Rational design, docking, simulation, synthesis, and studies of small benzothiazole molecules as selective BACE1 inhibitors.

BACE-1 is an encouraging target for the development of AD therapeutics. However, many BACE-1 inhibitors failed clinical trials due to their non-selectivity towards BACE-2 or adverse effects. Herein, a set of 96 benzothiazoles were designed based on the structural features of Atabecestat and Riluzole to find a promising selective BACE-1 inhibitor. Out of the 96 designed compounds, compound showed comparable binding affinity with BACE-1 as compared to Atabecestat, and more selective towards BACE-1 as compared to BACE-2. The BACE-1 docking score of Atabecestat and compound were found to be -7.76 and -7.49, respectively, while their corresponding MM-GBSA ΔG energy were -70.39 and -68.97 kcal/mol. In contrast, the BACE-2 docking score of Atabecestat and compound were found to be -6.24 and -5.32, respectively, while their corresponding MM-GBSA ΔG energy were -56.02 and -43.46 kcal/mol. The strong binding affinity of compound was further validated by 100 ns dynamics study. The physicochemical and pharmacokinetic (ADME) profile of compound predicted it as an excellent orally bioavailable brain-penetrant molecule. To confirm these results, compound was synthesized and spectrally characterized. The selectivity and inhibitory potential (IC) of compound was estimated by BACE-1 and BACE-2 FRET assay. Compound was found to inhibit BACE-1 with IC 121.65 nM, while it was found to be less potent on BACE-2 (IC 480.92 nM), as compared to Atabecestat (BACE-1, IC 13.25 nM and BACE-2, IC 7.15 nM).