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

D L Boger

Showing results (21-30 of 85) with videos related to

Pageof 9
Sort By:
Bioorganic & Medicinal Chemistry|February 1, 1996
Synthesis and evaluation of potential N pi and N sigma metal chelation sites within the beta-hydroxy-L-histidine subunit of bleomycin A2: functional characterization of imidazole N pi metal complexationD L Boger, T M Ramsey, H Cai
Bioorganic & Medicinal Chemistry Letters|August 11, 2000
Synthesis and evaluation of aza HUN-7293D L Boger, Y Chen, C A Foster
Proceedings of the National Academy of Sciences of the United States of America|May 16, 1998
Structural requirements for 5-HT2A and 5-HT1A serotonin receptor potentiation by the biologically active lipid oleamideD L Boger, J E Patterson, Q Jin
Bioorganic & Medicinal Chemistry|June 1, 1995
CBI-CDPBO1 and CBI-CDPBI1: CC-1065 analogs containing deep-seated modifications in the DNA binding subunitD L Boger, W Yun, H Cai, et al.
The Journal of Organic Chemistry|July 21, 2001
Synthesis and evaluation of a series of C3-substituted CBI analogues of CC-1065 and the duocarmycinsD L Boger, S R Brunette, R M Garbaccio
The Journal of Organic Chemistry|April 3, 2001
Synthesis, chemical properties, and biological evaluation of CC-1065 and duocarmycin analogues incorporating the 5-methoxycarbonyl-1,2,9,9a-tetrahydrocyclopropaD L Boger, T V Hughes, M P Hedrick
Journal of the American Chemical Society|September 20, 2001
Metal cation complexation and activation of reversed CPyI analogues of CC-1065 and duocarmycin SA: partitioning the effects of binding and catalysisD A Ellis, S E Wolkenberg, D L Boger
Bioorganic & Medicinal Chemistry Letters|June 8, 2000
A new class of highly cytotoxic diketopiperazinesD L Boger, B E Fink, M P Hedrick
Current Pharmaceutical Design|April 10, 1999
Oleamide: an endogenous sleep-inducing lipid and prototypical member of a new class of biological signaling moleculesD L Boger, S J Henriksen, B F Cravatt
Bioorganic & Medicinal Chemistry Letters|April 1, 2000
Bifunctional alkylating agents derived from duocarmycin SA: potent antitumor activity with altered sequence selectivityD L Boger, M Searcey, W C Tse, et al.
Pageof 9

Showing results (21-30 of 85) with videos related to

Sort By:
Pageof 9
Bioorganic & Medicinal Chemistry|February 1, 1996
Synthesis and evaluation of potential N pi and N sigma metal chelation sites within the beta-hydroxy-L-histidine subunit of bleomycin A2: functional characterization of imidazole N pi metal complexationD L Boger, T M Ramsey, H Cai
Bioorganic & Medicinal Chemistry Letters|August 11, 2000
Synthesis and evaluation of aza HUN-7293D L Boger, Y Chen, C A Foster
Proceedings of the National Academy of Sciences of the United States of America|May 16, 1998
Structural requirements for 5-HT2A and 5-HT1A serotonin receptor potentiation by the biologically active lipid oleamideD L Boger, J E Patterson, Q Jin
Bioorganic & Medicinal Chemistry|June 1, 1995
CBI-CDPBO1 and CBI-CDPBI1: CC-1065 analogs containing deep-seated modifications in the DNA binding subunitD L Boger, W Yun, H Cai, et al.
The Journal of Organic Chemistry|July 21, 2001
Synthesis and evaluation of a series of C3-substituted CBI analogues of CC-1065 and the duocarmycinsD L Boger, S R Brunette, R M Garbaccio
The Journal of Organic Chemistry|April 3, 2001
Synthesis, chemical properties, and biological evaluation of CC-1065 and duocarmycin analogues incorporating the 5-methoxycarbonyl-1,2,9,9a-tetrahydrocyclopropaD L Boger, T V Hughes, M P Hedrick
Journal of the American Chemical Society|September 20, 2001
Metal cation complexation and activation of reversed CPyI analogues of CC-1065 and duocarmycin SA: partitioning the effects of binding and catalysisD A Ellis, S E Wolkenberg, D L Boger
Bioorganic & Medicinal Chemistry Letters|June 8, 2000
A new class of highly cytotoxic diketopiperazinesD L Boger, B E Fink, M P Hedrick
Current Pharmaceutical Design|April 10, 1999
Oleamide: an endogenous sleep-inducing lipid and prototypical member of a new class of biological signaling moleculesD L Boger, S J Henriksen, B F Cravatt
Bioorganic & Medicinal Chemistry Letters|April 1, 2000
Bifunctional alkylating agents derived from duocarmycin SA: potent antitumor activity with altered sequence selectivityD L Boger, M Searcey, W C Tse, et al.
Pageof 9