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The chemistry and biology of soluble guanylate cyclase stimulators and activators.

Abstract
The vasodilatory properties of nitric oxide (NO) have been utilized in pharmacotherapy for more than 130 years. Still today, NO-donor drugs are important in the management of cardiovascular diseases. However, inhaled NO or drugs releasing NO and organic nitrates are associated with noteworthy therapeutic shortcomings, including resistance to NO in some disease states, the development of tolerance during long-term treatment, and nonspecific effects, such as post-translational modification of proteins. The beneficial actions of NO are mediated by stimulation of soluble guanylate cyclase (sGC), a heme-containing enzyme which produces the intracellular signaling molecule cyclic guanosine monophosphate (cGMP). Recently, two classes of compounds have been discovered that amplify the function of sGC in a NO-independent manner, the so-called sGC stimulators and sGC activators. The most advanced drug, the sGC stimulator riociguat, has successfully undergone Phase III clinical trials for different forms of pulmonary hypertension.
AuthorsMarkus Follmann, Nils Griebenow, Michael G Hahn, Ingo Hartung, Franz-Josef Mais, Joachim Mittendorf, Martina Schäfer, Hartmut Schirok, Johannes-Peter Stasch, Friederike Stoll, Alexander Straub
JournalAngewandte Chemie (International ed. in English) (Angew Chem Int Ed Engl) Vol. 52 Issue 36 Pg. 9442-62 (Sep 02 2013) ISSN: 1521-3773 [Electronic] Germany
PMID23963798 (Publication Type: Journal Article, Review)
CopyrightCopyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Chemical References
  • Enzyme Activators
  • Pyrazoles
  • Pyrimidines
  • Receptors, Cytoplasmic and Nuclear
  • Guanylate Cyclase
  • Soluble Guanylyl Cyclase
  • riociguat
Topics
  • Drug Discovery
  • Enzyme Activation (drug effects)
  • Enzyme Activators (pharmacology)
  • Guanylate Cyclase (metabolism)
  • Humans
  • Pyrazoles (chemistry, pharmacology)
  • Pyrimidines (chemistry, pharmacology)
  • Receptors, Cytoplasmic and Nuclear (metabolism)
  • Signal Transduction
  • Soluble Guanylyl Cyclase

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