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Clin Pharmacol Ther ; 99(4): 360-2, 2016 Apr.
Article in English | MEDLINE | ID: mdl-26765222

ABSTRACT

Therapies that modulate cyclic guanosine-3'-5'-monophosphate (cGMP) have emerged as one of the most successful areas in recent drug discovery and clinical pharmacology. Historically, their focus has been on cardiovascular disease phenotypes; however, cGMP's relevance is likely to go beyond this rather limited organ-based set of indications. Moreover, the multitude of targets and their apparent interchangeability is a proof-of-concept of network pharmacology.


Subject(s)
Cyclic GMP/metabolism , Drug Discovery/methods , Enzyme Activators/pharmacology , Phosphodiesterase Inhibitors/pharmacology , Second Messenger Systems/drug effects , Animals , Biomarkers, Pharmacological/metabolism , Enzyme Activation , Enzyme Activators/chemistry , Guanylate Cyclase/metabolism , Humans , Molecular Structure , Phosphodiesterase Inhibitors/chemistry , Receptors, Guanylate Cyclase-Coupled/agonists , Receptors, Guanylate Cyclase-Coupled/metabolism , Structure-Activity Relationship
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