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[DOI] [PMC free article] [PubMed] [Google Scholar] 219.Xu T, et al

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foetida , while the synthetic derivative, acetyl 3-aminoethyl SA, was designed based on the structure of the amorfrutins, as well as the ability of other SA-like compounds to very tightly bind GAPDH and HMGB1, our other newly identified SA/aspirin target ( In parallel, our high-throughput screens used to identify human SABPs uncovered HMGB1