Structure−Activity Relationships of 2-Chloro- N 6 -substituted-4‘-thioadenosine-5‘-uronamides as Highly Potent and Selective Agonists at the Human A 3 Adenosine Receptor

Structure−Activity Relationships of 2-Chloro- N 6 -substituted-4‘-thioadenosine-5‘-uronamides as Highly Potent and Selective Agonists at the Human A 3 Adenosine Receptor

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Veröffentlicht in:Journal of medicinal chemistry 2006-01, Vol.49 (1), p.273-281
Hauptverfasser: Jeong, Lak Shin, Lee, Hyuk Woo, Jacobson, Kenneth A., Kim, Hea Ok, Shin, Dae Hong, Lee, Jeong A, Gao, Zhan-Guo, Lu, Changrui, Duong, Heng T., Gunaga, Prashantha, Lee, Sang Kook, Jin, Dong Zhe, Chun, Moon Woo, Moon, Hyung Ryong
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container_title Journal of medicinal chemistry
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creator Jeong, Lak Shin
Lee, Hyuk Woo
Jacobson, Kenneth A.
Kim, Hea Ok
Shin, Dae Hong
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Gao, Zhan-Guo
Lu, Changrui
Duong, Heng T.
Gunaga, Prashantha
Lee, Sang Kook
Jin, Dong Zhe
Chun, Moon Woo
Moon, Hyung Ryong
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title Structure−Activity Relationships of 2-Chloro- N 6 -substituted-4‘-thioadenosine-5‘-uronamides as Highly Potent and Selective Agonists at the Human A 3 Adenosine Receptor
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