作者
Markus Follmann,Jens Ackerstaff,Gorden Redlich,Frank Wunder,Dieter Lang,Armin Kern,Peter Fey,Nils Griebenow,Walter Kroh,Eva‐Maria Becker‐Pelster,Axel Kretschmer,Volker Geiß,Volkhart Li,Alexander Straub,Joachim Mittendorf,Rolf Jautelat,Hartmut Schirok,Karl‐Heinz Schlemmer,Klemens Lustig,Michael Gerisch,Andreas Knorr,Hanna Tinel,Thomas Mondritzki,H Trübel,Peter Sandner,Johannes‐Peter Stasch
摘要
The first-in-class soluble guanylate cyclase (sGC) stimulator riociguat was recently introduced as a novel treatment option for pulmonary hypertension. Despite its outstanding pharmacological profile, application of riociguat in other cardiovascular indications is limited by its short half-life, necessitating a three times daily dosing regimen. In our efforts to further optimize the compound class, we have uncovered interesting structure-activity relationships and were able to decrease oxidative metabolism significantly. These studies resulting in the discovery of once daily sGC stimulator vericiguat (compound 24, BAY 1021189), currently in phase 3 trials for chronic heart failure, are now reported.