individual isomers of endo bicyclo (2.21) heptyladenosin

摘要

(1R-endo) or (1S-endo)-N-bicyclo[2.2.1]heptyl adenosine and pharmaceutically acceptable acid addition salts having highly desirable antihypertensive properties and unexpected A1 and A2 receptor binding activity, processes for their manufacture and pharmaceutical compositions and methods for using said compounds and compositions.