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Numerous compounds have been used to inhibit the activity of endogenous mammalian G6PDH in vitro and/or in vivo such as the naturally occurring adrenal steroid dehydroepiandrosterone (DHEA) 3 , catechin gallates, especially epigallocatechin gallate (EGCG) 4 , chelerythrine (initially a PKC inhibitor) and PP2 (Amino-5-(4-chlorophenyl)-7-(t-butyl)pyrazolo[3,4-d]pyrimidine), primarily a Src kinase family inhibitor 5

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In another study, employing the MPP + PD animal model, the supernatant from human umbilical cord (hUC) MSCs infected by an adenovirus carrying the HGF gene promotes a better regeneration of damaged PD dopaminergic neurons as compared to hUC-MSCs alone

Emergency Seizure and Arrhythmia Protocols: Rapid-acting anticonvulsant for acute seizure control and life-threatening ventricular arrhythmias, especially Torsades de Pointes