Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

C F Bigge

Showing results (1-10 of 14) with videos related to

Pageof 2
Sort By:
Current Opinion in Chemical Biology|July 27, 1999
Ionotropic glutamate receptorsC F Bigge
Journal of Medicinal Chemistry|July 1, 1983
5-p-benzoquinonyl-2'-deoxyuridine 5'-phosphate: a possible mechanism-based inhibitor of thymidylate synthetaseL Maggiora, C T Chang, M E Hasson, et al.
Stroke|July 2, 1999
The neuroprotective effect of the novel AMPA receptor antagonist PD152247 (PNQX) in temporary focal ischemia in the ratG P Schielke, N C Kupina, P A Boxer, et al.
Journal of Medicinal Chemistry|May 26, 1995
Potent, orally active, competitive N-methyl-D-aspartate (NMDA) receptor antagonists are substrates for a neutral amino acid uptake system in Chinese hamster ovary cellsJ H Li, C F Bigge, R M Williamson, et al.
Journal of Medicinal Chemistry|April 17, 1992
Generation of N-methyl-D-aspartate agonist and competitive antagonist pharmacophore models. Design and synthesis of phosphonoalkyl-substituted tetrahydroisoquinolines as novel antagonistsD F Ortwine, T C Malone, C F Bigge, et al.
Journal of Medicinal Chemistry|July 1, 1989
Exploration of phenyl-spaced 2-amino-(5-9)-phosphonoalkanoic acids as competitive N-methyl-D-aspartic acid antagonistsC F Bigge, J T Drummond, G Johnson, et al.
Pharmaceutical Research|April 23, 1999
Evidence for overlapping substrate specificity between large neutral amino acid (LNAA) and dipeptide (hPEPT1) transporters for PD 158473, an NMDA antagonistN Surendran, K M Covitz, H Han, et al.
Journal of Medicinal Chemistry|April 27, 1992
Exploration of N-phosphonoalkyl-, N-phosphonoalkenyl-, and N-(phosphonoalkyl)phenyl-spaced alpha-amino acids as competitive N-methyl-D-aspartic acid antagonistsC F Bigge, G Johnson, D F Ortwine, et al.
Journal of Medicinal Chemistry|October 1, 1990
New and versatile approaches to the synthesis of CPP-related competitive NMDA antagonists. Preliminary structure-activity relationships and pharmacological evaluationS J Hays, C F Bigge, P M Novak, et al.
Journal of Medicinal Chemistry|March 19, 1993
Synthesis and pharmacological evaluation of hexahydrofluorenamines as noncompetitive antagonists at the N-methyl-D-aspartate receptorS J Hays, P M Novak, D F Ortwine, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Current Opinion in Chemical Biology|July 27, 1999
Ionotropic glutamate receptorsC F Bigge
Journal of Medicinal Chemistry|July 1, 1983
5-p-benzoquinonyl-2'-deoxyuridine 5'-phosphate: a possible mechanism-based inhibitor of thymidylate synthetaseL Maggiora, C T Chang, M E Hasson, et al.
Stroke|July 2, 1999
The neuroprotective effect of the novel AMPA receptor antagonist PD152247 (PNQX) in temporary focal ischemia in the ratG P Schielke, N C Kupina, P A Boxer, et al.
Journal of Medicinal Chemistry|May 26, 1995
Potent, orally active, competitive N-methyl-D-aspartate (NMDA) receptor antagonists are substrates for a neutral amino acid uptake system in Chinese hamster ovary cellsJ H Li, C F Bigge, R M Williamson, et al.
Journal of Medicinal Chemistry|April 17, 1992
Generation of N-methyl-D-aspartate agonist and competitive antagonist pharmacophore models. Design and synthesis of phosphonoalkyl-substituted tetrahydroisoquinolines as novel antagonistsD F Ortwine, T C Malone, C F Bigge, et al.
Journal of Medicinal Chemistry|July 1, 1989
Exploration of phenyl-spaced 2-amino-(5-9)-phosphonoalkanoic acids as competitive N-methyl-D-aspartic acid antagonistsC F Bigge, J T Drummond, G Johnson, et al.
Pharmaceutical Research|April 23, 1999
Evidence for overlapping substrate specificity between large neutral amino acid (LNAA) and dipeptide (hPEPT1) transporters for PD 158473, an NMDA antagonistN Surendran, K M Covitz, H Han, et al.
Journal of Medicinal Chemistry|April 27, 1992
Exploration of N-phosphonoalkyl-, N-phosphonoalkenyl-, and N-(phosphonoalkyl)phenyl-spaced alpha-amino acids as competitive N-methyl-D-aspartic acid antagonistsC F Bigge, G Johnson, D F Ortwine, et al.
Journal of Medicinal Chemistry|October 1, 1990
New and versatile approaches to the synthesis of CPP-related competitive NMDA antagonists. Preliminary structure-activity relationships and pharmacological evaluationS J Hays, C F Bigge, P M Novak, et al.
Journal of Medicinal Chemistry|March 19, 1993
Synthesis and pharmacological evaluation of hexahydrofluorenamines as noncompetitive antagonists at the N-methyl-D-aspartate receptorS J Hays, P M Novak, D F Ortwine, et al.
Pageof 2