Title of article
The design and synthesis of novel adenosine agonists
Author/Authors
P. J. Scammells، نويسنده , , S. P. Baker، نويسنده , , L. Bellardinelli، نويسنده , , R. A. Olsson، نويسنده , , R. A. Russell، نويسنده , , S. A. Knevitt، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 1996
Pages
4
From page
811
To page
814
Abstract
The 2R and 2S-endo isomers of N6-(5,6-epoxynorborn-2-yl)adenosine have been synthesised and shown to be potent agonists for the A1 adenosine receptor. The 2S-endo isomer was equipotent to N6-cyclopentyladenosine and 10- to 12-fold more potent than the 2R-endo isomer.
Journal title
Bioorganic & Medicinal Chemistry Letters
Serial Year
1996
Journal title
Bioorganic & Medicinal Chemistry Letters
Record number
788006
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