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Bioorganic & Medicinal Chemistry|November 4, 2005
Synthesis of hypermodified adenosine derivatives as selective adenosine A3 receptor ligandsLiesbet Cosyn, Zhan-Guo Gao, Philippe Van Rompaey, et al.
Bioorganic & Medicinal Chemistry Letters|April 8, 2021
Structure activity relationship of 3-nitro-2-(trifluoromethyl)-2H-chromene derivatives as P2Y<sub>6</sub> receptor antagonistsYoung-Hwan Jung, Shanu Jain, Varun Gopinatth, et al.
Bioorganic & Medicinal Chemistry Letters|August 31, 2010
Synthesis and evaluation of 1,2,4-triazolo[1,5-c]pyrimidine derivatives as A2A receptor-selective antagonistsBidhan A Shinkre, T Santhosh Kumar, Zhan-Guo Gao, et al.
Cellular and Molecular Neurobiology|June 27, 2003
P2Y6 nucleotide receptor activates PKC to protect 1321N1 astrocytoma cells against tumor necrosis factor-induced apoptosisSeong G Kim, Zhan-Guo Gao, Kelly A Soltysiak, et al.
Journal of Medicinal Chemistry|June 9, 2009
Functionalized congeners of A3 adenosine receptor-selective nucleosides containing a bicyclo[3.1.0]hexane ring systemDilip K Tosh, Moshe Chinn, Andrei A Ivanov, et al.
Biochemical Pharmacology|March 8, 2003
Tumor necrosis factor alpha-induced apoptosis in astrocytes is prevented by the activation of P2Y6, but not P2Y4 nucleotide receptorsSeong G Kim, Kelly A Soltysiak, Zhan-Guo Gao, et al.
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