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GZ-793A
CAS No. : 1356447-90-9
Biological Activity：GZ-793A is an orally active and selective vesicular monoamine transporter-2 (VMAT2) inhibitor, with an Ki of 0.029 µM. GZ-793A inhibits the neurochemical effects of methamphetamine (METH)-induced dopamine release. GZ-793A can be used for research of METH addiction[2][3].
Research Area：Neurological Disease
Targets：Monoamine Transporter
Related Small Molecules:13-Hydroxyisobakuchiol;hENT4-IN-1;Pseudoisocyanine iodide;FFN511;Nisoxetine hydrochloride;Valbenazine tosylate;Radafaxine hydrochloride;FFN200 dihydrochloride;NBI-98782;Vanilpyruvic acid
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