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

T Sunazuka

Showing results (31-40 of 45) with videos related to

Pageof 5
Sort By:
The Journal of Antibiotics|March 21, 2000
Arisugacins C and D, novel acetylcholinesterase inhibitors and their related novel metabolites produced by Penicilium sp. FO-4259-11K Otoguro, K Shiomi, Y Yamaguchi, et al.
The Journal of Antibiotics|July 1, 1995
Structure-activity relationships of lactacystin, the first non-protein neurotrophic factorT Nagamitsu, T Sunazuka, H Stump, et al.
The Journal of Antibiotics|June 24, 2000
Synthesis and antiangiogenic activity of staurosporine derivativesZ Li, T Sunazuka, R Yamada, et al.
The Journal of Antibiotics|May 1, 1996
Andrastins A-C, new protein farnesyltransferase inhibitors produced by Penicillium sp. FO-3929. II. Structure elucidation and biosynthesisR Uchida, K Shiomi, J Inokoshi, et al.
The Journal of Antibiotics|November 1, 1996
Chemical modification and structure-activity relationships of pyripyropenes. 1. Modification at the four hydroxyl groupsR Obata, T Sunazuka, Z Li, et al.
The Journal of Antibiotics|January 2, 2001
Reversal of multidrug resistance by 7-O-benzoylpyripyropene A in multidrug-resistant tumor cellsM C Rho, M Hayashi, A Fukami, et al.
The Journal of Antibiotics|July 1, 1996
Chlovalicin, a new cytocidal antibiotic produced by Sporothrix sp. FO-4649. II. Physicochemical properties and structural elucidationS Takamatsu, Y P Kim, T Komiya, et al.
The Journal of Antibiotics|September 1, 1996
Kurasoins A and B, new protein farnesyltransferase inhibitors produced by Paecilomyces sp. FO-3684. II. Structure elucidation and total synthesisR Uchida, K Shiomi, T Sunazuka, et al.
Biochemical and Biophysical Research Communications|January 7, 2000
Erythromycin suppresses nuclear factor-kappaB and activator protein-1 activation in human bronchial epithelial cellsM Desaki, H Takizawa, T Ohtoshi, et al.
Chemical & Pharmaceutical Bulletin|March 1, 1994
Synthesis and biological activity of new 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) synthase inhibitors: 2-oxetanones with a side chain mimicking the folded structure of 1233AH Hashizume, H Ito, K Yamada, et al.
Pageof 5

Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
The Journal of Antibiotics|March 21, 2000
Arisugacins C and D, novel acetylcholinesterase inhibitors and their related novel metabolites produced by Penicilium sp. FO-4259-11K Otoguro, K Shiomi, Y Yamaguchi, et al.
The Journal of Antibiotics|July 1, 1995
Structure-activity relationships of lactacystin, the first non-protein neurotrophic factorT Nagamitsu, T Sunazuka, H Stump, et al.
The Journal of Antibiotics|June 24, 2000
Synthesis and antiangiogenic activity of staurosporine derivativesZ Li, T Sunazuka, R Yamada, et al.
The Journal of Antibiotics|May 1, 1996
Andrastins A-C, new protein farnesyltransferase inhibitors produced by Penicillium sp. FO-3929. II. Structure elucidation and biosynthesisR Uchida, K Shiomi, J Inokoshi, et al.
The Journal of Antibiotics|November 1, 1996
Chemical modification and structure-activity relationships of pyripyropenes. 1. Modification at the four hydroxyl groupsR Obata, T Sunazuka, Z Li, et al.
The Journal of Antibiotics|January 2, 2001
Reversal of multidrug resistance by 7-O-benzoylpyripyropene A in multidrug-resistant tumor cellsM C Rho, M Hayashi, A Fukami, et al.
The Journal of Antibiotics|July 1, 1996
Chlovalicin, a new cytocidal antibiotic produced by Sporothrix sp. FO-4649. II. Physicochemical properties and structural elucidationS Takamatsu, Y P Kim, T Komiya, et al.
The Journal of Antibiotics|September 1, 1996
Kurasoins A and B, new protein farnesyltransferase inhibitors produced by Paecilomyces sp. FO-3684. II. Structure elucidation and total synthesisR Uchida, K Shiomi, T Sunazuka, et al.
Biochemical and Biophysical Research Communications|January 7, 2000
Erythromycin suppresses nuclear factor-kappaB and activator protein-1 activation in human bronchial epithelial cellsM Desaki, H Takizawa, T Ohtoshi, et al.
Chemical & Pharmaceutical Bulletin|March 1, 1994
Synthesis and biological activity of new 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) synthase inhibitors: 2-oxetanones with a side chain mimicking the folded structure of 1233AH Hashizume, H Ito, K Yamada, et al.
Pageof 5