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Journal of Medicinal Chemistry
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June 22, 2017
Utilization of an Active Site Mutant Receptor for the Identification of Potent and Selective Atypical 5-HT<sub>2C</sub> Receptor Agonists
Joseph Carpenter, Ying Wang, Gang Wu, et al.
Bioorganic & Medicinal Chemistry Letters
|
April 10, 2007
CC chemokine receptor-3 (CCR3) antagonists: improving the selectivity of DPC168 by reducing central ring lipophilicity
James R Pruitt, Douglas G Batt, Dean A Wacker, et al.
Biomolecular NMR Assignments
|
August 18, 2020
<sup>1</sup>H, <sup>13</sup>C, and <sup>15</sup>N backbone chemical shift assignments of the apo and the ADP-ribose bound forms of the macrodomain of SARS-CoV-2 non-structural protein 3b
F Cantini, L Banci, N Altincekic, et al.
Journal of Medicinal Chemistry
|
September 11, 2014
Discovery of 5-chloro-4-((1-(5-chloropyrimidin-2-yl)piperidin-4-yl)oxy)-1-(2-fluoro-4-(methylsulfonyl)phenyl)pyridin-2(1H)-one (BMS-903452), an antidiabetic clinical candidate targeting GPR119
Dean A Wacker, Ying Wang, Matthias Broekema, et al.
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Search research articles
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Showing results (171-180 of 174) with videos related to
Sort By:
Page
of 18
You have reached the last page of results.
This site can display upto 174 results.
Journal of Medicinal Chemistry
|
June 22, 2017
Utilization of an Active Site Mutant Receptor for the Identification of Potent and Selective Atypical 5-HT<sub>2C</sub> Receptor Agonists
Joseph Carpenter, Ying Wang, Gang Wu, et al.
Bioorganic & Medicinal Chemistry Letters
|
April 10, 2007
CC chemokine receptor-3 (CCR3) antagonists: improving the selectivity of DPC168 by reducing central ring lipophilicity
James R Pruitt, Douglas G Batt, Dean A Wacker, et al.
Biomolecular NMR Assignments
|
August 18, 2020
<sup>1</sup>H, <sup>13</sup>C, and <sup>15</sup>N backbone chemical shift assignments of the apo and the ADP-ribose bound forms of the macrodomain of SARS-CoV-2 non-structural protein 3b
F Cantini, L Banci, N Altincekic, et al.
Journal of Medicinal Chemistry
|
September 11, 2014
Discovery of 5-chloro-4-((1-(5-chloropyrimidin-2-yl)piperidin-4-yl)oxy)-1-(2-fluoro-4-(methylsulfonyl)phenyl)pyridin-2(1H)-one (BMS-903452), an antidiabetic clinical candidate targeting GPR119
Dean A Wacker, Ying Wang, Matthias Broekema, et al.
Page
of 18