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Non-selective inhibitors of cyclic nucleotide phosphodiesterase
(PDE), such as theophylline, have been used extensively since 1958.
In the decade of the '70s, various PDE isoenzymes were defined
which led to the development of the second generation of PDE
inhibitors. Currently a variety of these new inhibitors are under
test as potential anti-inflammatory drugs. During the past five
years, molecular biology has revealed a superfamily of these
phosphodiesterase isoenzymes. This book summarizes the present
state of knowledge, as well as giving a comprehensive description
of the compounds available. It will be invaluable for everyone who
wants to choose the most suitable PDE inhibitor for their research
or who is dealing with such drugs in a clinical setting.
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