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Since the ultimate goal of the project was to produce a clinically relevant molecule that could be delivered peripherally but still exhibit pro-cognitive/anti-dementia activity, the effectiveness of both the intraperitoneal and oral delivery routes of dihexa administration were determined using the scopolamine model

6.1.2.2 Primary efficacy results Clinical results demonstrated that compared to placebo, once-daily 10 mg or 25 mg brensocatib significantly extended time to first acute exacerbation

[3] A 2018 follow-up study further characterized 5-Amino-1MQ in cell-based assays and reported the following selectivity profile against other methyltransferases and related enzymes at concentrations up to 600 M: no detectable inhibition of DNMT1, PRMT3, or NAMPT

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