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Journal of Molecular Graphics & Modelling
|
January 6, 2001
Visualizing substructural fingerprints
R D Clark, D E Patterson, F Soltanshahi, et al.
Journal of Pharmaceutical Sciences
|
April 3, 1999
Inclusion complexation of ziprasidone mesylate with beta-cyclodextrin sulfobutyl ether
Y Kim, D A Oksanen, W Massefski, et al.
Neuropharmacology
|
December 1, 1993
Antagonism of baclofen-induced depression of whole-cell synaptic currents in spinal dorsal horn neurones by the potent GABAB antagonist CGP55845
J F Blake, C Q Cao, P M Headley, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 31, 2000
Design, synthesis and biological evaluation of 3-amino-3-phenylpropionamide derivatives as novel mu opioid receptor ligands
M P Allen, J F Blake, D K Bryce, et al.
Journal of Medicinal Chemistry
|
November 22, 1996
Glucose transport-enhancing and hypoglycemic activity of 2-methyl-2-phenoxy-3-phenylpropanoic acids
R Sarges, R F Hank, J F Blake, et al.
Journal of Medicinal Chemistry
|
May 18, 2001
Quinazolin-4-one alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor antagonists: structure-activity relationship of the C-2 side chain tether
B L Chenard, W M Welch, J F Blake, et al.
Journal of Medicinal Chemistry
|
August 19, 1994
Novel benzisoxazole derivatives as potent and selective inhibitors of acetylcholinesterase
A Villalobos, J F Blake, C K Biggers, et al.
Journal of Medicinal Chemistry
|
July 6, 2000
Structure-based design and synthesis of a potent matrix metalloproteinase-13 inhibitor based on a pyrrolidinone scaffold
R P Robinson, E R Laird, J F Blake, et al.
Journal of Medicinal Chemistry
|
April 17, 1998
(3R,4S)-3-[4-(4-fluorophenyl)-4-hydroxypiperidin-1-yl]chroman-4,7-diol: a conformationally restricted analogue of the NR2B subtype-selective NMDA antagonist (1S,2S)-1-(4-hydroxyphenyl)-2-(4-hydroxy-4-phenylpiperidino)- 1-propanol
T W Butler, J F Blake, J Bordner, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 18, 1999
Inhibition of MMP-1 and MMP-13 with phosphinic acids that exploit binding in the S2 pocket
L A Reiter, J P Rizzi, J Pandit, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 20) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 20 results.
Journal of Molecular Graphics & Modelling
|
January 6, 2001
Visualizing substructural fingerprints
R D Clark, D E Patterson, F Soltanshahi, et al.
Journal of Pharmaceutical Sciences
|
April 3, 1999
Inclusion complexation of ziprasidone mesylate with beta-cyclodextrin sulfobutyl ether
Y Kim, D A Oksanen, W Massefski, et al.
Neuropharmacology
|
December 1, 1993
Antagonism of baclofen-induced depression of whole-cell synaptic currents in spinal dorsal horn neurones by the potent GABAB antagonist CGP55845
J F Blake, C Q Cao, P M Headley, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 31, 2000
Design, synthesis and biological evaluation of 3-amino-3-phenylpropionamide derivatives as novel mu opioid receptor ligands
M P Allen, J F Blake, D K Bryce, et al.
Journal of Medicinal Chemistry
|
November 22, 1996
Glucose transport-enhancing and hypoglycemic activity of 2-methyl-2-phenoxy-3-phenylpropanoic acids
R Sarges, R F Hank, J F Blake, et al.
Journal of Medicinal Chemistry
|
May 18, 2001
Quinazolin-4-one alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor antagonists: structure-activity relationship of the C-2 side chain tether
B L Chenard, W M Welch, J F Blake, et al.
Journal of Medicinal Chemistry
|
August 19, 1994
Novel benzisoxazole derivatives as potent and selective inhibitors of acetylcholinesterase
A Villalobos, J F Blake, C K Biggers, et al.
Journal of Medicinal Chemistry
|
July 6, 2000
Structure-based design and synthesis of a potent matrix metalloproteinase-13 inhibitor based on a pyrrolidinone scaffold
R P Robinson, E R Laird, J F Blake, et al.
Journal of Medicinal Chemistry
|
April 17, 1998
(3R,4S)-3-[4-(4-fluorophenyl)-4-hydroxypiperidin-1-yl]chroman-4,7-diol: a conformationally restricted analogue of the NR2B subtype-selective NMDA antagonist (1S,2S)-1-(4-hydroxyphenyl)-2-(4-hydroxy-4-phenylpiperidino)- 1-propanol
T W Butler, J F Blake, J Bordner, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 18, 1999
Inhibition of MMP-1 and MMP-13 with phosphinic acids that exploit binding in the S2 pocket
L A Reiter, J P Rizzi, J Pandit, et al.
Page
of 2