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

R A Tommasi

Showing results (1-10 of 4) with videos related to

Pageof 1
Sort By:
Bioorganic & Medicinal Chemistry Letters|January 1, 1999
Non-peptidic HIV protease inhibitors: C2-symmetry-based design of bis-sulfonamide dihydropyronesM N Janakiraman, K D Watenpaugh, P K Tomich, et al.
Journal of Medicinal Chemistry|August 28, 1998
Tipranavir (PNU-140690): a potent, orally bioavailable nonpeptidic HIV protease inhibitor of the 5,6-dihydro-4-hydroxy-2-pyrone sulfonamide classS R Turner, J W Strohbach, R A Tommasi, et al.
Journal of Medicinal Chemistry|November 8, 1996
Structure-based design of HIV protease inhibitors: 5,6-dihydro-4-hydroxy-2-pyrones as effective, nonpeptidic inhibitorsS Thaisrivongs, D L Romero, R A Tommasi, et al.
Journal of Medicinal Chemistry|December 14, 2001
Identification of dipeptidyl nitriles as potent and selective inhibitors of cathepsin B through structure-based drug designP D Greenspan, K L Clark, R A Tommasi, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Bioorganic & Medicinal Chemistry Letters|January 1, 1999
Non-peptidic HIV protease inhibitors: C2-symmetry-based design of bis-sulfonamide dihydropyronesM N Janakiraman, K D Watenpaugh, P K Tomich, et al.
Journal of Medicinal Chemistry|August 28, 1998
Tipranavir (PNU-140690): a potent, orally bioavailable nonpeptidic HIV protease inhibitor of the 5,6-dihydro-4-hydroxy-2-pyrone sulfonamide classS R Turner, J W Strohbach, R A Tommasi, et al.
Journal of Medicinal Chemistry|November 8, 1996
Structure-based design of HIV protease inhibitors: 5,6-dihydro-4-hydroxy-2-pyrones as effective, nonpeptidic inhibitorsS Thaisrivongs, D L Romero, R A Tommasi, et al.
Journal of Medicinal Chemistry|December 14, 2001
Identification of dipeptidyl nitriles as potent and selective inhibitors of cathepsin B through structure-based drug designP D Greenspan, K L Clark, R A Tommasi, et al.
Pageof 1