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Chemical compound From Wikipedia, the free encyclopedia
Cinaciguat (BAY 58-2667) is an experimental drug for the treatment of acute decompensated heart failure.
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Routes of administration | intravenous (?) |
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Formula | C36H39NO5 |
Molar mass | 565.710 g·mol−1 |
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Cinaciguat activates the soluble guanylate cyclase (sGC) which is a receptor for nitric oxide. This increases biosynthesis of cyclic GMP, resulting in vasodilation.[1]
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