Bailey, F
- Blackburn, T P
- Holland, V
- Kennett, G A
- Riley, G J
- Wood, M D
Producer: 19980528
In:
Journal of medicinal chemistry vol. 41
Availability: No items available.
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13.
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Biarylcarbamoylindolines are novel and selective 5-HT(2C) 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. [electronic resource] by
- Bromidge, S M
- Dabbs, S
- Davies, D T
- Davies, S
- Duckworth, D M
- Forbes, I T
- Gaster, L M
- Ham, P
- Jones, G E
- King, F D
- Mulholland, K R
- Saunders, D V
- Wyman, P A
- Blaney, F E
- Clarke, S E
- Blackburn, T P
- Holland, V
- Kennett, G A
- Lightowler, S
- Middlemiss, D N
- Trail, B
- Riley, G J
- Wood, M D
Producer: 20000413
In:
Journal of medicinal chemistry vol. 43
Availability: No items available.
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