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

Mark P Thomas

Showing results (21-30 of 52) with videos related to

Pageof 6
Sort By:
ACS Omega|October 16, 2018
C-3- and C-4-Substituted Bicyclic Coumarin Sulfamates as Potent Steroid Sulfatase InhibitorsDharshini Ganeshapillai, L W Lawrence Woo, Mark P Thomas, et al.
Journal of Medicinal Chemistry|September 17, 2014
Cyclic adenosine 5'-diphosphate ribose analogs without a "southern" ribose inhibit ADP-ribosyl cyclase-hydrolase CD38Joanna M Swarbrick, Richard Graeff, Hongmin Zhang, et al.
Chemical Communications (Cambridge, England)|January 24, 2014
'Click cyclic ADP-ribose': a neutral second messenger mimicJoanna M Swarbrick, Richard Graeff, Clive Garnham, et al.
Biochemistry|January 30, 2008
Generation of nucleophilic character in the Cys25/His159 ion pair of papain involves Trp177 but not Asp158Sheraz Gul, Syeed Hussain, Mark P Thomas, et al.
Journal of Medicinal Chemistry|January 18, 2012
Aberrant cyclization affords a C-6 modified cyclic adenosine 5'-diphosphoribose analogue with biological activity in Jurkat T cellsChristelle Moreau, Tanja Kirchberger, Bo Zhang, et al.
Chemmedchem|March 16, 2013
Synthesis and structure-activity relationship studies of derivatives of the dual aromatase-sulfatase inhibitor 4-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-yl)amino]methyl}phenyl sulfamateL W Lawrence Woo, Paul M Wood, Christian Bubert, et al.
Chemmedchem|June 30, 2011
Adamantyl ethanone pyridyl derivatives: potent and selective inhibitors of human 11β-hydroxysteroid dehydrogenase type 1Xiangdong Su, Fabienne Pradaux-Caggiano, Nigel Vicker, et al.
Frontiers in Psychiatry|October 5, 2018
Synthesis, Biological Evaluation, and SAR Studies of 14β-phenylacetyl Substituted 17-cyclopropylmethyl-7, 8-dihydronoroxymorphinones Derivatives: Ligands With Mixed NOP and Opioid Receptor ProfileVinod Kumar, Willma E Polgar, Gerta Cami-Kobeci, et al.
Bioorganic & Medicinal Chemistry|October 9, 2012
Adamantyl carboxamides and acetamides as potent human 11β-hydroxysteroid dehydrogenase type 1 inhibitorsXiangdong Su, Heather A Halem, Mark P Thomas, et al.
The Journal of Organic Chemistry|February 27, 2013
Regioselective opening of myo-inositol orthoesters: mechanism and synthetic utilityHimali Y Godage, Andrew M Riley, Timothy J Woodman, et al.
Pageof 6

Showing results (21-30 of 52) with videos related to

Sort By:
Pageof 6
ACS Omega|October 16, 2018
C-3- and C-4-Substituted Bicyclic Coumarin Sulfamates as Potent Steroid Sulfatase InhibitorsDharshini Ganeshapillai, L W Lawrence Woo, Mark P Thomas, et al.
Journal of Medicinal Chemistry|September 17, 2014
Cyclic adenosine 5'-diphosphate ribose analogs without a "southern" ribose inhibit ADP-ribosyl cyclase-hydrolase CD38Joanna M Swarbrick, Richard Graeff, Hongmin Zhang, et al.
Chemical Communications (Cambridge, England)|January 24, 2014
'Click cyclic ADP-ribose': a neutral second messenger mimicJoanna M Swarbrick, Richard Graeff, Clive Garnham, et al.
Biochemistry|January 30, 2008
Generation of nucleophilic character in the Cys25/His159 ion pair of papain involves Trp177 but not Asp158Sheraz Gul, Syeed Hussain, Mark P Thomas, et al.
Journal of Medicinal Chemistry|January 18, 2012
Aberrant cyclization affords a C-6 modified cyclic adenosine 5'-diphosphoribose analogue with biological activity in Jurkat T cellsChristelle Moreau, Tanja Kirchberger, Bo Zhang, et al.
Chemmedchem|March 16, 2013
Synthesis and structure-activity relationship studies of derivatives of the dual aromatase-sulfatase inhibitor 4-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-yl)amino]methyl}phenyl sulfamateL W Lawrence Woo, Paul M Wood, Christian Bubert, et al.
Chemmedchem|June 30, 2011
Adamantyl ethanone pyridyl derivatives: potent and selective inhibitors of human 11β-hydroxysteroid dehydrogenase type 1Xiangdong Su, Fabienne Pradaux-Caggiano, Nigel Vicker, et al.
Frontiers in Psychiatry|October 5, 2018
Synthesis, Biological Evaluation, and SAR Studies of 14β-phenylacetyl Substituted 17-cyclopropylmethyl-7, 8-dihydronoroxymorphinones Derivatives: Ligands With Mixed NOP and Opioid Receptor ProfileVinod Kumar, Willma E Polgar, Gerta Cami-Kobeci, et al.
Bioorganic & Medicinal Chemistry|October 9, 2012
Adamantyl carboxamides and acetamides as potent human 11β-hydroxysteroid dehydrogenase type 1 inhibitorsXiangdong Su, Heather A Halem, Mark P Thomas, et al.
The Journal of Organic Chemistry|February 27, 2013
Regioselective opening of myo-inositol orthoesters: mechanism and synthetic utilityHimali Y Godage, Andrew M Riley, Timothy J Woodman, et al.
Pageof 6