Abstract
BACE-1 (β-secretase) has emerged as a promising drug to treat Alzheimer’s disease (AD). BACE-1, an aspartic protease, acts on amyloid precursor protein (APP) prompting the formation and deposition of amyloid-β peptide (Aβ). BACE-1 hindrance has direct ramifications in AD pathology without generally influencing viability. However, inhibition of BACE-1 specifically through in vivo models has introduced numerous issues to the researchers. Since its identification in 2000, inhibitors covering a wide range of auxiliary classes have been structured and created. Advancement in these fields brought about targeted drug therapy that may reduce deposition of Aβ plaque in the brain. Natural product derivatives have always been a potential source of drug discovery process, and they are considered to be safe and economical. Flavonoids are an abundance of naturally delivered BACE-1 inhibitors. Citrus bioflavonoids are distinguished as potential noncompetitive BACE-1 inhibitors. Further, xanthones displayed the hindrance of Aβ conglomeration and BACE-1 activity in vitro and in cells, notwithstanding their radical scavenging and metal chelation capacity. The manuscript has been focused to deliver a refreshed learning with array of phytoextracts and lead molecules with BACE-1 inhibitory potential.
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The authors express gratitude to Assam Down Town University and NEF College of Pharmacy, Assam, for support.
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Bhattacharjee, A., Chakraborty, R., Sen, S. (2021). Plant-Based β-Secretase (BACE-1) Inhibitors: A Mechanistic Approach to Encounter Alzheimer’s Disorder. In: Mandal, S.C., Chakraborty, R., Sen, S. (eds) Evidence Based Validation of Traditional Medicines. Springer, Singapore. https://doi.org/10.1007/978-981-15-8127-4_8
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