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Journal of Medicinal Chemistry
|
October 1, 1988
Synthesis and pharmacological characterization of 1-phenyl-, 4-phenyl-, and 1-benzyl-1,2,3,4-tetrahydroisoquinolines as dopamine receptor ligands
P S Charifson, S D Wyrick, A J Hoffman, et al.
Journal of Clinical Pharmacology
|
December 1, 1993
Computer-assisted molecular modeling: indispensable tools for molecular pharmacology
J P Bowen, P S Charifson, P C Fox, et al.
Chemistry & Biology
|
June 30, 2000
The structures of caspases-1, -3, -7 and -8 reveal the basis for substrate and inhibitor selectivity
Y Wei, T Fox, S P Chambers, et al.
Journal of Medicinal Chemistry
|
November 25, 1994
Conformational analysis, pharmacophore identification, and comparative molecular field analysis of ligands for the neuromodulatory sigma 3 receptor
A M Myers, P S Charifson, C E Owens, et al.
Biochemistry
|
May 27, 1997
Peptide ligands of pp60(c-src) SH2 domains: a thermodynamic and structural study
P S Charifson, L M Shewchuk, W Rocque, et al.
Journal of Medicinal Chemistry
|
June 20, 1998
Potent dipeptide inhibitors of the pp60c-src SH2 domain
G J Pacofsky, K Lackey, K J Alligood, et al.
Chemistry & Biology
|
March 7, 1998
Identification of peroxisome proliferator-activated receptor ligands from a biased chemical library
P J Brown, T A Smith-Oliver, P S Charifson, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 1, 1999
The formation of a covalent complex between a dipeptide ligand and the src SH2 domain
K J Alligood, P S Charifson, R Crosby, et al.
Journal of Medicinal Chemistry
|
December 4, 1998
N-(2-Benzoylphenyl)-L-tyrosine PPARgamma agonists. 3. Structure-activity relationship and optimization of the N-aryl substituent
J E Cobb, S G Blanchard, E G Boswell, et al.
Journal of Medicinal Chemistry
|
December 4, 1998
N-(2-Benzoylphenyl)-L-tyrosine PPARgamma agonists. 2. Structure-activity relationship and optimization of the phenyl alkyl ether moiety
J L Collins, S G Blanchard, G E Boswell, et al.
Page
of 2
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Showing results (11-20 of 20) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 20 results.
Journal of Medicinal Chemistry
|
October 1, 1988
Synthesis and pharmacological characterization of 1-phenyl-, 4-phenyl-, and 1-benzyl-1,2,3,4-tetrahydroisoquinolines as dopamine receptor ligands
P S Charifson, S D Wyrick, A J Hoffman, et al.
Journal of Clinical Pharmacology
|
December 1, 1993
Computer-assisted molecular modeling: indispensable tools for molecular pharmacology
J P Bowen, P S Charifson, P C Fox, et al.
Chemistry & Biology
|
June 30, 2000
The structures of caspases-1, -3, -7 and -8 reveal the basis for substrate and inhibitor selectivity
Y Wei, T Fox, S P Chambers, et al.
Journal of Medicinal Chemistry
|
November 25, 1994
Conformational analysis, pharmacophore identification, and comparative molecular field analysis of ligands for the neuromodulatory sigma 3 receptor
A M Myers, P S Charifson, C E Owens, et al.
Biochemistry
|
May 27, 1997
Peptide ligands of pp60(c-src) SH2 domains: a thermodynamic and structural study
P S Charifson, L M Shewchuk, W Rocque, et al.
Journal of Medicinal Chemistry
|
June 20, 1998
Potent dipeptide inhibitors of the pp60c-src SH2 domain
G J Pacofsky, K Lackey, K J Alligood, et al.
Chemistry & Biology
|
March 7, 1998
Identification of peroxisome proliferator-activated receptor ligands from a biased chemical library
P J Brown, T A Smith-Oliver, P S Charifson, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 1, 1999
The formation of a covalent complex between a dipeptide ligand and the src SH2 domain
K J Alligood, P S Charifson, R Crosby, et al.
Journal of Medicinal Chemistry
|
December 4, 1998
N-(2-Benzoylphenyl)-L-tyrosine PPARgamma agonists. 3. Structure-activity relationship and optimization of the N-aryl substituent
J E Cobb, S G Blanchard, E G Boswell, et al.
Journal of Medicinal Chemistry
|
December 4, 1998
N-(2-Benzoylphenyl)-L-tyrosine PPARgamma agonists. 2. Structure-activity relationship and optimization of the phenyl alkyl ether moiety
J L Collins, S G Blanchard, G E Boswell, et al.
Page
of 2