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European Journal of Medicinal Chemistry
|
August 10, 2023
Structure activity relationships of 5-HT<sub>2B</sub> and 5-HT<sub>2C</sub> serotonin receptor antagonists: N<sup>6</sup>, C2 and 5'-Modified (N)-methanocarba-adenosine derivatives
Dilip K Tosh, Maggie M Calkins, Marko S Ivancich, et al.
Nucleosides, Nucleotides & Nucleic Acids
|
December 7, 2007
Stereoselective synthesis of 1'-functionalized-4'-thionucleosides
Lak Shin Jeong, Prashantha Gunaga, Hea Ok Kim, et al.
Purinergic Signalling
|
November 25, 2017
Species differences and mechanism of action of A<sub>3</sub> adenosine receptor allosteric modulators
Lili Du, Zhan-Guo Gao, Silvia Paoletta, et al.
Journal of Medicinal Chemistry
|
July 11, 2003
A conformationally locked analogue of the anti-HIV agent stavudine. An important correlation between pseudorotation and maximum amplitude
Yongseok Choi, Clifford George, Maria J Comin, et al.
Journal of Medicinal Chemistry
|
August 26, 2021
Subtle Chemical Changes Cross the Boundary between Agonist and Antagonist: New A<sub>3</sub> Adenosine Receptor Homology Models and Structural Network Analysis Can Predict This Boundary
Yoonji Lee, Xiyan Hou, Jin Hee Lee, et al.
Biochemical Pharmacology
|
April 8, 2022
Kinetic profiling and functional characterization of 8-phenylxanthine derivatives as A<sub>2B</sub> adenosine receptor antagonists
Anna Vlachodimou, Henk de Vries, Milena Pasoli, et al.
Biochemistry
|
June 5, 2007
Probing the binding site of the A1 adenosine receptor reengineered for orthogonal recognition by tailored nucleosides
Krishnan K Palaniappan, Zhan-Guo Gao, Andrei A Ivanov, et al.
European Journal of Medicinal Chemistry
|
November 30, 2021
A<sub>3</sub> adenosine receptor agonists containing dopamine moieties for enhanced interspecies affinity
Dilip K Tosh, Veronica Salmaso, Ryan G Campbell, et al.
Bioorganic & Medicinal Chemistry
|
April 21, 2009
Structure-activity relationships of truncated adenosine derivatives as highly potent and selective human A3 adenosine receptor antagonists
Shantanu Pal, Won Jun Choi, Seung Ah Choe, et al.
The Journal of Organic Chemistry
|
June 18, 2005
Synthesis of novel apio carbocyclic nucleoside analogues as selective a(3) adenosine receptor agonists
Jeong A Lee, Hyung Ryong Moon, Hea Ok Kim, et al.
Page
of 60
Search research articles
Search
Showing results (511-520 of 599) with videos related to
Sort By:
Page
of 60
European Journal of Medicinal Chemistry
|
August 10, 2023
Structure activity relationships of 5-HT<sub>2B</sub> and 5-HT<sub>2C</sub> serotonin receptor antagonists: N<sup>6</sup>, C2 and 5'-Modified (N)-methanocarba-adenosine derivatives
Dilip K Tosh, Maggie M Calkins, Marko S Ivancich, et al.
Nucleosides, Nucleotides & Nucleic Acids
|
December 7, 2007
Stereoselective synthesis of 1'-functionalized-4'-thionucleosides
Lak Shin Jeong, Prashantha Gunaga, Hea Ok Kim, et al.
Purinergic Signalling
|
November 25, 2017
Species differences and mechanism of action of A<sub>3</sub> adenosine receptor allosteric modulators
Lili Du, Zhan-Guo Gao, Silvia Paoletta, et al.
Journal of Medicinal Chemistry
|
July 11, 2003
A conformationally locked analogue of the anti-HIV agent stavudine. An important correlation between pseudorotation and maximum amplitude
Yongseok Choi, Clifford George, Maria J Comin, et al.
Journal of Medicinal Chemistry
|
August 26, 2021
Subtle Chemical Changes Cross the Boundary between Agonist and Antagonist: New A<sub>3</sub> Adenosine Receptor Homology Models and Structural Network Analysis Can Predict This Boundary
Yoonji Lee, Xiyan Hou, Jin Hee Lee, et al.
Biochemical Pharmacology
|
April 8, 2022
Kinetic profiling and functional characterization of 8-phenylxanthine derivatives as A<sub>2B</sub> adenosine receptor antagonists
Anna Vlachodimou, Henk de Vries, Milena Pasoli, et al.
Biochemistry
|
June 5, 2007
Probing the binding site of the A1 adenosine receptor reengineered for orthogonal recognition by tailored nucleosides
Krishnan K Palaniappan, Zhan-Guo Gao, Andrei A Ivanov, et al.
European Journal of Medicinal Chemistry
|
November 30, 2021
A<sub>3</sub> adenosine receptor agonists containing dopamine moieties for enhanced interspecies affinity
Dilip K Tosh, Veronica Salmaso, Ryan G Campbell, et al.
Bioorganic & Medicinal Chemistry
|
April 21, 2009
Structure-activity relationships of truncated adenosine derivatives as highly potent and selective human A3 adenosine receptor antagonists
Shantanu Pal, Won Jun Choi, Seung Ah Choe, et al.
The Journal of Organic Chemistry
|
June 18, 2005
Synthesis of novel apio carbocyclic nucleoside analogues as selective a(3) adenosine receptor agonists
Jeong A Lee, Hyung Ryong Moon, Hea Ok Kim, et al.
Page
of 60