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Journal of Medicinal Chemistry
|
April 21, 2001
New selective cytotoxic diterpenylquinones and diterpenylhydroquinones
J M Miguel Del Corral, M Gordaliza, M A Castro, et al.
Biochemistry
|
August 16, 1994
Structural analysis of inositol monophosphatase complexes with substrates
R Bone, L Frank, J P Springer, et al.
Journal of Medicinal Chemistry
|
August 1, 1997
5-(Piperidin-2-yl)- and 5-(homopiperidin-2-yl)-1,4-benzodiazepines: high-affinity, basic ligands for the cholecystokinin-B receptor
J L Castro, H B Broughton, M G Russell, et al.
Journal of Medicinal Chemistry
|
July 18, 1997
4-Heterocyclylpiperidines as selective high-affinity ligands at the human dopamine D4 receptor
M Rowley, I Collins, H B Broughton, 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
|
May 10, 1996
3-((4-(4-Chlorophenyl)piperazin-1-yl)-methyl)-1H-pyrrolo-2,3-b-pyridine: an antagonist with high affinity and selectivity for the human dopamine D4 receptor
J J Kulagowski, H B Broughton, N R Curtis, et al.
Journal of Medicinal Chemistry
|
September 23, 2000
Development of peptide 3D structure mimetics: rational design of novel peptoid cholecystokinin receptor antagonists
C M Low, J W Black, H B Broughton, et al.
Journal of Medicinal Chemistry
|
February 16, 1996
Controlled modification of acidity in cholecystokinin B receptor antagonists: N-(1,4-benzodiazepin-3-yl)-N'-[3-(tetrazol-5-ylamino) phenyl]ureas
J L Castro, R G Ball, H B Broughton, et al.
Journal of Medicinal Chemistry
|
June 23, 1999
Fluorination of 3-(3-(piperidin-1-yl)propyl)indoles and 3-(3-(piperazin-1-yl)propyl)indoles gives selective human 5-HT1D receptor ligands with improved pharmacokinetic profiles
M B van Niel, I Collins, M S Beer, et al.
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of 2
Search research articles
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Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 19 results.
Journal of Medicinal Chemistry
|
April 21, 2001
New selective cytotoxic diterpenylquinones and diterpenylhydroquinones
J M Miguel Del Corral, M Gordaliza, M A Castro, et al.
Biochemistry
|
August 16, 1994
Structural analysis of inositol monophosphatase complexes with substrates
R Bone, L Frank, J P Springer, et al.
Journal of Medicinal Chemistry
|
August 1, 1997
5-(Piperidin-2-yl)- and 5-(homopiperidin-2-yl)-1,4-benzodiazepines: high-affinity, basic ligands for the cholecystokinin-B receptor
J L Castro, H B Broughton, M G Russell, et al.
Journal of Medicinal Chemistry
|
July 18, 1997
4-Heterocyclylpiperidines as selective high-affinity ligands at the human dopamine D4 receptor
M Rowley, I Collins, H B Broughton, 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
|
May 10, 1996
3-((4-(4-Chlorophenyl)piperazin-1-yl)-methyl)-1H-pyrrolo-2,3-b-pyridine: an antagonist with high affinity and selectivity for the human dopamine D4 receptor
J J Kulagowski, H B Broughton, N R Curtis, et al.
Journal of Medicinal Chemistry
|
September 23, 2000
Development of peptide 3D structure mimetics: rational design of novel peptoid cholecystokinin receptor antagonists
C M Low, J W Black, H B Broughton, et al.
Journal of Medicinal Chemistry
|
February 16, 1996
Controlled modification of acidity in cholecystokinin B receptor antagonists: N-(1,4-benzodiazepin-3-yl)-N'-[3-(tetrazol-5-ylamino) phenyl]ureas
J L Castro, R G Ball, H B Broughton, et al.
Journal of Medicinal Chemistry
|
June 23, 1999
Fluorination of 3-(3-(piperidin-1-yl)propyl)indoles and 3-(3-(piperazin-1-yl)propyl)indoles gives selective human 5-HT1D receptor ligands with improved pharmacokinetic profiles
M B van Niel, I Collins, M S Beer, et al.
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of 2