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Bioorganic & Medicinal Chemistry Letters
|
September 25, 1999
2,7-diazabicyclo[3.3.0]octanes as novel h5-HT receptor agonists
M G Russell, M S Beer, J A Stanton, et al.
Journal of Medicinal Chemistry
|
July 21, 1998
Enhancement of oral absorption in selective 5-HT1D receptor agonists: fluorinated 3-[3-(piperidin-1-yl)propyl]indoles
J L Castro, I Collins, M G Russell, et al.
British Journal of Pharmacology
|
November 1, 1993
L-694,247: a potent 5-HT1D receptor agonist
M S Beer, J A Stanton, Y Bevan, et al.
Journal of Medicinal Chemistry
|
November 14, 1997
3-[2-(Pyrrolidin-1-yl)ethyl]indoles and 3-[3-(piperidin-1-yl)propyl]indoles: agonists for the h5-HT1D receptor with high selectivity over the h5-HT1B subtype
J L Castro, L J Street, A R Guiblin, et al.
Journal of Medicinal Chemistry
|
November 14, 1997
Selective, orally active 5-HT1D receptor agonists as potential antimigraine agents
A M MacLeod, L J Street, A J Reeve, et al.
Journal of Medicinal Chemistry
|
September 16, 1994
Synthesis and biological activity of 3-[2-(dimethylamino)ethyl]-5-[(1,1-dioxo-5-methyl-1,2,5-thiadiazolidin- 2-yl)-methyl]-1H-indole and analogues: agonists for the 5-HT1D receptor
J L Castro, R Baker, A R Guiblin, et al.
Neuropharmacology
|
May 24, 2003
The hypothermic effect of 5-CT in mice is mediated through the 5-HT7 receptor
M R Guscott, E Egan, G P Cook, et al.
Journal of Medicinal Chemistry
|
December 10, 1999
3-[3-(Piperidin-1-yl)propyl]indoles as highly selective h5-HT(1D) receptor agonists
M G Russell, V G Matassa, R R Pengilley, et al.
Journal of Medicinal Chemistry
|
March 3, 1999
Synthesis and serotonergic activity of 3-[2-(pyrrolidin-1-yl)ethyl]indoles: potent agonists for the h5-HT1D receptor with high selectivity over the h5-HT1B receptor
F Sternfeld, A R Guiblin, R A Jelley, et al.
Journal of Medicinal Chemistry
|
March 3, 1999
3-(Piperazinylpropyl)indoles: selective, orally bioavailable h5-HT1D receptor agonists as potential antimigraine agents
M S Chambers, L J Street, S Goodacre, et al.
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Search research articles
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Showing results (21-30 of 32) with videos related to
Sort By:
Page
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Bioorganic & Medicinal Chemistry Letters
|
September 25, 1999
2,7-diazabicyclo[3.3.0]octanes as novel h5-HT receptor agonists
M G Russell, M S Beer, J A Stanton, et al.
Journal of Medicinal Chemistry
|
July 21, 1998
Enhancement of oral absorption in selective 5-HT1D receptor agonists: fluorinated 3-[3-(piperidin-1-yl)propyl]indoles
J L Castro, I Collins, M G Russell, et al.
British Journal of Pharmacology
|
November 1, 1993
L-694,247: a potent 5-HT1D receptor agonist
M S Beer, J A Stanton, Y Bevan, et al.
Journal of Medicinal Chemistry
|
November 14, 1997
3-[2-(Pyrrolidin-1-yl)ethyl]indoles and 3-[3-(piperidin-1-yl)propyl]indoles: agonists for the h5-HT1D receptor with high selectivity over the h5-HT1B subtype
J L Castro, L J Street, A R Guiblin, et al.
Journal of Medicinal Chemistry
|
November 14, 1997
Selective, orally active 5-HT1D receptor agonists as potential antimigraine agents
A M MacLeod, L J Street, A J Reeve, et al.
Journal of Medicinal Chemistry
|
September 16, 1994
Synthesis and biological activity of 3-[2-(dimethylamino)ethyl]-5-[(1,1-dioxo-5-methyl-1,2,5-thiadiazolidin- 2-yl)-methyl]-1H-indole and analogues: agonists for the 5-HT1D receptor
J L Castro, R Baker, A R Guiblin, et al.
Neuropharmacology
|
May 24, 2003
The hypothermic effect of 5-CT in mice is mediated through the 5-HT7 receptor
M R Guscott, E Egan, G P Cook, et al.
Journal of Medicinal Chemistry
|
December 10, 1999
3-[3-(Piperidin-1-yl)propyl]indoles as highly selective h5-HT(1D) receptor agonists
M G Russell, V G Matassa, R R Pengilley, et al.
Journal of Medicinal Chemistry
|
March 3, 1999
Synthesis and serotonergic activity of 3-[2-(pyrrolidin-1-yl)ethyl]indoles: potent agonists for the h5-HT1D receptor with high selectivity over the h5-HT1B receptor
F Sternfeld, A R Guiblin, R A Jelley, et al.
Journal of Medicinal Chemistry
|
March 3, 1999
3-(Piperazinylpropyl)indoles: selective, orally bioavailable h5-HT1D receptor agonists as potential antimigraine agents
M S Chambers, L J Street, S Goodacre, et al.
Page
of 4