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

H G Capraro

Showing results (11-20 of 14) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 14 results.
Journal of Medicinal Chemistry|March 1, 1981
Biological effects of modified colchicines. Improved preparation of 2-demethylcolchicine, 3-demethylcolchicine, and (+)-colchicine and reassignment of the position of the double bond in dehydro-7-deacetamidocolchicinesM Rösner, H G Capraro, A E Jacobson, et al.
Archiv Der Pharmazie|June 1, 1996
Synthesis of potent and orally active HIV-protease inhibitorsH G Capraro, G Bold, A Fässler, et al.
Schweizerische Medizinische Wochenschrift|October 26, 1996
Profile of CGP 61755: a novel and potent HIV-1 protease inhibitor that shows enhanced anti-HIV activity when combined with other antiretroviral agents in vitroJ K Lazdins, G Bold, H G Capraro, et al.
Journal of Medicinal Chemistry|August 28, 1998
New aza-dipeptide analogues as potent and orally absorbed HIV-1 protease inhibitors: candidates for clinical developmentG Bold, A Fässler, H G Capraro, et al.
Pageof 2

Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Journal of Medicinal Chemistry|March 1, 1981
Biological effects of modified colchicines. Improved preparation of 2-demethylcolchicine, 3-demethylcolchicine, and (+)-colchicine and reassignment of the position of the double bond in dehydro-7-deacetamidocolchicinesM Rösner, H G Capraro, A E Jacobson, et al.
Archiv Der Pharmazie|June 1, 1996
Synthesis of potent and orally active HIV-protease inhibitorsH G Capraro, G Bold, A Fässler, et al.
Schweizerische Medizinische Wochenschrift|October 26, 1996
Profile of CGP 61755: a novel and potent HIV-1 protease inhibitor that shows enhanced anti-HIV activity when combined with other antiretroviral agents in vitroJ K Lazdins, G Bold, H G Capraro, et al.
Journal of Medicinal Chemistry|August 28, 1998
New aza-dipeptide analogues as potent and orally absorbed HIV-1 protease inhibitors: candidates for clinical developmentG Bold, A Fässler, H G Capraro, et al.
Pageof 2