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

P Krogsgaard-Larsen

Showing results (171-180 of 203) with videos related to

Pageof 21
Sort By:
Chirality|November 24, 1999
Resolution, absolute stereochemistry, and enantiopharmacology of the GluR1-4 and GluR5 antagonist 2-amino-3-[5-tert-butyl-3-(phosphonomethoxy)-4-isoxazolyl]propionic acidE H Møller, J Egebjerg, L Brehm, et al.
European Journal of Pharmacology|February 13, 2001
Stereochemistry and molecular pharmacology of (S)-thio-ATPA, a new potent and selective GluR5 agonistT B Stensbøl, H S Jensen, B Nielsen, et al.
Journal of Medicinal Chemistry|June 1, 1983
4,5,6,7-Tetrahydroisothiazolo[5,4-c]pyridin-3-ol and related analogues of THIP. Synthesis and biological activityP Krogsgaard-Larsen, H Mikkelsen, P Jacobsen, et al.
European Journal of Pharmacology|December 15, 1990
NMDA receptor agonists derived from ibotenic acid. Preparation, neuroexcitation and neurotoxicityU Madsen, J W Ferkany, B E Jones, et al.
Drug Design and Delivery|May 1, 1987
Synthesis and biological activity of a GABAA agonist which has no effect on benzodiazepine binding and of structurally related glycine antagonistsJ R Byberg, I M Labouta, E Falch, et al.
Bioorganic & Medicinal Chemistry|May 17, 2001
Synthesis and receptor binding affinity of new selective GluR5 ligandsL Bunch, T H Johansen, H Bräuner-Osborne, et al.
Journal of Medicinal Chemistry|December 22, 2000
Structural determinants of AMPA agonist activity in analogues of 2-amino-3-(3-carboxy-5-methyl-4-isoxazolyl)propionic acid: synthesis and pharmacologyB Bang-Andersen, H Ahmadian, S M Lenz, et al.
Journal of Medicinal Chemistry|April 1, 1994
Resolution, absolute stereochemistry, and pharmacology of the S-(+)- and R-(-)-isomers of the apparent partial AMPA receptor agonist (R,S)-2-amino-3-(3-hydroxy-5-phenylisoxazol-4-yl)propionic acid [(R,S)-APPA]B Ebert, S Lenz, L Brehm, et al.
Journal of Medicinal Chemistry|April 12, 1996
Synthesis and pharmacology of highly selective carboxy and phosphono isoxazole amino acid AMPA receptor antagonistsU Madsen, B Bang-Andersen, L Brehm, et al.
Journal of Medicinal Chemistry|July 3, 1998
Heteroaryl analogues of AMPA. 2. Synthesis, absolute stereochemistry, photochemistry, and structure-activity relationshipsE Falch, L Brehm, I Mikkelsen, et al.
Pageof 21

Showing results (171-180 of 203) with videos related to

Sort By:
Pageof 21
Chirality|November 24, 1999
Resolution, absolute stereochemistry, and enantiopharmacology of the GluR1-4 and GluR5 antagonist 2-amino-3-[5-tert-butyl-3-(phosphonomethoxy)-4-isoxazolyl]propionic acidE H Møller, J Egebjerg, L Brehm, et al.
European Journal of Pharmacology|February 13, 2001
Stereochemistry and molecular pharmacology of (S)-thio-ATPA, a new potent and selective GluR5 agonistT B Stensbøl, H S Jensen, B Nielsen, et al.
Journal of Medicinal Chemistry|June 1, 1983
4,5,6,7-Tetrahydroisothiazolo[5,4-c]pyridin-3-ol and related analogues of THIP. Synthesis and biological activityP Krogsgaard-Larsen, H Mikkelsen, P Jacobsen, et al.
European Journal of Pharmacology|December 15, 1990
NMDA receptor agonists derived from ibotenic acid. Preparation, neuroexcitation and neurotoxicityU Madsen, J W Ferkany, B E Jones, et al.
Drug Design and Delivery|May 1, 1987
Synthesis and biological activity of a GABAA agonist which has no effect on benzodiazepine binding and of structurally related glycine antagonistsJ R Byberg, I M Labouta, E Falch, et al.
Bioorganic & Medicinal Chemistry|May 17, 2001
Synthesis and receptor binding affinity of new selective GluR5 ligandsL Bunch, T H Johansen, H Bräuner-Osborne, et al.
Journal of Medicinal Chemistry|December 22, 2000
Structural determinants of AMPA agonist activity in analogues of 2-amino-3-(3-carboxy-5-methyl-4-isoxazolyl)propionic acid: synthesis and pharmacologyB Bang-Andersen, H Ahmadian, S M Lenz, et al.
Journal of Medicinal Chemistry|April 1, 1994
Resolution, absolute stereochemistry, and pharmacology of the S-(+)- and R-(-)-isomers of the apparent partial AMPA receptor agonist (R,S)-2-amino-3-(3-hydroxy-5-phenylisoxazol-4-yl)propionic acid [(R,S)-APPA]B Ebert, S Lenz, L Brehm, et al.
Journal of Medicinal Chemistry|April 12, 1996
Synthesis and pharmacology of highly selective carboxy and phosphono isoxazole amino acid AMPA receptor antagonistsU Madsen, B Bang-Andersen, L Brehm, et al.
Journal of Medicinal Chemistry|July 3, 1998
Heteroaryl analogues of AMPA. 2. Synthesis, absolute stereochemistry, photochemistry, and structure-activity relationshipsE Falch, L Brehm, I Mikkelsen, et al.
Pageof 21