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Medchemexpress LLC Mirodenafil dihydrochloride | 862189-96-6 | 99.1% | 604.59 | 1 ML
SDP

Catalog No. 5000360975
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Mirodenafil dihydrochloride is an orally active, potent, reversible, and selective phosphodiesterase 5 (PDE5) inhibitor. It also functions as a glucocorticoid receptor (GR) modulator and activates the Wnt/β-catenin signaling pathway. It is used in research for conditions such as erectile dysfunction (ED), Alzheimer's disease (AD), and systemic sclerosis (SSc).

  • Exerts neuroprotective functions by activating the cGMP/PKG/CREB signaling pathway.
  • Enhances neuronal survival by protecting mitochondrial membrane potential and inhibiting apoptosis.
  • Inhibits GSK-3β signaling, reducing tau phosphorylation and decreasing Aβ production.
  • Inhibits transcriptional activity and homodimerization of glucocorticoid receptor.
  • Ameliorates dermal fibrosis in SSc mouse models by inhibiting TGF-β signaling pathway.

Catalog No. 50-003-60975 Supplier Medchemexpress LLC Supplier No. HY14930A10MM/1ML
May include imposed supplier surcharges.
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Mirodenafil dihydrochloride is an orally active, potent, reversible, and selective phosphodiesterase 5 (PDE5) inhibitor. It also functions as a glucocorticoid receptor (GR) modulator and activates the Wnt/β-catenin signaling pathway. It is used in research for conditions such as erectile dysfunction (ED), Alzheimer's disease (AD), and systemic sclerosis (SSc).

  • Exerts neuroprotective functions by activating the cGMP/PKG/CREB signaling pathway.
  • Enhances neuronal survival by protecting mitochondrial membrane potential and inhibiting apoptosis.
  • Inhibits GSK-3β signaling, reducing tau phosphorylation and decreasing Aβ production.
  • Inhibits transcriptional activity and homodimerization of glucocorticoid receptor.
  • Ameliorates dermal fibrosis in SSc mouse models by inhibiting TGF-β signaling pathway.

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