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Kenneth A Jacobson

Showing results (581-590 of 599) with videos related to

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Journal of Medicinal Chemistry|January 25, 2014
Synthesis and anti-renal fibrosis activity of conformationally locked truncated 2-hexynyl-N(6)-substituted-(N)-methanocarba-nucleosides as A3 adenosine receptor antagonists and partial agonistsAkshata Nayak, Girish Chandra, Inah Hwang, et al.
ACS Chemical Neuroscience|September 1, 2021
Discovery of Highly Potent Adenosine A<sub>1</sub> Receptor Agonists: Targeting Positron Emission Tomography ProbesMin Guo, Abolghasem Bakhoda, Zhan-Guo Gao, et al.
Pain|May 8, 2020
Acute visceral pain relief mediated by A3AR agonists in rats: involvement of N-type voltage-gated calcium channelsElena Lucarini, Elisabetta Coppi, Laura Micheli, et al.
ACS Pharmacology & Translational Science|September 19, 2025
P2Y<sub>14</sub> Receptor Antagonists: Piperidine Bioisosteres and Mutagenesis-Supported Molecular ModelingAsmita Pramanik, Zhiwei Wen, Matteo Pavan, et al.
Ophthalmology|March 23, 2010
Treatment of dry eye syndrome with orally administered CF101: data from a phase 2 clinical trialIsaac Avni, Hanna J Garzozi, Irina S Barequet, et al.
Nature Chemistry|October 19, 2023
Stereocontrolled access to thioisosteres of nucleoside di- and triphosphatesHai-Jun Zhang, Michał Ociepa, Molhm Nassir, et al.
Journal of Medicinal Chemistry|December 7, 2011
Structure-activity relationships of truncated C2- or C8-substituted adenosine derivatives as dual acting A₂A and A₃ adenosine receptor ligandsXiyan Hou, Mahesh S Majik, Kyunglim Kim, et al.
Nature|March 28, 2014
Structure of the human P2Y12 receptor in complex with an antithrombotic drugKaihua Zhang, Jin Zhang, Zhan-Guo Gao, et al.
Journal of Medicinal Chemistry|August 21, 2023
Structure-Activity Relationship of Truncated 2,8-Disubstituted-Adenosine Derivatives as Dual A<sub>2A</sub>/A<sub>3</sub> Adenosine Receptor Antagonists and Their Cancer Immunotherapeutic ActivityGibae Kim, Xiyan Hou, Woong Sub Byun, et al.
Journal of Medicinal Chemistry|January 23, 2024
Correction to "Structure-Activity Relationship of Truncated 2,8-Disubstituted-Adenosine Derivatives as Dual A<sub>2A</sub>/A<sub>3</sub> Adenosine Receptor Antagonists and Their Cancer Immunotherapeutic Activity"Gibae Kim, Xiyan Hou, Woong Sub Byun, et al.
Pageof 60

Showing results (581-590 of 599) with videos related to

Sort By:
Pageof 60
Journal of Medicinal Chemistry|January 25, 2014
Synthesis and anti-renal fibrosis activity of conformationally locked truncated 2-hexynyl-N(6)-substituted-(N)-methanocarba-nucleosides as A3 adenosine receptor antagonists and partial agonistsAkshata Nayak, Girish Chandra, Inah Hwang, et al.
ACS Chemical Neuroscience|September 1, 2021
Discovery of Highly Potent Adenosine A<sub>1</sub> Receptor Agonists: Targeting Positron Emission Tomography ProbesMin Guo, Abolghasem Bakhoda, Zhan-Guo Gao, et al.
Pain|May 8, 2020
Acute visceral pain relief mediated by A3AR agonists in rats: involvement of N-type voltage-gated calcium channelsElena Lucarini, Elisabetta Coppi, Laura Micheli, et al.
ACS Pharmacology & Translational Science|September 19, 2025
P2Y<sub>14</sub> Receptor Antagonists: Piperidine Bioisosteres and Mutagenesis-Supported Molecular ModelingAsmita Pramanik, Zhiwei Wen, Matteo Pavan, et al.
Ophthalmology|March 23, 2010
Treatment of dry eye syndrome with orally administered CF101: data from a phase 2 clinical trialIsaac Avni, Hanna J Garzozi, Irina S Barequet, et al.
Nature Chemistry|October 19, 2023
Stereocontrolled access to thioisosteres of nucleoside di- and triphosphatesHai-Jun Zhang, Michał Ociepa, Molhm Nassir, et al.
Journal of Medicinal Chemistry|December 7, 2011
Structure-activity relationships of truncated C2- or C8-substituted adenosine derivatives as dual acting A₂A and A₃ adenosine receptor ligandsXiyan Hou, Mahesh S Majik, Kyunglim Kim, et al.
Nature|March 28, 2014
Structure of the human P2Y12 receptor in complex with an antithrombotic drugKaihua Zhang, Jin Zhang, Zhan-Guo Gao, et al.
Journal of Medicinal Chemistry|August 21, 2023
Structure-Activity Relationship of Truncated 2,8-Disubstituted-Adenosine Derivatives as Dual A<sub>2A</sub>/A<sub>3</sub> Adenosine Receptor Antagonists and Their Cancer Immunotherapeutic ActivityGibae Kim, Xiyan Hou, Woong Sub Byun, et al.
Journal of Medicinal Chemistry|January 23, 2024
Correction to "Structure-Activity Relationship of Truncated 2,8-Disubstituted-Adenosine Derivatives as Dual A<sub>2A</sub>/A<sub>3</sub> Adenosine Receptor Antagonists and Their Cancer Immunotherapeutic Activity"Gibae Kim, Xiyan Hou, Woong Sub Byun, et al.
Pageof 60