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P = 0.0054), both of which control mitochondrial fusion, and a decrease in fission protein DRP1 expression (ca

Purity quantified via High-Performance Liquid Chromatography (HPLC) and identity confirmed by Liquid Chromatography-Mass Spectrometry (LC-MS)

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Design of benzoxathiazin-3-one 1,1-dioxides as a new class of irreversible serine hydrolase inhibitors: discovery of a uniquely selective PNPLA4 inhibitor

Primary literature The foundational pharmacology appears in Wikberg JE et al., Pharmacological Research , 2000, and Cone RD, Nature Neuroscience , 2005 [2][3]