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

J P Burkhart

Showing results (1-10 of 12) with videos related to

Pageof 2
Sort By:
The Journal of Steroid Biochemistry and Molecular Biology|March 1, 1993
A-ring bridged steroids as potent inhibitors of aromataseN P Peet, J O Johnston, J P Burkhart, et al.
Steroids|March 1, 1985
Novel silylated steroids as aromatase inhibitorsJ P Burkhart, P M Weintraub, C L Wright, et al.
The Journal of Steroid Biochemistry and Molecular Biology|March 1, 1993
Biological characterization of A-ring steroidsJ O Johnston, C L Wright, J P Burkhart, et al.
Bioorganic & Medicinal Chemistry|September 1, 1996
Inhibition of steroid C17(20) lyase with C-17-heteroaryl steroidsJ P Burkhart, C A Gates, M E Laughlin, et al.
Biochemical and Biophysical Research Communications|January 30, 1990
The inhibition of human neutrophil elastase and cathepsin G by peptidyl 1,2-dicarbonyl derivativesS Mehdi, M R Angelastro, J P Burkhart, et al.
Bioorganic & Medicinal Chemistry Letters|January 1, 1999
Preparation of alpha-keto ester enol acetates as potential prodrugs of human neutrophil elastase inhibitorsJ P Burkhart, S Mehdi, J R Koehl, et al.
Journal of Medicinal Chemistry|January 1, 1990
Synthesis of peptidyl fluoromethyl ketones and peptidyl alpha-keto esters as inhibitors of porcine pancreatic elastase, human neutrophil elastase, and rat and human neutrophil cathepsin GN P Peet, J P Burkhart, M R Angelastro, et al.
The Journal of Pharmacology and Experimental Therapeutics|July 1, 1994
Pharmacology of N-[4-(4-morpholinylcarbonyl)benzoyl]-L-valyl-N- [3,3,4,4,4-pentafluoro-1-(1-methylethyl)-2-oxobutyl]-L-prolinamide (MDL 101,146): a potent orally active inhibitor of human neutrophil elastaseS L Durham, C M Hare, M R Angelastro, et al.
Biochemistry|February 4, 1997
Molecular design and characterization of an alpha-thrombin inhibitor containing a novel P1 moietyJ A Malikayil, J P Burkhart, H A Schreuder, et al.
Journal of Medicinal Chemistry|January 20, 1995
Inhibition of human neutrophil elastase. 3. An orally active enol acetate prodrugJ P Burkhart, J R Koehl, S Mehdi, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
The Journal of Steroid Biochemistry and Molecular Biology|March 1, 1993
A-ring bridged steroids as potent inhibitors of aromataseN P Peet, J O Johnston, J P Burkhart, et al.
Steroids|March 1, 1985
Novel silylated steroids as aromatase inhibitorsJ P Burkhart, P M Weintraub, C L Wright, et al.
The Journal of Steroid Biochemistry and Molecular Biology|March 1, 1993
Biological characterization of A-ring steroidsJ O Johnston, C L Wright, J P Burkhart, et al.
Bioorganic & Medicinal Chemistry|September 1, 1996
Inhibition of steroid C17(20) lyase with C-17-heteroaryl steroidsJ P Burkhart, C A Gates, M E Laughlin, et al.
Biochemical and Biophysical Research Communications|January 30, 1990
The inhibition of human neutrophil elastase and cathepsin G by peptidyl 1,2-dicarbonyl derivativesS Mehdi, M R Angelastro, J P Burkhart, et al.
Bioorganic & Medicinal Chemistry Letters|January 1, 1999
Preparation of alpha-keto ester enol acetates as potential prodrugs of human neutrophil elastase inhibitorsJ P Burkhart, S Mehdi, J R Koehl, et al.
Journal of Medicinal Chemistry|January 1, 1990
Synthesis of peptidyl fluoromethyl ketones and peptidyl alpha-keto esters as inhibitors of porcine pancreatic elastase, human neutrophil elastase, and rat and human neutrophil cathepsin GN P Peet, J P Burkhart, M R Angelastro, et al.
The Journal of Pharmacology and Experimental Therapeutics|July 1, 1994
Pharmacology of N-[4-(4-morpholinylcarbonyl)benzoyl]-L-valyl-N- [3,3,4,4,4-pentafluoro-1-(1-methylethyl)-2-oxobutyl]-L-prolinamide (MDL 101,146): a potent orally active inhibitor of human neutrophil elastaseS L Durham, C M Hare, M R Angelastro, et al.
Biochemistry|February 4, 1997
Molecular design and characterization of an alpha-thrombin inhibitor containing a novel P1 moietyJ A Malikayil, J P Burkhart, H A Schreuder, et al.
Journal of Medicinal Chemistry|January 20, 1995
Inhibition of human neutrophil elastase. 3. An orally active enol acetate prodrugJ P Burkhart, J R Koehl, S Mehdi, et al.
Pageof 2