Product Information
Vu 590 is a histone deacetylase inhibitor that has been shown to have cardioprotective effects. Vu590 binds to the HAT domain of HDAC and prevents the removal of acetyl groups from histones, which causes an increase in gene expression. It also inhibits the activity of ionophores, which are molecules that transport ions across membranes. Vu 590 binds to ionophore channels and blocks their opening, preventing the flow of ions. This drug also has a number of other effects on dopamine and serotonin release, as well as coexpression with adenosine receptors.
Chemical properties
Technical inquiry about: 3D-IWC98783 Vu 590 dihydrochloride
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