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

Daniel Conole

Showing results (21-30 of 32) with videos related to

Pageof 4
Sort By:
Journal of Medicinal Chemistry|March 13, 2024
Structure-Guided Design and Optimization of Covalent VHL-Targeted Sulfonyl Fluoride PROTACsRishi R Shah, Elena De Vita, Preethi S Sathyamurthi, et al.
Bioorganic & Medicinal Chemistry|February 23, 2019
Structure-activity relationships for unit C pyridyl analogues of the tuberculosis drug bedaquilineAdrian Blaser, Hamish S Sutherland, Amy S T Tong, et al.
Bioorganic & Medicinal Chemistry|February 28, 2018
Structure-activity relationships for analogs of the tuberculosis drug bedaquiline with the naphthalene unit replaced by bicyclic heterocyclesHamish S Sutherland, Amy S T Tong, Peter J Choi, et al.
European Journal of Medicinal Chemistry|December 28, 2021
Synthesis and structure-activity relationships for a new class of tetrahydronaphthalene amide inhibitors of Mycobacterium tuberculosisHamish S Sutherland, Guo-Liang Lu, Amy S T Tong, et al.
Bioorganic & Medicinal Chemistry|February 27, 2019
3,5-Dialkoxypyridine analogues of bedaquiline are potent antituberculosis agents with minimal inhibition of the hERG channelHamish S Sutherland, Amy S T Tong, Peter J Choi, et al.
Bioorganic & Medicinal Chemistry|June 30, 2022
Structure-activity relationships of 2-pyrimidinecarbohydrazides as utrophin modulators for the potential treatment of Duchenne muscular dystrophyMaria Chatzopoulou, Daniel Conole, Enrico Emer, et al.
Bioorganic & Medicinal Chemistry|October 2, 2020
Synthesis and structure-activity relationships for tetrahydroisoquinoline-based inhibitors of Mycobacterium tuberculosisGuo-Liang Lu, Amy S T Tong, Daniel Conole, et al.
ACS Medicinal Chemistry Letters|October 24, 2017
6-Cyano Analogues of Bedaquiline as Less Lipophilic and Potentially Safer Diarylquinolines for TuberculosisAmy S T Tong, Peter J Choi, Adrian Blaser, et al.
Chemical Communications (Cambridge, England)|September 6, 2022
Light-mediated multi-target protein degradation using arylazopyrazole photoswitchable PROTACs (AP-PROTACs)Qisi Zhang, Cyrille S Kounde, Milon Mondal, et al.
Oncogene|May 31, 2020
Targeting STAT3 signaling using stabilised sulforaphane (SFX-01) inhibits endocrine resistant stem-like cells in ER-positive breast cancerBruno M Simões, Angélica Santiago-Gómez, Chiara Chiodo, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
Journal of Medicinal Chemistry|March 13, 2024
Structure-Guided Design and Optimization of Covalent VHL-Targeted Sulfonyl Fluoride PROTACsRishi R Shah, Elena De Vita, Preethi S Sathyamurthi, et al.
Bioorganic & Medicinal Chemistry|February 23, 2019
Structure-activity relationships for unit C pyridyl analogues of the tuberculosis drug bedaquilineAdrian Blaser, Hamish S Sutherland, Amy S T Tong, et al.
Bioorganic & Medicinal Chemistry|February 28, 2018
Structure-activity relationships for analogs of the tuberculosis drug bedaquiline with the naphthalene unit replaced by bicyclic heterocyclesHamish S Sutherland, Amy S T Tong, Peter J Choi, et al.
European Journal of Medicinal Chemistry|December 28, 2021
Synthesis and structure-activity relationships for a new class of tetrahydronaphthalene amide inhibitors of Mycobacterium tuberculosisHamish S Sutherland, Guo-Liang Lu, Amy S T Tong, et al.
Bioorganic & Medicinal Chemistry|February 27, 2019
3,5-Dialkoxypyridine analogues of bedaquiline are potent antituberculosis agents with minimal inhibition of the hERG channelHamish S Sutherland, Amy S T Tong, Peter J Choi, et al.
Bioorganic & Medicinal Chemistry|June 30, 2022
Structure-activity relationships of 2-pyrimidinecarbohydrazides as utrophin modulators for the potential treatment of Duchenne muscular dystrophyMaria Chatzopoulou, Daniel Conole, Enrico Emer, et al.
Bioorganic & Medicinal Chemistry|October 2, 2020
Synthesis and structure-activity relationships for tetrahydroisoquinoline-based inhibitors of Mycobacterium tuberculosisGuo-Liang Lu, Amy S T Tong, Daniel Conole, et al.
ACS Medicinal Chemistry Letters|October 24, 2017
6-Cyano Analogues of Bedaquiline as Less Lipophilic and Potentially Safer Diarylquinolines for TuberculosisAmy S T Tong, Peter J Choi, Adrian Blaser, et al.
Chemical Communications (Cambridge, England)|September 6, 2022
Light-mediated multi-target protein degradation using arylazopyrazole photoswitchable PROTACs (AP-PROTACs)Qisi Zhang, Cyrille S Kounde, Milon Mondal, et al.
Oncogene|May 31, 2020
Targeting STAT3 signaling using stabilised sulforaphane (SFX-01) inhibits endocrine resistant stem-like cells in ER-positive breast cancerBruno M Simões, Angélica Santiago-Gómez, Chiara Chiodo, et al.
Pageof 4