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Rhona J Cox

Showing results (1-10 of 13) with videos related to

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Journal of Medicinal Chemistry|November 5, 2015
Small Molecule CXCR3 AntagonistsStephen P Andrews, Rhona J Cox
Accounts of Chemical Research|February 19, 2003
Paraherquamides, brevianamides, and asperparalines: laboratory synthesis and biosynthesis. An interim reportRobert M Williams, Rhona J Cox
Drug Metabolism and Disposition: the Biological Fate of Chemicals|May 23, 2019
Plasma Protein Binding as an Optimizable Parameter for Acidic DrugsPhilip Gardiner, Rhona J Cox, Ken Grime
Future Medicinal Chemistry|April 21, 2021
The powerful symbiosis between synthetic and medicinal chemistryStefan Schiesser, Rhona J Cox, Werngard Czechtizky
Journal of the American Chemical Society|October 2, 2003
Asymmetric, stereocontrolled total synthesis of paraherquamide ARobert M Williams, Jianhua Cao, Hidekazu Tsujishima, et al.
Journal of Medicinal Chemistry|October 28, 2020
<i>N</i>-Trifluoromethyl Amines and Azoles: An Underexplored Functional Group in the Medicinal Chemist's ToolboxStefan Schiesser, Hanna Chepliaka, Johanna Kollback, et al.
Progress in Medicinal Chemistry|June 26, 2022
Advances in the design of new types of inhaled medicinesWerngard Czechtizky, Wu Su, Lena Ripa, et al.
European Journal of Medicinal Chemistry|November 6, 2021
Discovery and optimization of cyclohexane-1,4-diamines as allosteric MALT1 inhibitorsStefan Schiesser, Peter Hajek, Huw E Pople, et al.
Organic Letters|September 4, 2007
The first synthesis of the ABC-ring system of 'upenamideJan Peter Schmidt, Sandra Beltrán-Rodil, Rhona J Cox, et al.
Plos One|September 2, 2020
A MALT1 inhibitor suppresses human myeloid DC, effector T-cell and B-cell responses and retains Th1/regulatory T-cell homeostasisCeline Dumont, Ulf Sivars, Theresa Andreasson, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Journal of Medicinal Chemistry|November 5, 2015
Small Molecule CXCR3 AntagonistsStephen P Andrews, Rhona J Cox
Accounts of Chemical Research|February 19, 2003
Paraherquamides, brevianamides, and asperparalines: laboratory synthesis and biosynthesis. An interim reportRobert M Williams, Rhona J Cox
Drug Metabolism and Disposition: the Biological Fate of Chemicals|May 23, 2019
Plasma Protein Binding as an Optimizable Parameter for Acidic DrugsPhilip Gardiner, Rhona J Cox, Ken Grime
Future Medicinal Chemistry|April 21, 2021
The powerful symbiosis between synthetic and medicinal chemistryStefan Schiesser, Rhona J Cox, Werngard Czechtizky
Journal of the American Chemical Society|October 2, 2003
Asymmetric, stereocontrolled total synthesis of paraherquamide ARobert M Williams, Jianhua Cao, Hidekazu Tsujishima, et al.
Journal of Medicinal Chemistry|October 28, 2020
<i>N</i>-Trifluoromethyl Amines and Azoles: An Underexplored Functional Group in the Medicinal Chemist's ToolboxStefan Schiesser, Hanna Chepliaka, Johanna Kollback, et al.
Progress in Medicinal Chemistry|June 26, 2022
Advances in the design of new types of inhaled medicinesWerngard Czechtizky, Wu Su, Lena Ripa, et al.
European Journal of Medicinal Chemistry|November 6, 2021
Discovery and optimization of cyclohexane-1,4-diamines as allosteric MALT1 inhibitorsStefan Schiesser, Peter Hajek, Huw E Pople, et al.
Organic Letters|September 4, 2007
The first synthesis of the ABC-ring system of 'upenamideJan Peter Schmidt, Sandra Beltrán-Rodil, Rhona J Cox, et al.
Plos One|September 2, 2020
A MALT1 inhibitor suppresses human myeloid DC, effector T-cell and B-cell responses and retains Th1/regulatory T-cell homeostasisCeline Dumont, Ulf Sivars, Theresa Andreasson, et al.
Pageof 2