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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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The peptide may carry the same name
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