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Bioorganic & Medicinal Chemistry Letters
|
December 15, 2007
Synthesis and structure-activity relationship studies of tyrosine-based antagonists at the human P2X7 receptor
Ga Eun Lee, Bhalchandra V Joshi, Wangzhong Chen, et al.
Journal of Medicinal Chemistry
|
January 5, 2013
5'-Phosphate and 5'-phosphonate ester derivatives of (N)-methanocarba adenosine with in vivo cardioprotective activity
T Santhosh Kumar, Tiehong Yang, Shilpi Mishra, et al.
Medchemcomm
|
August 9, 2019
Pyrazolo[4,3-<i>e</i>][1,2,4]triazolo[1,5-<i>c</i>]pyrimidines to develop functionalized ligands to target adenosine receptors: fluorescent ligands as an example
Stephanie Federico, Enrico Margiotta, Silvia Paoletta, et al.
Current Eye Research
|
September 9, 2005
The cross-species A3 adenosine-receptor antagonist MRS 1292 inhibits adenosine-triggered human nonpigmented ciliary epithelial cell fluid release and reduces mouse intraocular pressure
Hui Yang, Marcel Y Avila, Kim Peterson-Yantorno, et al.
Journal of Medicinal Chemistry
|
December 8, 2006
2-triazole-substituted adenosines: a new class of selective A3 adenosine receptor agonists, partial agonists, and antagonists
Liesbet Cosyn, Krishnan K Palaniappan, Soo-Kyung Kim, et al.
The Journal of Biological Chemistry
|
June 1, 2006
A missense mutation in the seven-transmembrane domain of the human Ca2+ receptor converts a negative allosteric modulator into a positive allosteric modulator
Jianxin Hu, Jiankang Jiang, Stefano Costanzi, et al.
Nature
|
August 7, 2024
Structure of the human dopamine transporter and mechanisms of inhibition
Dushyant Kumar Srivastava, Vikas Navratna, Dilip K Tosh, et al.
Journal of Medicinal Chemistry
|
August 28, 2012
Structural sweet spot for A1 adenosine receptor activation by truncated (N)-methanocarba nucleosides: receptor docking and potent anticonvulsant activity
Dilip K Tosh, Silvia Paoletta, Francesca Deflorian, et al.
Bioorganic & Medicinal Chemistry
|
January 24, 2004
Structure-activity relationships of thiazole and thiadiazole derivatives as potent and selective human adenosine A3 receptor antagonists
Kwan-Young Jung, Soo-Kyung Kim, Zhan-Guo Gao, et al.
Circulation. Heart Failure
|
March 14, 2014
Novel protective role of endogenous cardiac myocyte P2X4 receptors in heart failure
Tiehong Yang, Jian-bing Shen, Ronghua Yang, et al.
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of 60
Search research articles
Search
Showing results (351-360 of 599) with videos related to
Sort By:
Page
of 60
Bioorganic & Medicinal Chemistry Letters
|
December 15, 2007
Synthesis and structure-activity relationship studies of tyrosine-based antagonists at the human P2X7 receptor
Ga Eun Lee, Bhalchandra V Joshi, Wangzhong Chen, et al.
Journal of Medicinal Chemistry
|
January 5, 2013
5'-Phosphate and 5'-phosphonate ester derivatives of (N)-methanocarba adenosine with in vivo cardioprotective activity
T Santhosh Kumar, Tiehong Yang, Shilpi Mishra, et al.
Medchemcomm
|
August 9, 2019
Pyrazolo[4,3-<i>e</i>][1,2,4]triazolo[1,5-<i>c</i>]pyrimidines to develop functionalized ligands to target adenosine receptors: fluorescent ligands as an example
Stephanie Federico, Enrico Margiotta, Silvia Paoletta, et al.
Current Eye Research
|
September 9, 2005
The cross-species A3 adenosine-receptor antagonist MRS 1292 inhibits adenosine-triggered human nonpigmented ciliary epithelial cell fluid release and reduces mouse intraocular pressure
Hui Yang, Marcel Y Avila, Kim Peterson-Yantorno, et al.
Journal of Medicinal Chemistry
|
December 8, 2006
2-triazole-substituted adenosines: a new class of selective A3 adenosine receptor agonists, partial agonists, and antagonists
Liesbet Cosyn, Krishnan K Palaniappan, Soo-Kyung Kim, et al.
The Journal of Biological Chemistry
|
June 1, 2006
A missense mutation in the seven-transmembrane domain of the human Ca2+ receptor converts a negative allosteric modulator into a positive allosteric modulator
Jianxin Hu, Jiankang Jiang, Stefano Costanzi, et al.
Nature
|
August 7, 2024
Structure of the human dopamine transporter and mechanisms of inhibition
Dushyant Kumar Srivastava, Vikas Navratna, Dilip K Tosh, et al.
Journal of Medicinal Chemistry
|
August 28, 2012
Structural sweet spot for A1 adenosine receptor activation by truncated (N)-methanocarba nucleosides: receptor docking and potent anticonvulsant activity
Dilip K Tosh, Silvia Paoletta, Francesca Deflorian, et al.
Bioorganic & Medicinal Chemistry
|
January 24, 2004
Structure-activity relationships of thiazole and thiadiazole derivatives as potent and selective human adenosine A3 receptor antagonists
Kwan-Young Jung, Soo-Kyung Kim, Zhan-Guo Gao, et al.
Circulation. Heart Failure
|
March 14, 2014
Novel protective role of endogenous cardiac myocyte P2X4 receptors in heart failure
Tiehong Yang, Jian-bing Shen, Ronghua Yang, et al.
Page
of 60